Jobs in Somerville New Jersey

276 positions found — Page 3

Sales & Events Coordinator
✦ New
Salary not disclosed
Piscataway, NJ 1 day ago

About

is the premier career networking resource for the Pharmaceutical, Biotechnology, and Medical Device industries. We are looking for a highly organized Sales & Event Operations Coordinator to provide critical administrative support to our sales team and manage the logistical "heavy lifting" for our industry-leading career fairs and events.

The Role

This is a high-impact administrative role designed for a detail-oriented professional who loves organization. You will not be responsible for making sales; instead, you will be the backbone of the departmentβ€”ensuring that once a sale is made, the client is onboarded perfectly and the event logistics are executed flawlessly.

Key Responsibilities

Event & Logistics Support:

  • Vendor Management: Coordinate with venues and vendors for catering & decorating.
  • Exhibitor Onboarding: Send "Welcome" kits to registered companies, collect their logos/bios, and ensure they have everything they need for event day.
  • Onsite Support: Serve as the "Command Center" during live eventsβ€”managing check-ins, distributing badges, and assisting exhibitors with booth setup.
  • Materials Management: Maintain and organize event supplies, marketing collateral, and shipping logistics for regional shows.

Sales & Administrative Operations:

  • Contract Administration: Prepare and send out sales agreements and invoices following client commitments.
  • CRM Maintenance: Keep our client database (CRM) up to date, ensuring all contact information and deal statuses are accurate.
  • Reporting: Generate weekly reports for management on event registration numbers and sales pipeline progress.
  • Lead Management: Organically route incoming inquiries to the sales team and manage the general info@ email account.

Qualifications

  • Organization: You have a "black belt" in multitasking and never let a deadline slip through the cracks.
  • Experience: 2+ years in an administrative, office management, or coordinator role.
  • Communication: Professional and polished; you will be interacting with HR leaders from some of the world’s largest pharma companies.
  • Software Skills: Proficiency in Microsoft Office (Excel is a must), CRM platforms, and ideally some familiarity with event software like Eventbrite or Cvent.
  • Location: Must be able to work onsite daily at our Piscataway, NJ office.

Why ?

  • Stable, Fast-Paced Environment: A professional office setting within the heart of the New Jersey life sciences corridor.
  • Impact: You’ll see the direct results of your work as thousands of professionals find jobs through the events you help build.
  • Team Focus: You are the essential partner to our sales and leadership teams.


$40K Salary

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Contract, Drug Metabolism and Pharmacokinetics (DMPK)
✦ New
🏒 EPM Scientific
Salary not disclosed
Somerset, NJ 1 day ago

Contract DMPK Scientist


A leading biopharmaceutical organisation is seeking an experienced Contract Scientist - Drug Metabolism & Pharmacokinetics (DMPK) to support discovery and early development programmes. This role is suited to candidates with strong hands‑on laboratory experience and a solid background in conducting DMPK studies.


Please note: demonstrated, practical DMPK experience is essential. Applicants without direct DMPK laboratory experience cannot be considered.


Key Responsibilities

  • Conducting established in vitro and in vivo metabolism and bioanalysis assays
  • Operating, troubleshooting, and maintaining LC‑MS/MS systems
  • Supporting the development and optimisation of DMPK assays
  • Analysing, interpreting, and documenting experimental data for internal project teams
  • Recording study details in laboratory systems and preparing technical reports
  • Ensuring adherence to safety guidelines, regulatory requirements, and internal SOPs
  • Contributing to general laboratory operations, including equipment maintenance and capital equipment planning


Required Experience & Qualifications

  • MSc in Biology, Chemistry, Biochemistry, Pharmaceutical Science, Pharmacology or related discipline with 2+ years of relevant experience, OR BSc in the same fields with 4+ years of relevant industry experience
  • Proven experience in DMPK assays, including: Metabolic stability in microsomes and hepatocytes, CYP inhibition and induction assays, Bioanalysis in various biological matrices
  • Hands‑on experience with LC‑MS instruments and automated liquid handling systems
  • Strong understanding of DMPK principles and laboratory methodologies


Additional Skills

  • Excellent analytical, problem‑solving, and organisational abilities
  • Strong written and verbal communication skills
  • Ability to manage multiple projects in a fast‑paced, matrixed environment
  • Proficiency with Microsoft Office
  • Ability to work both independently and collaboratively
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Call Center Specialist
✦ New
🏒 Robert Half
Salary not disclosed

Responsibilities

  • Handle a high volume of incoming calls, live chats, and emails with accuracy and professionalism.
  • Serve as the first point of contact for patients and clients; clearly explain services, policies, and procedures.
  • Gather details, research solutions, and provide accurate information to resolve questions and concerns.
  • Escalate clinical or medical‑related inquiries to appropriate healthcare professionals when needed.
  • Schedule and manage patient appointments following established guidelines.
  • Maintain accurate records of all interactions, appointments, and follow‑up steps.
  • Use medical software and related technology to process scheduling and client requests.
  • Partner with team members to ensure smooth workflow and a positive patient/client experience.

Qualifications

  • Previous healthcare industry experience required.
  • Strong computer skills; proficiency in Microsoft Office.
  • Typing speed of 45+ WPM.
  • Experience with medical scheduling systems or EMR tools preferred.
  • Solid understanding of office procedures and office equipment.
  • Ability to manage high-volume communication across multiple channels with accuracy.
  • Must be able to work onsite, 5 days a week, with a patient‑focused and professional attitude.

Shift Details

  • Standard hours: 7:00 AM – 7:00 PM (8‑hour shifts).
  • Optional early start shifts: 5:00 AM or 6:00 AM.

****MUST HAVE EXPERIENCE IN HEALTHCARE INDUSTRY HANDLING HIGH VOLUME***********



All applicants applying for U.S. job openings must be legally authorized to work in the United States. Benefits are available to contract/temporary professionals, including medical, vision, dental, and life and disability insurance. Hired contract/temporary professionals are also eligible to enroll in our company 401(k) plan. Visit for more information.

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Calibration Technician
✦ New
🏒 Pharma
Salary not disclosed
Warren, NJ 1 day ago

JOB TITLE: Calibration Technician

Location: Warren, NJ (100% onsite)

Duration: 12 months initial (Possibility of extension for the right candidate depending on performance)



Responsibilities:

The duties/responsibilities shall include but not limited to the following:

β€’ Executes equipment calibration, preventative maintenance, performance verification, troubleshooting and repair activities in laboratory and manufacturing areas, as required per current scheduling (CMMS) System.

β€’ Escorts and supervises vendors for calibration, preventative maintenance, performance verification and repair functions as required per current scheduling (CMMS) System.

β€’ Reviews and approves vendor executed calibration, maintenance, repair, and performance verification records for accuracy, and completeness.

β€’ Documents and populates calibration/maintenance information in WPT (Work Plan Template) or MDT (Measurement Data Template) using CMMS system.

β€’ Modifies or update CMMS documentation as required.

β€’ Prepares reports and keeps records on calibration inspection, testing, and repairs.

β€’ Executes requalification on Controlled Temperature Units (ex. Refrigerators, Freezers (which includes -20Β°C / -80Β°C Freezers), Incubators, Cryotanks, Cryopods, and Storage Rooms/Areas).

β€’ Supports multiple sites within Warren.

β€’ Supports clinical manufacturing on-call equipment troubleshooting activities during weekends as required.

β€’ Ensures all calibration, PM, and performance verification records are filed appropriately after approval.

