Jobs in Hamilton Township, NJ
391 positions found — Page 4
CDL A Benefits A clear path to ownership 70% of line haul 100% fuel surcharge No money down, walk-away lease Freightliner Cascadia trucks in various colors Truck payment options to meet any budget from $695/week to $1,095/week Rider & Pet Policy Access to Health, Dental, Vision, and Life Insurance at Group Rates Weekly Settlement CDL A Job Requirements Class A CDL 1 Year verifiable driving experience Reefer experience preferred 23 Years or older Acceptable Driving Record Available Equipment Newer Model Equipment Brush guards APUs in each truck Wi-Fi equipped Extended Warranty Program About Us At R.E.
Garrison Trucking, Inc., we appreciate our drivers—they are an integral part of our team.
Just like our drivers are committed to helping others every day, we are committed to taking care of our drivers, day in and day out.6b250ea6-cee3-481d-915c-f7283f1b2f1b
Job Title: RedHat OpenShift & Kubernetes SME
Location: Princeton - NJ - 08540
Mode : Contract (6+ Months) – Onsite
Min 15 Years of experience required.
Qualifications:
Design, deploy and maintain Red Hat OpenShift and Rancher Managed Kubernetes Clusters
Architect Highly available, scalable, and secure container platforms
Install, configure, upgrade and patch OpenShift and Rancher Clusters
Implement logging, monitoring, and alerting (Prometheus, Grafana, EFK etc.)
Troubleshoot Cluster, Networking, Storage, and application issues
Perform root cause analysis and provide performance optimization
Act as an SME for OpenShift and Rancher Technologies
Provide guidance to Customer and application teams
Create documentation, standards, and operational runbooks
Strong Hands-on experience with RedHat Open Shift and Rancher (RKE, RKE2)
Expert knowledge of Kubernetes architecture and Operations
Experience supporting mixed OS environments (Windows and Linux).
Excellent communication skills, able to explain complex concepts to technical and non-technical audiences.
Demonstrated ability to work independently and as part of a team.
Relevant certifications (RHCA, CKA, CKAD, etc.) and active participation in the Kubernetes community are a plus.
Experience with CI/CD Pipelines
Title: Early Career Recruiter
On-site – East Windsor, NJ
We are looking for recent graduates or early-career professionals who are interested in starting a career in Technical Recruiting / Talent Acquisition. This role offers hands-on training, mentorship, and growth into a full-cycle recruiter role.
What You'll Learn & Do:
Learn how to recruit for software, IT, and engineering roles
Work closely with senior recruiters and hiring managers
Source candidates using LinkedIn, job boards, and internal databases
Screen resumes and conduct initial candidate interviews
Coordinate interview schedules and follow-ups
Support onboarding and offer processes
Build candidate pipelines and maintain recruiting data
Represent the company at career fairs and campus events
Ideal Candidate:
Recent graduate or up to 1–2 years of experience
Bachelor's degree in HR, Business, Marketing, Psychology, or related field
Strong communication and interpersonal skills
Interest in recruiting, HR, or talent acquisition
Organized, eager to learn, and comfortable talking to people
Basic computer skills (MS Excel, Word, LinkedIn)
What We Offer:
Structured training & mentorship
Clear growth path to Technical Recruiter / Senior Recruiter
Exposure to US staffing & IT hiring
Visa sponsorship available
Overview
The position will be responsible for day-to-day accounting activities for operations to help ensure that the books are closed on time, in accordance with GAAP, and without material misstatement.
Responsibilities:
- Responsible for accounting, reporting, and analysis.
- Complete monthly accounting close, including journal entry preparation and balance sheet reconciliations.
- Work closely with the plants, legal, asset management, etc., to understand various operational issues and related accounting implications.
- Coordinating payments with Treasury and accounts payable team members.
- Experience in a fast-paced environment, including the ability and experience to meet firm deadlines, including monthly close on a defined schedule.
- Assist with special projects as requested.
- Hybrid schedule, e.g., 4 days in the office, and the balance of the week is remote
Requirements:
- Bachelor's degree in accounting, business, or finance.
- Knowledge of general ledger and reporting software
- Proficient with Microsoft Office applications, particularly Excel, with knowledge of advanced features such as pivot tables and lookups.
- Experience in general financial accounting and reporting.
- Demonstrated ability to communicate with all levels of internal and external contacts
- Ability to work independently in a team-oriented culture in a fast-paced environment.
- Experience with SAP preferred.
- Pursuing or holds CPA, preferred.
- Prior experience in the energy industry or a similar commodity-based business is preferred.
- Proven analytical and problem-solving skills; demonstrated planning and organizing skills; ability to think strategically/long-term.
- Proficient with Microsoft Office applications.
- Attention to detail
- Strong time management skills applications
Hi,
I am Suresh Durgam from iPivot. Please find the job description below for your reference. If interested, reply with an updated resume at
Job Title: Node.js Developer
Location: Princeton, NJ (2 Days onsite a week)
Duration: W2 Contract
Note: Only U.S. citizens (NJ/NY/PA) are required.
Skills & Experience Requirements
Strong proficiency in Node.js and TypeScript
Knowledge of Nest.js is a big plus
Proven experience building AWS Lambda based microservices
Solid working knowledge of core AWS services, including:
API Gateway
DynamoDB (NoSQL)
RDS / Aurora PostgreSQL (SQL)
S3, SNS, SQS
CloudWatch (logs, metrics)
Experience designing and developing serverless REST APIs
Familiarity with Infrastructure-as-Code (AWS CDK or Cloud Formation)
Good understanding of SQL and NoSQL data modeling
Experience with distributed systems, event-driven architectures, and asynchronous processing
Ability to build secure, scalable, and maintainable cloud applications
Familiarity with DevOps workflows, CI/CD pipelines (GitLab or GitHub Actions), and unit/integration testing
Knowledge of best practices for logging, validation, error handling, and API performance in AWS
Experience in FedRAMP or other high-compliance environments is a plus
Good communication and collaboration skills in Agile/Scrum or SAFe environments.
Suresh Durgam
E:
/in/suresh-durgam
Remote working/work at home options are available for this role.
At Airgas, we are committed to building a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world.
Airgas is Hiring for a Field Sourcing Specialist
- This position is a hybrid role and can be located near any of our DCs in: Levittown, PA, Germantown, WI, Coppell, TX, Henderson, NV, Springdale, OH
- Base Pay: $70,000 to $74,000 annual
- Travel is 10%.
Quentin Chavis Jr. / / 346-459-4397
Job Description Summary: Provide dedicated professional sourcing and other value creation services to assigned business units or operating zones to support and achieve safety, efficiency, compliance and savings initiatives and objectives. Specific activities include competitive bidding, proposal analysis, negotiation of price and commercial terms, vendor management and asset sales
- Lead bidding and sourcing activities for all purchases by assigned zone or business unit (BU): o Manage all contact between Airgas and bidders.
- Assist in developing technical specifications and/or scopes of work with internal customers. o Investigate, qualify and recommend bidders.
- Develop and issue formal requests for quotes (RFQ's).
- Lead job walks and bid clarification meetings with internal customers.
- Issue clarifications or amendments to the specification or work scope to all bidders.
- Complete commercial bid tabulations.
- Complete technical bid tabulations including analysis with internal customers.
- Negotiate final price and commercial terms.
- Make sourcing recommendations to internal customers.
- Author and execute materials and services contracts as required.
- Manage commercial risk for all purchases by assigned zone or business unit:
- Identify and address business risks during the bidding and sourcing process.
- Verify that all contractors are appropriately pre-screened for safety, and initiate the contractor pre-screening process for new contractors as required.
- Verify that hold harmless and indemnification documentation is in place as well as a current certificate of insurance is on file with all contractors. Initiate and negotiate hold harmless and indemnification documentation for new contractors as required.
- Verify that critical suppliers are on the approved supplier list, and initiate the critical supplier qualification process for new suppliers as required.
- Proactively manage sourcing activity for all major capital, maintenance and plant turnarounds (TAR): o Attend and actively participate in budget planning meetings for assigned BU or zone.
- Actively participate in TAR planning meetings.
________________________
Are you a MATCH?
Required Qualifications:
- High School diploma required
- At least five years purchasing experience supporting operations or manufacturing
- Previous experience implementing cost savings programs/initiatives
Preferred Qualifications:
- Bachelor's Degree from an accredited institution
- Previous SAP experience preferred
- Previous chemical manufacturing experience a plus
________________________
Benefits
We care about and support our Airgas Families. This is evident not only through our competitive compensation but also through a comprehensive benefits package that includes medical, dental, and vision plans, short-term and long-term disability, life and accidental death and dismemberment (AD&D) insurance, Employee Assistance Program (EAP), pre-tax commuter transportation benefit, parental leave, vacation, sick time, floating holidays, jury duty and funeral/bereavement leave, and paid holidays for all eligible full-time employees.