β€’ Contacts supplier for quotation on external calibration/PM of the equipment and calibration standards

β€’ Initiates, participates, and assists in resolution of quality investigations.

β€’ Authors and supports the development, revision, and review of written Standard Operating Procedures (SOP) for calibration, preventive maintenance, and performance verification of instruments/equipment.

β€’ Supports the development, review and approval of calibration and maintenance plans in site CMMS system.

β€’ Supports the execution of process improvement studies, as required.

β€’ Adheres to written policies and procedures governing the LSM department activities and the equipment they manage to ensure compliance with approved standards.

β€’ Performs inventory of the equipment and/or standards in the labs as required.

β€’ Maintains a positive relationship with the site customers and outside vendors while promoting a positive team environment.

β€’ Participates actively in special projects as required.

β€’ Ensure low cost of the Laboratory Systems Management (LSM) department (Reducing overtime, implementing innovative ideas)

β€’ Plans, justify and implement cost reduction small projects.

β€’ Usage of several test equipment and tools (e.g., pressure gauges, temperature, humidity meters, flow meters, particle counters and temperature mapping equipment etc.)

β€’ Follows cGMP (current Good Manufacturing Practices) and ALCOA principles ('ALCOA' defines that data should be Attributable, Legible, Contemporaneous, Original, and Accurate) In addition, 'ALCOA+' guidance recommends that data is also Complete, Consistent, Enduring, and Available.

Inventory Management

β€’ Work with Planning group to ensure system is updated as calibration, maintenance and performance verification activities are performed.

β€’ Supports deviations and investigations that result from calibration or performance verification activities, along with developing and supporting the implementation of corrective and preventive actions.


Regulatory Responsibilities

β€’ Maintains all required Corporate, Facilities and EHS training as required.

β€’ Adheres to all safety procedures and hazard communication.

β€’ May be called upon to act as SME in both internal and regulatory audits.


Qualifications:

Β§ Knowledge of cGMP and good documentation practices.

Β§ Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment.

Β§ Strong problem-solving skills and the ability to work independently.

Β§ Excellent interpersonal and communication skills with experience dealing with a diverse workforce where individual initiative, accountability to the team, and professional maturity are required.

Β§ Strong multi‐tasking and organizational ability. Ability to effectively manage multiple tasks and activities simultaneously.

Β§ Proficiency in Microsoft Office Suite – Word, Excel, PowerPoint, and Outlook; innate ability to learn new software, such as corporate intranet and enterprise applications.

Β§ Working knowledge of scheduling software and systems, and inventory management systems, e.g., Blue Mountain RAM and/or Maximo Computerized Maintenance Management System (CMMS) preferred.

Β§ Ability to interact effectively with QC, Manufacturing, QA, and Engineering & Facilities groups.

β€’ High school Diploma or Associates, or Bachelor's degree.

β€’ Minimum 3 years of experience in FDA-regulated industry.

β€’ Minimum 3 years of experience working directly with laboratory equipment (ex. centrifuges, temperature/humidity meters, balances, freezers, refrigerators etc.)

β€’ Maintenance coordination / planning experience preferred.

Experience working in a clinical environment preferred.


WORKING CONDITIONS:


Environmental Conditions:

β€’ Environment may include working in office, laboratory, or manufacturing area.

β€’ Donning proper gowning and/or PPE such as safety glasses and shoes in an environment with hazardous materials and waste will be required.

β€’ Working safely and effectively when working alone or working with others will be required.

β€’ Local travel is required for this position to support multiple sites.


If hired, you will enjoy the following Eclaro Benefits:

  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro


If you feel you are qualified with the required skills and if you are interested, please free to send your word version most updated resume TAILORED to the job description above to or call (212)804-7476.



Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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Quality Compliance Specialist
✦ New
Salary not disclosed
Somerset, NJ 1 day ago

*Duration: 7 months contract


Job Description:

  • The Quality Analyst is responsible for the oversight and execution of Quality Management Systems and compliance at the Distribution Center. The Quality Analyst serves as a single point of contact to the Sr. Manager, Janssen Commercial Quality and Supply Chain partners on compliance related matters and is the liaison with multiple Quality and Compliance organizations to drive timely resolution of quality and compliance related issues. The Quality Analyst identifies business issues, identifies opportunities to continuously improve quality and compliance and leads improvement opportunities and problem solutions. The Quality Analyst implements and executes quality and compliance programs to ensure effective and consistent processes with established standards.


Responsibilities:

  • Quality and compliance product receiving process, including, but not limited to receiving inspection activities such as review of temperature monitoring devices and systematic transactions in Warehouse Management System and/or SAP
  • Monitoring and following Quarantine/Hold/Stop-Ship/Recall processes and notices
  • Product refusals process activities, including, but not limited to inspection and disposition
  • Serve as single point of contact to internal and external partners on Distribution Quality related matters and liaise with multiple Quality organizations to drive timely resolution of Quality related issues
  • Responsible for adherence to the Deviation, Corrective and Preventative Action (CAPA), and Change Controls processes and Quality Management Systems
  • Responsible for adherence to the Records Management and Retention processes
  • Responsible for adhering to the Training process
  • Supporting internal and external audits
  • Plans, support, and coordinates quality and compliance programs designed to ensure effective and consistent processes with established standards by performing the duties personally
  • Provide quality and compliance oversight for execution of Protocols
  • Notify/escalate critical quality issues to management in a timely manner
  • Provide data/information/metrics to management for Quality System Management Reviews
  • Develop and review of Standard Operating Procedures (SOPs), Work Instructions (WI) and other documents, as needed
  • Drives innovation within functional areas while ensuring functional initiatives are delivered in a compliant and safe manner
  • Identifies opportunities to continuously improve quality, cost and time factors, consistent with both Janssen Commercial Quality and DELIVER Supply Chain business objectives
  • Identify business issues, communicates to management, prioritizes for action, and leads improvement opportunities and problem solutions in collaboration with other Supply Chain partners.
  • Perform gap assessments in local procedures to client Global Standards, Business processes, and External Standards
  • Support of New Product Launch activities at the Distribution Center, including, but not limited to Master Data (sIDMa) set-up
  • Ensures compliance and remaining current with local, state, federal, and international regulations and standards
  • Evaluate the overall compliance risk and recommending corrective actions and tracking progress
  • Responsible for making quality decisions based upon assessments of compliance risks balanced with the overall business needs
  • Compliance oversight for the end-to-end clinical supply chain processes, including, but not limited to re-stickering and other labeling activities
  • Compliance oversight for the end-to-end Re-Pack-Re-Label processes, including, but not limited to Batch Record/Protocol activities
  • Monitor and review temperature data for the Distribution Center and ancillary areas
  • Supports 24/7 operations of the Distribution Center
  • Operate in a team-based environment with minimum supervision
  • Provide training to new hires (FTEs) and/or Contractors
  • Interface collaboratively with other business partners and stakeholders


Experience:

  • A minimum of 2 years of experience in a highly regulated industry is required.
  • Quality and Compliance experience in the Medical Device, Pharmaceutical or Consumer products industry and experience in distribution is preferred.
  • Strong communication, teamwork, problem solving, decision-making, and root cause analysis skills are required.
  • Experience with Warehouse Management Systems and SAP is preferred.
  • Experience with Quality Management Systems such as COMET is preferred.
  • Proficiency in organizational and project management skills is preferred.
  • Experience with Temperature Control is preferred.
  • This position may require up to a 10% of domestic travel.
  • Location can be Shepherdsville, KY or Somerset, NJ


Skills:

  • Quality Management system


Education:

  • A minimum of bachelor’s degree in an Engineering, Life Science, and Technical scientific or related discipline is preferred. In absence of a bachelor’s degree, special consideration would be considered for individuals who have related and background experience.