Additionally, we offer our eligible employees a 401k plan with company matching funds, tuition reimbursement, discounted college tuition for eligible employees' dependents, and an Airgas Scholarship Program for dependent children.
Associates who are members of collective bargaining units should review their bargaining agreement to determine whether they are eligible for some or all of the benefits described here and to see any special terms or conditions for eligibility.
_________________________
Your DIFFERENCES enhance our PERFORMANCE
At Airgas, we are committed to building a workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world.
We welcome and consider applications from all qualified applicants, regardless of their race, gender, sexual orientation, religion, disability or any other protected characteristic. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world.
_________________________
About Airgas
Airgas, an Air Liquide company, is a leading U.S. supplier of industrial, medical and specialty gases, as well as hardgoods and related products; one of the largest U.S. suppliers of safety products; and a leading U.S. supplier of ammonia products and process chemicals. Through the passion and diversity of its 18,000 associates, Airgas fosters a culture of safety, customer success, sustainability and innovation. Airgas associates are empowered to share ideas, take initiative and make decisions.
Airgas is a subsidiary of Air Liquide, a world leader in gases, technologies and services for industry and healthcare. Present in 60 countries with approximately 66,500 employees, Air Liquide serves more than 4 million customers and patients.
Join us for a stimulating experience: At Airgas, you matter and so does the work you do. As a member of our team, you play an important role in the success of your team, making sure our products are created sustainably and delivered safely and efficiently. In turn, you'll find a welcoming workplace where you're valued for who you are and where you can fill your potential while growing a fulfilling career — whatever path you choose.
_________________________
Equal Employment Opportunity Information
We are an equal opportunity employer. We welcome all qualified applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic.
Airgas, an Air Liquide Company is a Government contractor subject to the Vietnam Era Veterans' Readjustment Assistance Act of 1974 and Section 503 of the Rehabilitation Act of 1973.
Airgas does not discriminate against qualified applicants with disabilities, and is committed to providing reasonable accommodations to the known disabilities of such individuals so as to ensure equal access to benefits and privileges of employment. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact us by email at .
_________________________
California Privacy Notice
Java Developer
Must have Java + Spring Boot
DESCRIPTION:
Job Responsibilities:
● Develop applications using Java 8/JEE (and higher), Angular 2+, React.js, SQL, Spring, HTML5, CSS, JavaScript and TypeScript among other tools.
● Write scalable, secure, maintainable code that powers our clients' platforms. ● Create, deploy and maintain automated system tests.
● Works with Testers to understand defects opened and resolves them in a timely manner ● Support continuous improvement by investigating alternatives and technologies and presenting these for architectural review
● Collaborates effectively with other team members to accomplish shared user story and sprint goals
Requirement:
● Experience in a programming language Java and JavaScript
● Decent understanding of the software development life cycle
● Basic programming skills using object-oriented programming (OOP) languages with in-depth knowledge of common APIs and data structures like Collections, Maps, lists, Sets etc.
● Knowledge of relational databases (e.g. SQL Server, Oracle) basic SQL query language skills
Preferred Qualifications:
● Master's Degree in Computer Science (CS)
● 0-1 year of practical experience in Java coding
● Experience using Spring, Maven and Angular frameworks, HTML, CSS ● Knowledge with other contemporary Java technologies (e.g. Weblogic, RabbitMQ, Tomcat, etc.) · Knowledge of JSP, J2EE, and JDBC
About Made Scientific
Made Scientific is a leading US-based cell therapy contract development and manufacturing organization (CDMO) specializing in the development, manufacturing, and release of autologous and allogeneic cell therapy products for clinical-and-commercial supply. Operating from two U.S.-based manufacturing facilities, Made Scientific combines the agility and entrepreneurial spirit of a specialist CDMO with the global expertise and resources of GC Corporation of South Korea, a global leader in the pharmaceutical and biotechnology sectors.
Position Summary
The Director of Manufacturing Science & Technology (MSAT) will lead the technical oversight, process lifecycle management, and technology transfer activities for cell therapy manufacturing programs within a CDMO environment. This role is responsible for ensuring robust, scalable, and compliant manufacturing processes for autologous and allogeneic cell therapy products from clinical development through commercial manufacturing.
The Director will work cross-functionally with Process Development, Manufacturing, Quality, Regulatory, Supply Chain, and Client Program teams to support client programs, drive continuous process improvement, and ensure successful technology transfers into GMP manufacturing.
This role is based in Princeton, NJ and is fully onsite.
Key Responsibilities
• Provide scientific and technical leadership for cell therapy manufacturing processes, including upstream cell expansion, gene modification, harvest, formulation, and cryopreservation.
• Serve as the technical subject matter expert (SME) for manufacturing processes supporting client programs.
• Lead troubleshooting efforts and root cause analysis for manufacturing deviations, investigations, and CAPAs.
• Drive implementation of process monitoring and control strategies.
• Lead technology transfer activities from clients or internal process development teams into GMP manufacturing.
• Develop and review technology transfer plans, process descriptions, risk assessments, and gap analyses.
• Ensure successful scale-up and scale-out of manufacturing processes across CDMO facilities, as applicable.
• Oversee continued process verification (CPV) and lifecycle management for manufacturing processes.
• Lead process characterization, comparability studies, and validation support activities.
• Provide real-time technical support to GMP manufacturing operations for clinical and commercial batches.
• Review batch records, deviations, and change controls related to process changes.
• Present technical updates during client meetings and governance reviews.
• Support proposal development, technical due diligence, and onboarding of new client programs.
• Ensure MSAT activities comply with cGMP, FDA, EMA, and ICH regulatory requirements.
• Contribute to regulatory filings, including INDs, BLAs, and comparability packages.
• Support regulatory inspections and client audits.
• Build and lead a high-performing MSAT team, including scientists and engineers.
• Provide mentorship, technical guidance, and performance management.
• Develop MSAT strategy aligned with organizational growth and client pipeline.
• Perform other duties as assigned by the Head of Development.
Required Qualifications
• PhD or MS in Biochemical Engineering, Cell Biology, Bioengineering, Biotechnology, or a related field.
• 10–15+ years of experience in biopharmaceutical manufacturing or process development.
• 5+ years of leadership experience in MSAT, technical operations, or process development.
• Strong experience in cell therapy manufacturing (e.g., CAR-T, TCR-T, NK cells, stem cell therapies).
• Experience working within a CDMO environment strongly preferred.
• Deep knowledge of:
• Cell culture and expansion technologies
• Viral vector transduction or gene editing workflows
• Closed and automated cell therapy manufacturing platforms
• Cryopreservation and fill-finish processes
• Experience with technology transfer, process validation, and process characterization.
• Familiarity with statistical process monitoring and data analytics tools.
• Strong cross-functional leadership and project management skills.
• Experience working directly with biotech clients.
• Excellent written and verbal communication skills.
• Ability to operate in a fast-paced CDMO environment supporting multiple client programs.
Preferred Qualifications
• Experience with commercial cell therapy manufacturing.
• Experience with automated manufacturing platforms (e.g., CliniMACS Prodigy, Lonza Cocoon).
• Knowledge of viral vector manufacturing processes.
• Experience supporting BLA submissions or late-stage clinical programs.
Physical Requirements
• Ability to perform essential job functions in compliance with ADA, FMLA, and other applicable regulations, including meeting productivity standards.
• Ability to maintain regular and punctual attendance.
• Must be willing to become gown-qualified and work in BSL-2 lab, CNC, ISO7, and ISO8 environments.
• Ability to lift and carry up to 30 lbs.
• Ability to bend, stoop, reach, climb, and stand on elevated surfaces as needed.
• Ability to sit or stand for extended periods.
• Must be comfortable working with cell-based products, chemicals, or hazardous materials.
About Cygnus Professionals, Inc.
Cygnus is a Princeton, NJ-headquartered global Business IT consulting and software Services firm with offices in the USA and Asia. Cygnus offers and enables innovation and helps our clients accelerate time to market & grow their business. Over 15 years, we have taken great pride in continuing our deep relationships with our clients.
For further information about CYGNUS, please visit our website Title: Data Architect
Location: Princeton, New Jersey – Onsite
W2 Contract
Job Summary
We are seeking an experienced Data Architect to design, build, and maintain scalable data architecture solutions supporting enterprise analytics, data integration, and digital transformation initiatives. The ideal candidate will work closely with business stakeholders, data engineers, and application teams to design robust data models, data pipelines, and enterprise data platforms that support advanced analytics and reporting.
Key Responsibilities
- Design and implement enterprise data architecture frameworks and best practices.