About US Tech Solutions:

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.


Recruiter Details:

Name: Azhar

Email:

Internal Id: 26-04181

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Senior Sales Operations Analyst
✦ New
Salary not disclosed
Basking Ridge, NJ 1 day ago

Senior Analyst, Sales Operations, Basking Ridge, NJ

Who We Are

Aucta Pharmaceuticals is an emerging product development pharmaceutical company.We are on our way to becoming a significant specialty pharmaceutical company in the U.S. marketplace integrating R&D, manufacturing, and commercialization. We focus on improved dosage forms for patients with a therapeutic focus in CNS and select orphan drug disease states.


Aucta successfully launched its first branded product, Motpoly XR, in the epilepsy space with a targeted sales force in March 2024 and an expanded presence of 20 field sale territories and 3 inside sales positions in late 2024. Our objective is to enhance our marketing, managed care, and sales capabilities to support future pipeline products in neurology over the coming years.

Position Description


The Senior Analyst, Sales Operations, is a key member of Aucta’s Commercial Operations team and plays a critical role in enabling sales effectiveness, operational execution, and data-driven decision-making across the organization.


This role serves as the primary point of contact and vendor manager for core Sales Operations platforms, including Veeva CRM, MMIT, and Power BI, and is responsible for managing core quarterly commercial processes such as Incentive Compensation updates, targeting changes, sales force size and structure adjustments, and system governance.


In addition, this position leads the development and maintenance of training materials and delivers training for both field and inside sales and home office teams across Commercial Operations tools and platforms.


This is a highly visible, hands-on role in a fast-growing environment that requires strong analytical skills, operational rigor, comfort working cross-functionally, and the ability to translate complex data and systems into clear, actionable guidance for the business.


The role reports to the Director of Sales Operations.

Primary Responsibilities:

Sales Operations & Vendor Management

  • Serve as the primary point of contact and internal owner for Sales Operations tools and vendors, including Veeva CRM, MMIT, Power BI, and related commercial analytics platforms.
  • Manage vendor relationships, system enhancements, issue resolution, upgrades, and roadmap discussions to ensure tools meet evolving business needs.
  • Partner with IT, Finance, Sales leadership, and external vendors to maintain data integrity, system performance, and compliance.

Commercial Process Management

  • Own and manage the quarterly change process for:
  • Incentive compensation plan updates and calculations
  • Targeting and call plan changes
  • Sales force size, structure, and territory adjustments
  • Ensure timely, accurate execution of all changes and clear communication with stakeholders.
  • Support forecasting, goal setting, and sales performance tracking activities.

Analytics & Reporting

  • Utilize advanced Excel, SQL, and Power BI to analyze sales performance, trends, and operational KPIs.
  • Build, maintain, and enhance dashboards and reports to support Sales leadership, Commercial Operations, and Executive leadership.
  • Partner cross-functionally to translate business questions into data-driven insights.


Training & Enablement

  • Develop, maintain, and continuously improve training materials (guides, SOPs, slide decks, job aids) for Sales Operations tools and processes.
  • Conduct training sessions for field and inside Sales and home office associates on:
  • Veeva CRM functionality and best practices
  • MMIT data usage and interpretation
  • Power BI dashboards and reporting
  • Other Commercial Operations platforms as needed
  • Serve as a trusted resource for ongoing user support and best-practice guidance.

Cross-Functional Support

  • Collaborate closely with Sales, Marketing, Managed Care, Finance, and leadership to support commercial execution.
  • Participate in sales meetings, planning sessions, and plan-of-action meetings as needed.
  • Identify opportunities for process improvement, automation, and scalability as the organization grows.

Required Qualifications

  • Bachelor’s degree in Business Administration, Finance, Analytics, Information Systems, or a related field.
  • 3-5+ years of experience in Sales Operations, Commercial Operations, or analytics roles, preferably within the pharmaceutical or healthcare industry.
  • Hands-on experience with Veeva CRM, MMIT, and Power BI strongly preferred.
  • Advanced proficiency in Microsoft Excel (including complex formulas and data modeling); SQL experience preferred.
  • Strong understanding of sales force structure, targeting, incentive compensation, and CRM processes.
  • Demonstrated ability to manage vendors and cross-functional stakeholders.
  • Strong communication and training skills, with the ability to explain technical concepts to non-technical audiences.
  • Highly organized, detail-oriented, and able to manage multiple priorities in a fast-paced environment.
  • Proactive, collaborative team player with a strong sense of ownership and accountability.

Work Location:

This position is based at our Basking Ridge, NJ site. It is an office-based role, requiring presence 5 days a week. The selected candidate must be able to commute to Basking Ridge, NJ



Salary Range

Aucta Pharmaceuticals considers a combination of education, experience, internal equity, and external market data when determining compensation.

  • Base Salary: $80,000 – $110,000 (commensurate with experience)
  • Bonus Incentive: 10%


Benefits

Aucta offers a competitive benefits package, including:

  • Medical, Dental, and Vision Insurance
  • 401(k)
  • Life Insurance
  • Short- and Long-Term Disability
  • Paid Time Off (PTO)


Aucta Pharmaceuticals is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.


Please refrain from forwarding unsolicited resumes from agencies to Aucta Pharmaceuticals. Aucta is not liable for any fees incurred from the use of resumes from this source. We only compensate agencies with whom we have a formal agreement. For recruitment inquiries, please reach out directly through this post

Applications will be accepted until the position is filled.

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Data Entry Clerk
✦ New
🏒 TSR Consulting
Salary not disclosed

Job Responsibilities:

β€’ Review client/insured data from one proprietary main frame system and transfer data to a second proprietary main frame system.

β€’ Compile and verify the accuracy of data before it is entered.

β€’ This includes ensuring accurate entry of existing data along with the ability to apply the appropriate/ matching additional coverages.

β€’ Individual needs to be able to represent the company in addressing referral reasons/instances with agents and internal customers.

β€’ Within 90 days of hire, reach a quality goal of 80% (with further progression to 95% within 150 days). At the same time, reach an established production goal of 60% within 90 days of higher (with further progression to 90% within 150 days. Review and correct any errors within 24hours of return from the team specialist and/or trainer.

Skills:

β€’ Technical skills include Windows 10 operating platform; ability to research policy information from one proprietary mainframe and system and enter the data into a second proprietary system. A basic operating understanding of Microsoft Office tools (Outlook, Excel, Access and Word) as these tools are used in our daily processes for email communication and tracking. This would not include creation of new spreadsheets or tracking forms as tools are pre-existing. The individual will need to update existing tracking documents to manager their assigned work as well as managing their calendar.

β€’ Verbal and written communication skills, attention to detail, and interpersonal skills.

β€’ Individual will need to accurately document data and follow established process procedures with a general understanding of where to locate all information necessary to complete the process.

β€’ Must be able to multi-task and follow procedures.

β€’ Ability to work both independently and as an engaged member of the team; and manage ones time.


Education/Experience

β€’ Previous experience with:

o Windows 10 operating system.

o Working knowledge of Microsoft Word (how to create Word Document and attach to an email).

o Basic understanding of a pre-existing Excel spreadsheet.

β€’ computers and applications such as Microsoft Word and Excel. Please be specific on what knowledge is needed for Work and Excel


β€’ Education/Experience: High school diploma or GED required.

β€’ Minimum 2 years of office / business experience. Personal Lines Insurance knowledge and plus.


Education/Experience

β€’ Previous experience with:

o Windows 10 operating system.

o Working knowledge of Microsoft Word (how to create Word Document and attach to an email).

o Basic understanding of a pre-existing Excel spreadsheet.

β€’ computers and applications such as Microsoft Word and Excel. Please be specific on what knowledge is needed for Work and Excel

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Human Resources Payroll Manager
✦ New
Salary not disclosed
Somerville, NJ 1 day ago

About the Opportunity


We are seeking an experienced and detail-oriented HR and Payroll Manager to oversee payroll processing and human resources operations across multiple related business entities. This role is responsible for ensuring accurate payroll administration, benefits coordination, regulatory compliance, and maintaining organized and compliant HR records.


This is an excellent opportunity for a hands-on HR and payroll professional who thrives in a structured, collaborative environment and enjoys supporting both employees and leadership.

Key Responsibilities


Payroll Administration

  • Process accurate weekly payroll for a multi-entity workforce, ensuring proper job and department coding
  • Administer payroll for both union and non-union employees
  • Submit certified payroll reports and ensure compliance with applicable wage regulations
  • Coordinate with external partners supporting payroll tax filings and compliance activities
  • Maintain payroll records and ensure accuracy and timeliness


Human Resources Operations

  • Manage full-cycle HR functions including recruiting, onboarding, and employee separations
  • Maintain accurate and compliant employee records and HR documentation
  • Coordinate employee benefits enrollments, changes, and reconciliations
  • Track employee certifications, training, and compliance requirements


Compliance and Reporting

  • Ensure HR practices align with federal, state, and regulatory requirements
  • Support compliance reporting, documentation tracking, and internal audits
  • Maintain HR metrics, reporting accuracy, and workforce records


Collaboration and Support

  • Partner closely with finance and leadership to support payroll and HR initiatives
  • Communicate proactively regarding payroll, compliance, and employee-related matters
  • Contribute to process improvements and operational efficiency


Qualifications

  • 5+ years of HR and payroll experience required
  • Experience processing weekly payroll required
  • Experience supporting union and non-union payroll environments strongly preferred
  • Construction, contracting, or project-based workforce experience is a plus
  • Strong analytical skills and high attention to detail
  • Excellent communication and interpersonal skills
  • Ability to work independently and collaboratively
  • Strong organizational and data management capabilities


Compensation & Benefits

  • Competitive salary
  • Medical, Dental, and Vision Insurance
  • 401(k) retirement plan
  • Paid Time Off and company holidays
  • Collaborative and professional work environment


Ascendo is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability.

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Health Safety Environment Coordinator
✦ New
Salary not disclosed
Branchburg, NJ 1 day ago

EHS Coordinator


Scope of Work / Job Description


The resource(s) will independently act as the Specialist User Representative to support the identification of energy isolation points. Using these isolation points, the resource will create Energy Control Plans (ECPs) within the site’s Lockout/Tagout (LOTO) program using the Link360 ProcessPlus software system.


Support Responsibilities Include:

  • Assist Plant (PLT) and Process Engineering (PE) teams in creating LOTO isolation points, associated metadata, and ECPs in Link360 ProcessPlus.
  • Review equipment P&IDs to ensure all isolation points (manual valves, steam traps, instruments, etc.) within the LOTO boundary are identified and accurately documented.
  • Convert existing (legacy) ECP forms into new ECPs within Link360 ProcessPlus:

Based on the isolation points database


In collaboration with Engineering and Maintenance SMEs to ensure ECPs are complete and accurate for the intended tasks


Ensure ECPs are completed and accounted for all applicable assets prior to Go-Live.


Route ECPs for review and approval.


Required Experience and Qualifications

  • Strong computer proficiency and high attention to detail
  • Ability to read and interpret P&IDs
  • Ability to engage and collaborate with site stakeholders to ensure complete and accurate information
  • Experience with Safety and LOTO programs (preferred)

Prior experience in a regulated environment (preferred)

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Human Resources and Payroll Manager
✦ New
🏒 Ascendo Resources
Salary not disclosed
Somerset, NJ 1 day ago
  • Fully onsite role in Somerset, NJ, Monday–Friday with an 8:00am start (no later); confidential hire.
  • Construction industry required.
  • Individual contributor reporting to the CFO and Controller; collaborates with CFO, Controller, HR Manager, AP Manager, and AP Specialist.
  • Oversees A–Z HR and weekly payroll for multiple related construction companies (30–70 employees depending on projects).
  • Processes union and non-union payroll, including certified payroll under the Davis-Bacon Act for prevailing wage projects.
  • Handles weekly, quarterly, and annual payroll tax filings (W-2s, 940, ACA); tax/compliance support is outsourced.
  • Manages union remittances, 401(k) funding, benefit reconciliations, and HR recordkeeping (I-9s, EEO, compliance).
  • Leads recruiting, onboarding, terminations, training coordination, and certification tracking.
  • Analytical, detail-oriented role requiring strong data analysis, accuracy, and communication skills.
  • Minimum 5+ years payroll/HR experience.
  • Base salary up to $125K; best suited for mid-career candidates.


Ascendo is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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Mobile boiler technician
✦ New
🏒 JCMLiving
Salary not disclosed
Piscataway, NJ 1 day ago

Mobile Boiler Technician

Location

Field-based / Multiple Properties

Job Summary

We are seeking a skilled and reliable Mobile Boiler Technician to maintain, service, troubleshoot, and repair boiler systems across a portfolio of residential and/or commercial properties. This role requires strong technical expertise, a safety-first mindset, and the ability to work independently while delivering excellent service to tenants and property managers.

Key Responsibilities

  • Perform routine maintenance, inspections, and repairs on boiler systems (gas, oil, and/or electric)
  • Diagnose mechanical, electrical, and control system issues and complete timely repairs
  • Respond to emergency service calls, including after-hours or on-call rotations
  • Ensure boilers operate safely, efficiently, and in compliance with local codes and regulations
  • Complete combustion analysis, pressure testing, and system performance evaluations
  • Replace or repair valves, pumps, burners, controls, heat exchangers, and related components
  • Maintain accurate service records, work orders, and compliance documentation
  • Communicate clearly with property managers and tenants regarding system status and repairs
  • Identify potential issues and recommend preventative maintenance or system upgrades
  • Maintain tools, equipment, and company vehicle in safe working condition

Qualifications & Experience

  • High school diploma or equivalent (technical or trade school preferred)
  • 3+ years of hands-on boiler maintenance and repair experience
  • Strong understanding of hydronic systems, piping, controls, and combustion
  • Ability to read blueprints, schematics, and technical manuals
  • Valid driver’s license with a clean driving record
  • Ability to work independently and manage multiple service calls

Certifications & Licensing (Preferred or Required)

  • Boiler Operator License or experience


Skills & Competencies

  • Strong troubleshooting and problem-solving skills
  • Excellent time management and organizational abilities
  • Professional customer service and communication skills
  • Physically able to lift equipment, climb ladders, and work in mechanical rooms
  • Comfortable working in occupied residential and commercial environments
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Document Controller
✦ New
Salary not disclosed
Piscataway, NJ 1 day ago

Job Title: Bid Manager / Project Controller

Location: Piscataway, New Jersey

Salary: Up to $110,000 (based on experience)

Full-Time | Competitive Benefits

Join Our Team in Piscataway, NJ

We are seeking a detail-oriented and strategic Bid Manager / Project Controller to join our growing team in Piscataway - the right candidate will be incredibly detail oriented. This role is ideal for a professional who excels at managing bids, overseeing project financials, and ensuring operational excellence from proposal through execution.