- Develop logical and physical data models for enterprise data platforms.
- Architect data lakes, data warehouses, and data integration solutions across cloud and on-prem environments.
- Collaborate with data engineers and application teams to build scalable data pipelines and ETL/ELT processes.
- Ensure data governance, data quality, security, and compliance standards are implemented across the data ecosystem.
- Evaluate and recommend data technologies, tools, and frameworks aligned with enterprise strategy.
- Provide architectural guidance for cloud-based data platforms (AWS/Azure/GCP).
- Optimize performance for large-scale data processing and analytics workloads.
- Support business intelligence, reporting, and advanced analytics initiatives.
Required Qualifications
- 10+ years of experience in data architecture, data engineering, or enterprise data management.
- Strong experience with data modeling (conceptual, logical, physical).
- Expertise with data warehouse and data lake architectures.
- Hands-on experience with ETL/ELT tools and data integration platforms.
- Experience with SQL and large-scale data platforms (Snowflake, Redshift, BigQuery, etc.).
- Experience working with cloud data platforms (AWS, Azure, or GCP).
- Strong understanding of data governance, data quality, and metadata management.
- Experience with big data technologies (Spark, Hadoop, Kafka) is a plus.
Preferred Skills
- Experience in Healthcare, Pharmaceutical, or Life Sciences domain.
- Knowledge of Master Data Management (MDM) and data catalog tools.
- Familiarity with BI tools such as Tableau, Power BI, or Looker.
- Strong communication skills to interact with business and technical teams.
Education
- Bachelor’s or Master’s degree in Computer Science, Information Systems, Data Science, or related field.
Cygnus Belief
We believe in our commitment to diversity & inclusion.
Equal Employment Opportunity Statement
Cygnus is an Equal Opportunity Employer. We ensure that no one should be discriminated against because of their differences, such as age, disability, ethnicity, gender, gender identity and expression, religion, or sexual orientation.
All our employment decisions are taken without looking into age, race, creed, color, religion, sex, nationality, disability status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status, or any other aspects of employment protected by federal, state, or local law. Applicants for employment in the US must have work authorization.
Job Description for Project Management Associate - Fulltime and Onsite.
Project Management Associate is accountable for working projects by organizing meetings and coordinating follow-ups with internal and external project stakeholders across the globe. The projects would include R&D, site transfers, technology transfers, site transfers, and any source variation. Coordinate shipment of innovator samples. Perform business analysis and create term sheets as required. This individual will report into Sr. Director, Corporate Development.
Responsibilities:
Projects:
· Drive 3rd party projects to completion
· Support the India team for approvals and documentation required from Bion team
· Organize meetings, publish meeting notes/action items, and follow-up on action items.
· Understand and manage project schedules, and critical path activities
· Follow up with vendors, and internal team on deliverables.
· Update the project tracker on weekly basis.
· Identify and inform the project issues to the project team and stakeholders, and work with the team to resolve issues
· Conduct lessons learned sessions upon project completion.
RLD Shipments:
· Identify RLD requirements, and create proforma invoices
· Coordinate RLD sourcing and shipments
· Track RLD shipments through delivery
Smartsheet:
· Implement Smartsheet across all locations
· Manage Smartsheet to generate weekly and monthly reports to track project progress
· Identify areas to expand Smartsheet implementation
API Vendors:
· Coordinate with Logistics/Vendors to ship and track project related shipments such as API, samples etc for key product launches
New Business Opportunities:
· Create market share reports
· Follow up on all licensing opportunities
· Create and generate reports weekly, monthly, and ad-hoc.
· Proficient in Microsoft Office Excel and Powe point applications
. Ability to build business case
Compliance:
· Stay compliant with Site training requirements in SOPs and cGMPs
Qualifications:
· Bachelor’s degree required, preferably in Engineering, Supply Chain or Operations
· 2 to 3 years of prior generics pharmaceutical project management and analysis experience
· Ability to work with cross-functional teams and multiple site teams
· Ability to work with collaborative project management tools
· Preferred experience in Microsoft Office applications including Visio, MS Project
Additional Qualifications:
· Problem solver, Go-getter, and ability to collaborate
· Ability to act in an ethical, honest and professional manner at all times
· Ability to speak and write English in a clear and understandable manner
· Must have the ability to carry out instructions furnished in both oral and written form
Job Location: BionPharma, Inc. Princeton, New Jersey.