With a competitive salary of up to $110,000, this is an excellent opportunity to play a critical role in driving project success and business growth.

Key Responsibilities

  • Excellent and proven attention to detail. The rest can be taught!
  • Lead and coordinate the end-to-end bid and proposal process
  • Prepare cost estimates, pricing models, and financial analyses
  • Develop and maintain project budgets, forecasts, and cost controls
  • Monitor project performance against financial and operational targets
  • Identify risks and implement mitigation strategies
  • Collaborate with engineering, operations, finance, and leadership teams
  • Support contract negotiations and ensure compliance with client requirements
  • Produce detailed reporting for senior management and stakeholders

Qualifications

  • Bachelor’s degree in Business, Finance, Engineering, or related field
  • 3+ years of experience in bid management, project controls, or financial project oversight
  • Strong financial acumen and analytical skills
  • Experience with budgeting, forecasting, and cost tracking
  • Excellent organizational and communication skills
  • Proficiency in Excel and project management software
  • PMP or similar certification (preferred but not required)
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Transaction Coordinator
✦ New
🏒 Robert Half
Salary not disclosed
Warren, NJ 1 day ago

Key Responsibilities

  • Assist with the preparation, organization, and review of commercial closing documents, including loan documents, settlement statements, and closing checklists.
  • Coordinate with attorneys, lenders, title companies, borrowers, brokers, and internal stakeholders to facilitate smooth and timely closings.
  • Track and manage closing timelines, critical dates, and outstanding conditions.
  • Order and follow up on third-party items such as title commitments, surveys, estoppels, certificates of insurance, subordinations, and payoff statements.
  • Review documents for accuracy, completeness, and compliance with transaction requirements.
  • Prepare closing packages and ensure all documents are properly executed, received, and recorded.
  • Maintain organized electronic and physical transaction files in accordance with company policies.
  • Communicate status updates and resolve document or scheduling issues as they arise.
  • Assist with post-closing activities, including document distribution, record retention, and final file audits.
  • Provide general administrative and clerical support to the closing or legal team as needed.


Required Qualifications

  • High school diploma or equivalent required; associate’s or bachelor’s degree preferred.
  • Prior experience in commercial or residential real estate, legal, title, banking, or loan processing strongly preferred.
  • Strong attention to detail with the ability to manage multiple transactions simultaneously.
  • Excellent written and verbal communication skills.
  • Ability to handle confidential and sensitive information with discretion.
  • Proficiency in Microsoft Office applications (Word, Excel, Outlook).


The company will provide Medical insurance, Vision insurance, Dental insurance, 401(k), Paid maternity leave, Paid paternity leave, and other benefits.

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Customer Success Specialist
✦ New
Salary not disclosed
Somerset, NJ 1 day ago

Do you love developing and nurturing great relationships?


As an N2S Customer Success Specialist, you will be responsible for managing and growing our Fortune 500 accounts, understanding their staffing requirements, and ensuring the successful placement of qualified candidates. You will play a crucial role in building strong client relationships and contributing to the growth and success of N2S


Location: Onsite from Somerset,NJ


Qualifications:

  • Must have 3-5 years of overall experience in the Staffing & Recruiting Industry with hands on recruiting experience and exposure of client communication preferably with Life Sciences MSP clients.
  • Strong understanding of working with VMS and MSP based accounts.
  • Any experience working with a Hybrid/Offshore delivery model will be a plus.
  • Proven experience in staffing, recruiting & client communication, supporting client/ MSP programs from a supplier side.
  • Strong interpersonal and communication skills.
  • Excellent negotiation and problem-solving abilities.
  • Excellent reputation and relationship-building skills.
  • Ability to work in a fast-paced, target-driven environment.
  • Must be a self driven and highly motivated individual.
  • Proficiency in using applicant tracking systems (ATS) and other relevant software.


Key Responsibilities:

  • Be the single point of contact for our Fortune 500 clients
  • Build long-term client partnerships to understand their challenges and provide solution.
  • Maximize market share with a client to make us their trusted staffing supplier.
  • Qualify new job orders and work with the delivery lead for better coverage and support.
  • Present candidates to Hiring Managers and follow up for feedback .
  • Coordinate with Client to schedule candidate interviews and onboarding.
  • Coordinate with recruiting team including screening, orientation, and placement of candidates.
  • Use CRM/ATS (Job Diva) to manage activities.
  • Constant communication with clients to build rapport and to obtain critical information including, job descriptions, referrals, and business leads.


Additional Requirements:

  • Must be open to travel across the country, especially locally, and support clients from their offices.
  • Availability to work outside regular office hours, if needed.


Benefits of working at N2S:

  • Uncapped Commissions
  • 100% Contribution to Health/Dental/Vision
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Payroll & Benefits Manager
✦ New
🏒 LHH
Salary not disclosed

Payroll & Benefits Manager (U.S. & Canada)

We are seeking an experienced Payroll & Benefits Manager to lead the accurate, compliant, and timely administration of payroll and employee benefits for approximately 100 employees across the United States and Canada. This role serves as the subject matter expert for payroll processing, benefits administration, and related compliance, while partnering closely with HR, Finance, and external vendors to deliver an excellent employee experience.

Key Responsibilities

Payroll Management

  • Oversee end-to-end payroll processing for U.S. and Canadian employees, including salaried and hourly staff
  • Ensure payroll accuracy, timeliness, and compliance with federal, state/provincial, and local regulations
  • Administer payroll taxes, filings, and remittances (e.g., IRS, CRA, and state/provincial agencies)
  • Reconcile payroll reports, general ledger entries, and benefit deductions
  • Manage year-end processes, including W-2s, T4s, and related reporting
  • Serve as the primary point of contact for payroll vendors and auditors

Benefits Administration

  • Administer employee benefits programs, including health, dental, vision, life insurance, disability, retirement plans, and wellness initiatives
  • Manage benefit enrollments, changes, and terminations for U.S. and Canadian employees
  • Ensure compliance with benefits-related regulations (e.g., ACA, COBRA, ERISA, HIPAA in the U.S.; applicable provincial regulations in Canada)
  • Act as a liaison with benefits brokers and vendors, supporting renewals and plan evaluations
  • Respond to employee payroll and benefits inquiries with professionalism and confidentiality

Compliance & Reporting

  • Maintain compliance with employment laws and payroll/benefits regulations in both countries
  • Monitor legislative changes and recommend process or policy updates as needed
  • Prepare and maintain payroll and benefits documentation, policies, and procedures
  • Support internal and external audits related to payroll and benefits

Systems & Process Improvement

  • Maintain and optimize payroll and HRIS systems
  • Identify opportunities to streamline payroll and benefits processes and improve efficiency
  • Develop and maintain standard operating procedures and internal controls

Collaboration & Support

  • Partner with HR and Finance teams to ensure accurate and aligned employee data
  • Support onboarding and offboarding processes related to payroll and benefits
  • Provide reporting and analysis on payroll costs, benefits utilization, and compliance

Qualifications

  • Bachelor’s degree in Accounting, Finance, Human Resources, or a related field preferred
  • 5–7 years of progressive payroll and benefits experience, including U.S. and Canadian payroll
  • Prior experience managing or supervising payroll staff preferred
  • Strong knowledge of wage and hour laws, payroll tax regulations, and compliance requirements
  • Experience with payroll systems such as ADP Workforce Now, SAP, Workday, or similar platforms
  • Advanced Excel skills and experience with HRIS integrations
  • Exceptional attention to detail, accuracy, and confidentiality
  • Strong analytical, organizational, and problem-solving skills
  • Excellent interpersonal and communication skills

Additional Information

  • Standard work hours: Monday–Friday, 8:00 a.m.–5:00 p.m.
  • Hybrid work arrangement available after the initial training period
  • Salary range: $85,000–$90,000
  • Comprehensive benefits package including medical, dental, vision, 401(k) with company match, generous PTO and sick time, employee fitness program, and more

Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: β€’ The California Fair Chance Act β€’ Los Angeles City Fair Chance Ordinance β€’ Los Angeles County Fair Chance Ordinance for Employers β€’ San Francisco Fair Chance Ordinance

Not Specified
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Manufacturer
Salary not disclosed
Join a dynamic team where your engineering expertise drives real-world results! Schwing Bioset is looking for an Electrical Project Engineer who loves turning complex ideas into successful projects.

You'll work closely with clients, project managers, and a talented engineering team to ensure every project meets specifications, stays on schedule, and stays within budget.

No relocation assistance available for this position.

Not available for hybrid working hours- must live in or around the Somerset WI area.
Not Specified
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Oncology Clinical Educator - New Jersey
Salary not disclosed
Basking Ridge 2 days ago
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines.

With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.

Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.

Job Summary The Oncology Clinical Educator role provides disease state, REMS, and product safety education and training to key healthcare providers within Oncology clinics, and health care providers (HCPs) in both the hospital and clinic/office setting.

The individual will work within a specified region to enhance disease, REMS, and product safety knowledge, coordinate and provide staff training, and enhance proper administration.

The Oncology Clinical Educator (OCE) role is a position that is field based and is comprised of nurses working under the general direction of the Regional Director of Clinical Nurse Managers.

The OCE is responsible for educating HCPs/clinics with infusion and related education for prescribed DSI products.

The OCE serves as the disease state and product safety expert for their assigned territories.

The OCE serves as a resource to clinical leaders by identifying disease state, REMS, and product safety educational needs of staff and implements programs to fulfill knowledge gaps.

This collaborative approach will serve to provide education and enhanced clinical care.

The OCE is bound by the product label for all educational efforts, and in the interaction with non-commercial counterparts.

Excellent organizational, creative and analytical problem solving, communication, and presentation and skills are required.

This individual must be flexible and adaptable to new and constant changing situations.

Responsibilities Provides education to health care professionals about disease states and REMS and product safety information for specified DSI products in the medical community within an assigned geographical area in accordance with DSI general direction and policy, focused on the assigned targeted segments (i.e: Hematology/Oncology, Gastroenterology, Nephrology, Hospital Pharmacy, OB/GYN and Cardiology).

Develops strong, long-term relationships with clinical personnel Ensures appropriate and compliant utilization of product and disease state education as it relates to DSI products.

Executes disease state educational presentations and on label product safety presentations for in-office/in-hospital educational programs to customers that are guided and designed to address clinical knowledge or product gaps.

Must be able to educate and use multiple approaches to explain complex and difficult material and use experiences to illustrate ideas and facilitate understanding while maintaining the ability to stimulate customer interest.

Collaborates to identify and strategizes on how to best educate customers.

Develops and executes geographical based strategic and tactical plans to meet targeted customer needs.

Monitor, collect, and communicate to the Director, Clinical Nurse Manager on customer insights regarding their need for information regarding disease state, REMS and safety information with respect to DSI marketed products.

Collaborate with managed care counterparts or MSLs to provide ongoing clinical updates that are impacted by reimbursement and/or clinical guidelines.

Identifies and contributes to the development of nursing/HCP specific materials to fulfill customer needs to include, but not limited to, patient educational aids, product reference aids and slide deck content topics.

Qualifications Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.

Education Qualifications (from an accredited college or university) Bachelor's Degree required Experience Qualifications 4 or more years in pharma industry preferred, ideally Hematology/Oncology or 3 or more years of healthcare related experience required Experience with infusion nursing experience preferred Ability to travel up to 90% within geography and to required meetings.

Licenses and Certifications RN
- Registered Nurse
- State Licensure and/or Compact State Licensure The ideal candidate will be a Registered Nurse with previous relevant clinical as well as pharmaceutical industry experience calling on different levels of the health care providers (HCPs) in both the hospital and clinic/office setting required Additional Qualifications: Ability to travel up to 90% within geography and to required meetings.

Must have a valid driver's license with a driving record that meets company requirements Compensation and seniority level/title based on experience and qualifications.

Daiichi Sankyo, Inc.

is an equal opportunity/affirmative action employer.

Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range: USD$140,480.00
- USD$210,720.00 Download Our Benefits Summary PDF
Not Specified
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Project Lead, Clinical Supply Chain
🏒 Daiichi Sankyo, Inc.
Salary not disclosed
Basking Ridge 2 days ago
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines.

With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.

Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.

Job Summary This position is responsible for enabling the on-time delivery of clinical supplies across the DSI portfolio.

This role is primarily responsible for supporting CSO Project Management Leads by developing and updating Study Supply Plans, managing various work streams with key service providers and working with internal departments to progress clinical supply projects.

Every effort has been made to identify the essential functions of this position.

However, it in no way states or implies that these are the only duties you will be required to perform, nor is it intended to be such a listing of the skills and abilities required to do the job.

The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or is an essential function of the position.

Responsibilities Develops and updates Study Supply Plans in close communication with CSO project Management Lead Responsible for the Clinical Label Development process which includes creation of master label text, translations, and label proofs.

Manages the packaging Batch Record review and approval process with Quality Assurance and other CSO personnel.

Works closely with Quality Assurance to obtain temperature excursion disposition to update impacted inventory in IRT and other related systems.

Coordinates authorized destruction of investigational products with approved vendors and obtains required documentation.

Vendor Management –supports Person in Plant (PIP) activities when packaging operations for DSI are in-process.

Supports investigational product distribution activities at the vendor, including generation of drug orders, review of shipping documentation and obtaining approval to ship Assists in the creation of SOP’s and work instructions specific to CSO Supply Planning as requested.

Responsible for updating relevant Trial Master Files (TMF) with CSO-related documents Supports the CSO Project Mgmt Lead in executing additional operational and logistical duties as discussed and agreed to by management Qualifications Education Qualifications Bachelor's Degree Bachelor's degree in Science or related field.

Extensive experience will be considered in lieu of an advanced degree required Experience Qualifications 7 or More Years of related experience, including Project Management, Clinical Supply Management, and/or Pharmaceutical Development.

preferred Oncology experience preferred Creation of Supply Planning tools preferred Travel Requirements Ability to travel up to 10% of the time.

Overnight / single-day travel will be required to go to outsourcing vendors from time to time infrequently.

Daiichi Sankyo, Inc.

is an equal opportunity/affirmative action employer.

Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range: USD$116,400.00
- USD$174,600.00 Download Our Benefits Summary PDF
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Director, GOMA Program Management & Operational Excellence
🏒 Daiichi Sankyo, Inc.
Salary not disclosed
Basking Ridge 2 days ago
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines.

With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.

Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.

Job Summary The Global Oncology Medical Affairs (GOMA) Director, Program Management & Operational Excellence provides strategic planning and operational management oversight of GOMA projects, activities, and budgets.

The Director, Program Management & Operational Excellence is responsible for supporting the Head, Program Management & Operational Excellence, the assigned Global Medical Affairs Team (GMAT) or Functional Lead, and the Franchise or Function Head to deliver GOMA projects and activities successfully and in a timely manner while working in a fast-moving, matrixed organization.

The Director, Program Management & Operational Excellence is responsible acting as the "Chief of Staff" for his/her team, leading efforts to achieve overall operational excellence across all activities and projects to accelerate business in a compliant and efficient manner.

The Director, Program Management & Operational Excellence further contributes to accelerating and optimizing the business via the following responsibilities / activities: β€’Leading / contributing to process improvement initiatives β€’Ensuring streamlined and efficient communication β€’Escalating issues in a timely manner β€’Budget management and oversight of contract-to-purchase order (PO) process β€’Facilitating key meetings (internal GMA, cross-functional, cross-regional, vendor meetings, etc.) β€’Tracking of activities in terms of timing, anticipated risk, and mitigation of issues/conflict resolutions β€’Encouraging overall operational excellence across all activities and projects Job Description Responsibilities GMAT/Function Support In close collaboration with the Team Lead (GMAT or Function), establish a strategic plan for monitoring the activities per the Business Plan and priorities.

Support Team Lead to manage GOMA project/activities, including ensuring that the GMAT/Function team delivers projects/activities successfully and on a timely manner as per annual plan & objectives.

Establish milestones and metrics, in collaboration with GMAT/Function team, and develop a detailed project plan in order to track progress and measure impact of the activity.

Generates critical path analyses and supports scenario planning for each GMAT/Function, in order to assess if objectives are met, exceeded, or not met.

Have a strong understanding of activities, associated budget, and key contributing factors in order to anticipate potential risks and establish plan to mitigate, as appropriate.

Lead and facilitate regular internal GOMA & cross-functional/cross-regional team meetings; ensure agendas and team priorities are clear, meetings minutes are distributed, action items are completed.

Lead the budget planning and tracking process for GMAT/Function team; work with GMAT/Function Leads to provide consolidated budget/LE updates (across all activities and regions) in a timely manner with appropriate rationale.

Support GMAT/Function lead with annual Business Planning process & associated documents, including proactive engagement with internal and external stakeholders to manage plan development.

Proactively follow-up on action items and requests of GMAT/Franchise Lead.

Support GMAT/Function/Franchise Head in prioritization and planning of resources and develop rationale for annual resource planning.

Lead issue resolution meetings.

Lead risk identification, prioritization, and mitigation planning processes across the Franchise.

Manage the agendas for GMAT/Function meetings, the conduct of the GMAT/Function meetings, and the drafting of GMAT/Function meeting minutes.

Ensure full documentation of meeting discussions, decisions and action items.

Track & ensure completion of agreed action items.

Ensure appropriate archiving of project documentation.

Develop a monthly report that provides an overview of progress on all key activities, potential risks and mitigation actions.

Generate and maintain strategic integrated GOMA Franchise project plans, project timelines, high quality risk management plans, and communication plans, as needed.

Responsibilities Continued Operational Excellence Support Collaborate with Executive Director, Strategy & Operational Excellence to further strengthen operational excellence from a GOMA-wide organization perspective.

Disseminate key leadership communications throughout GMAT/Functional teams and lead issue escalation efforts when required.

Identify gaps in Global Oncology Medical Affairs processes and functional procedures that (potentially) impact program delivery and escalate appropriately to Executive Director, Strategy & Operational Excellence.

Collaborate with Executive Director, Strategy & Operational Excellence and GMAT/Functional Leads for formal presentations/communications to GOMA Head and GOMA Leadership Team.

Support Executive Director, Strategy & Operational Excellence with updates to GOMA leadership, as needed.

Integrate operational excellence best practices into regular team meetings and communications to enhance overall capabilities.

Qualifications Education Qualifications Bachelor's Degree with relevant professional experience or equivalent required advanced degree preferred Experience Qualifications 7 or More Years experience in project management with at least five years in pharmaceutical industry.

required Medical Affairs experience strongly preferred preferred Demonstrated leadership skills, especially in the areas of communication and change management required Meticulous attention to detail in all aspects of work and expert organization skills required Proven ability to drive decision making process, including ability to challenge teams and achieve excellence required Ability to thrive in a fast-paced environment required Self-starter, results-oriented required Strong change management skills and engagement to enable continuous improvement required Strong communication skills and ability to adapt according to different levels of management required Ability to negotiate and align across teams required Demonstrated ability to collaborate effectively with key stakeholders required Strong Microsoft Office skills required required Travel Requirements Must be able to travel domestic and international 10% Additional Information Daiichi Sankyo, Inc.

is an equal opportunity/affirmative action employer.

Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Salary Range: USD$198,160.00
- USD$297,240.00 Download Our Benefits Summary PDF
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Air Interdiction Agent
$41 - 53.29
Belle Mead, NJ 2 days ago

PilotCBP Air Interdiction Agent

NEW RECRUITMENT AND RETENTION INCENTIVES!

Air and Marine Operations (AMO), a component of U.S. Customs and Border Protection (CBP), offers skilled Pilots interested in law enforcement an opportunity to work with an elite team of highly trained professionals whose camaraderie, pride, and purpose are hallmarks of their daily mission to protect America.

If you are looking for an exciting and rewarding career with excellent pay, exceptional federal benefits and job stability, now is the time to make your move: become an Air Interdiction Agent. AMO is actively recruiting for these full-time security-based opportunities with a streamlined application process. Notably, seasoned pilots and those with military training are in demandAPPLY TODAY!

DONT FORGET TO CHECK OUT THE INCENTIVES SEE SALARY SECTION BELOW!

Duty Locations

Locations are offered based on operational requirements, mission requirements, and critical agency hiring needs as determined by AMO. You must be willing to work at any duty location within the region you select to include but not limited to the following:

Southeast Region:Homestead, FL and CAMB:Aguadilla, PR

Southwest Region: Tucson and Yuma, AZ; San Diego, CA; El Paso, Laredo, and McAllen, TX

NASOC UAS locations:Sierra Vista, AZ; San Angelo, TX

Duties and Responsibilities

As an Air Interdiction Agent (AIA) you will perform aviation-based law enforcement operations for the detection, prevention, interdiction, and apprehension of terrorists, terrorist weapons, and other contraband and persons from illegally entering or attacking the United States. Typical duties include:

  • Conducting air patrol, surveillance, and pursuit activities related to the interdiction of smuggled contraband via land vehicles, aircraft, or vessels.
  • Monitoring behavior patterns and activities of suspect persons, vehicles, or vessels believed to be engaged in illegal activities.
  • Collecting, refining, and analyzing strategic and tactical intelligence.
  • Supporting search and rescue and humanitarian efforts.

Salary and Benefits

Begin your career as an Air Interdiction Agent (AIA) and make up to $85,270 to - $110,846 per year based on your qualifications for the GS-11 grade level and possible extra compensation based on your duty location (see below).

Recruitment Incentive:New hires may be eligible to receive a one-time Recruitment Incentive payout of $10,000 after completing Federal Law Enforcement Training Academy (FLETC) (1 year service agreement will need to be completed) (Recruitment Incentive is only available to new Federal employees as described in 5 CFR 575.102. Eligibility will be determined by Human Resources.)

Your starting salary will include Special Salary Rate (SSR); Law Enforcement Availability Pay (LEAP); Recruitment Incentive; and Retention Incentive.

This career ladder position has a grade level progression of GS-11, GS-12, and GS-13. You may be eligible for a promotion to the next higher grade level automatically (without re-applying) once you complete 52 weeks at each grade level (with supervisor approval).

Example of annual compensation for the first three years at our new-hire locations which are currently authorized to receive LEAP (amounts below include the SSR + LEAP).

  • GS-11, 1st year annual pay - $106,588
  • GS-12, 2nd year annual pay - $127,754
  • GS-13, 3rd year annual pay - $151,918

Example of annual compensation for the first three years at our new-hire locations which are currently authorized to receive a 10% Retention Incentive (amounts below include the SSR + LEAP + 10% Retention Incentive UAS Sites: Sierra Vista, AZ; Grand Forks, ND; San Angelo, TX).

  • GS-11, 1st year annual pay - $115,115
  • GS-12, 2nd year annual pay - $137,974
  • GS-13, 3rd year annual pay - $164,071

Example of annual compensation for the first three years at our new-hire locations which are currently authorized to receive a 25% Recruitment Incentive (amounts below include the SSR + LEAP + 25% Recruitment Incentive CAMB location only; Aguadilla, PR).

  • GS-11, 1st year annual pay - $127,906
  • GS-12, 2nd year annual pay - $153,305
  • GS-13, 3rd year annual pay - $182,302

Retention Incentive: Retention Incentive is contingent on eligibility. Eligibility will be determined by Human Resources.

  • RI: Retention Incentive (25% for UAS Sites, Sierra Vista, AZ, Grand Forks, ND, San Angelo, TX)
  • RI: Retention Incentive (25% for Key West, FL)

RI: Retention Incentive (25% for Caribbean Air and Marine Branch (CAMB) and subordinate locations)

Air Interdiction Agents are eligible to select from an array of federal employment benefits that include health, dental and other insurance plans, a generous annual and sick leave program, and participation in the Thrift Savings Plan, a retirement plan akin to a traditional and ROTH 401(k) offering.

Qualifications

Experience:You qualify for the GS-11 grade level if you possess one (1) year of specialized professional aviation experience performing duties such as:

  • Flying as a Pilot-in-Command or sole manipulator in an airplane and helicopter in all environments of flight, including night, poor weather, unfavorable terrain, low altitudes, or speed.
  • Evaluating information rapidly and making judicious decisions promptly during in-flight operations.
  • Developing strategies and coordinating aircraft and ground assets.
  • Using information systems and databases to conduct information surveys, queries, update files and disseminate information.
  • Experience may include Operation of an aircraft as Captain, Pilot in Command, Aircraft Commander, First Officer, Certified Flight Instructor, Second in Command, or Co-pilot.

Hiring Minimums:

Certification & Ratings: A current FAA Commercial or ATP Pilot Certification with one of the following ratings:

  • Dual Rated: Airplane (Single-engine land or multi-engine land) with instrument rating AND Rotorcraft Helicopter with instrument rating.
  • Airplane Rated: Airplane (Single-engine land or multi-engine land) with instrument.
  • Helicopter Rated: Rotorcraft Helicopter with instrument rating.
  • Equivalent military rating of the above at the time of application (eligibility based on military flight experience must provide official orders, forms or logbooks showing their status as a rated military pilot).

Flight Hours: Pilot Enter on Duty minimums are 1500 flight hours; (up to 500 hours can be waived, reducing the pilot enter on duty minimums to 1000 hours.

250 Pilot-in-Command hours; 75 Instrument hours; 75 Night hours (Flight Hour Waiver available, see Required Documents); and 100 Flight hours in the last 12 months This qualification requirement is currently being waived by OPM through August 5, 2025.

FAA Class 2 medical required for assessment dated within the last 12 calendar months; FAA Class 1, FAA Class 2 or Military medical flight clearance dated within the last 12 months qualifies to start the pre-employment process for the AIA position.

Apply at 750 hours total time: Applicants applying at 750 flight hours are required to obtain at least 1,000 flight hours (depending on the number of hours approved for a waiver) at their own expense before being able to attend the 3-part flight assessment. Applicants must still meet 250 Pilot-in-Command, 75 instrument, and 75-night hours (100 flight hours in the last 12 months. This qualification requirement is currently being waived by OPM through August 4, 2026)

UAS Flight Hours:Applicants may include UAS Predator A (MQ-1), Predator B (MQ-9) flight hours and Predator A (MQ-1), Predator B (MQ-9) or predator-based flight hours. These hours may be credited towards satisfying the ""Total flight time"" 1,500 flight hour requirement only. UAS hours do not count towards the 250 flight hours as a Pilot in Command, 75 flight hours Instrument, and 75 flight hours Night. Flight hour logbooks will be required at the time of your Flight Assessment for verification.

Other Requirements

Citizenship: You must be a U.S. Citizen to apply for this position.

Residency: You must have had primary U.S. residency (includes protectorates as declared under international law) for at least three of the last five years.

Age Requirement: Provisions of Public Laws 93-350 and 100-238 allow the imposition of a maximum age for initial appointment to a primary Law Enforcement Officer position within the Department of Homeland Security (DHS). In accordance with DHS Management Directive 251-03, the ""day before an individual's 37th birthday"" is the maximum age for original appointment to a position as a primary law enforcement officer within DHS. The age requirement is also necessary to ensure that you are able to complete the 20 years of applicable service for retirement.

NOTE: The Commissioner of CBP has approved a temporary increase in the maximum allowable age to 40 for original placement into an Air Interdiction Agent position.

Age Waiver: Creditable law enforcement officer service -Covered by Title 5 U.S.C. 8336(c) or Title 5 U.S.C. 8412(d), or creditable service covered by Title 5 U.S.C. 8401(36) (as a Customs and Border Protection Officer) on or after July 6, 2008, may be applied toward the maximum age requirement. This age restriction may not apply if you are currently serving in a federal civilian (not military) law enforcement position covered by Title 5 U.S.C. 8336(c) or Title 5 U.S.C. 8412(d).

Veterans' Preference Eligibility: To ensure compliance with statutes pertaining to the appointment of preference eligible veterans as determined by the Merit Systems Protection Board in its decisionIsabellav.Dept of State,the maximum age for original appointment articulated above shall not apply to the hiring of individuals entitled to veterans' preference eligibility under 5 U.S.C. 3312. You must submit proof of Veteran's Preference (DD-214 Member 4 Copy) at the time of application.

Training:This position has a training requirement. You may be required to successfully complete the training requirement as a condition of employment. Failure to successfully complete the required course(s) of training in accordance with CBP standards and policies will result in placement into either a former or different position, demotion, or separation as determined by management and appropriate procedures.

Travel Required: You may be expected to travel for this position based on operational needs.

How to Apply

There Are Three Ways to Apply to Become an Air Interdiction Agent:

  • Fill out theAir Interdiction Agent applicant checklistand email it to a recruiter at along with a copy of your resume; OR
  • Apply onUSAJOBS;OR
  • Apply onAirline Apps.

Stay Updated Opt into CBPs talent repository (highly recommended) by selecting the Contact a Recruiter button. For Position of Interest select Air and Marine Operations, Air Interdiction Agent, then complete the pre-screening questions. Youll receive monthly emails with information about webinars, career expos, and future opportunities with AMO and CBP.

RequiredPreferredJob Industries
  • Government & Military
permanent
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