Engineering Jobs in Kendall Park Middlesex

H

Site Quality Manager

✦ New

Salary not disclosed

Piscataway, NJ 16 hours ago

Overview

The Site Quality Manager is responsible for leading the quality function at their site and developing, implementing, and continuously improving the Humanscale Business System which exceeds customer expectations, satisfies regulatory requirements, improves operational efficiency, and reduces the cost of poor quality.

Essential Functions

Customer Focus and Continuous Improvement
Promote a quality culture and customer focused approach
Capture the Voice of the Customer through customer feedback to enable development and value chain to improve design and execution
Drive timely and effective resolution of customer issues
Leadership
Lead the Quality Assurance, Quality Control, and Quality Testing functions within the site
Supervise workers engaged in the inspection and testing of activities to ensure efficient productivity and high technical integrity
Manage the performance of the team through key performance metrics. Develop team to continuously improve performance and results
Design, develop, and implement quality control training programs
Conduct or arrange periodic training sessions to keep team members informed on proper procedures and methods
Operations
Establish and deploy site Quality objectives in line with Global Quality objectives
Analyze and communicate the adequacy and effectiveness of the Humanscale Business System through performance metrics
Coordinate and participate in Material Review Board (MRB) meetings
Lead and participate in root cause analysis
Drive effective corrective actions to prevent recurrence of non-conformances utilizing A3/SPS, 8D, and similar tools
Execute cost of poor quality reduction measures to drive company savings
Ensure compliance with customer, industry, and regulatory requirements
Improve and error-proof business processes utilizing SS / Lean methodologies
Develop, implement, and maintain quality specifications and standards for all raw materials, components, and finished goods
Create, document, and implement inspection criteria and procedures
Quality System
Lead site Quality Performance Reviews
Lead internal audits and drive timely closure of findings
Apply total quality management tools and approaches to analytical and reporting processes

Qualification

Bachelor’s degree from an Engineering discipline (Mechanical preferred)
Minimum of 3-5 years of experience in Quality Control in a manufacturing environment
Minimum of 2 years of management experience
Knowledge of Quality Management Systems, especially ISO 9000
Knowledge of ERP systems, especially Oracle and Infor, is highly desirable
Lean Manufacturing experience a plus
Experience with developing/documenting procedures
Excellent interpersonal skills to lead the quality function to a higher level of performance
Demonstrated customer focus, with drive and determination to improve quality performance
Able to direct and lead others to produce desired results
Demonstrated analytical skills, combining multiple data sources to create quality insights that drive improvement.
Demonstrates attention to detail and thrives in a team environment.
Exercise initiative, achievement, and independent judgment

WHAT WE OFFER:

Competitive base
Medical Benefits (Medical, Dental, Vision)
HSA, FSA, Commuter Benefits
Medical Discounts
Ancillary Benefits
Accident, Critical Illness, Hospital Insurance
Voluntary, Spouse, and Child Life Insurance
Pet Insurance
Employee Discount Programs
401k matching
Paid time off (including 15 PTO days and 11 holidays)

Salary Range: $86,829 - $126, 649

Please note that the salary information is a general guideline. Humanscale considers other factors such as (but not limited to) scope and responsibilities of the position, candidate’s work experience, education/training, key skills, internal peer equity, as well as market location and business considerations when extending an offer.

Company Overview

Humanscale is the premier designer and manufacturer of ergonomic products that improve health and comfort at work. We have a focus on sustainability with 70% of our products currently certified as having a Net Positive impact on the environment. Our award-winning office products – seating, sit/stand desks, technology support and lighting – have led the industry in performance and simplicity for over 40 years.

Humanscale is an Equal Opportunity Employer (Disabled/Veteran)

Scam Notice: Please be aware that there are individuals and organizations that may attempt to scam job seekers by offering fraudulent employment opportunities in the name of Humanscale. These scams may involve fake job postings, unsolicited emails, or messages claiming to be from our recruiters or hiring managers. Humanscale will never ask for any personal account information, such credit card details or bank account numbers, during the recruitment process.

Not Specified

Formulation Scientist

✦ New

🏢 Medasource

Salary not disclosed

Skillman, NJ 5 hours ago

Position: Formulation Scientist

Location: Onsite in Skillman, NJ

Duration: 1 year Contract

Overview

The Formulation Scientist will support the Skin Health R&D team, contributing to both innovation and base business (commercialized products) within the skincare portfolio. This role will focus on formulation development, lab execution, and scale-up activities for consumer skincare products, including anti-aging formulations.

The ideal candidate will work under the guidance of senior scientists while also taking ownership of experiments, technical problem-solving, and project execution.

Key Responsibilities

Support end-to-end product development for skincare formulations, including innovation and commercialization of existing products
Execute laboratory experiments, including formulation development, testing, and analysis of skincare products
Assist in product design, formulation optimization, and process development/scale-up activities
Conduct Design of Experiments (DOE) to support investigations and product improvements
Process formulated products at lab scale and support transition to manufacturing
Collaborate cross-functionally with R&D, manufacturing, and external partners to support project execution
Analyze consumer insights and contribute to innovation pipeline development
Maintain accurate documentation, including technical reports and experimental data
Ensure compliance with company procedures, cGMP standards, and regulatory requirements
Support troubleshooting efforts related to formulation, supply disruptions, or product upgrades

Required Qualifications

Bachelor’s degree in Chemistry, Chemical Engineering, Pharmacy, or related field
1–4 years of experience in formulation development (academic or industry)
Experience with personal care, cosmetic, OTC, or pharmaceutical products
Strong foundation in formulated systems (emulsions, surfactants, suspensions, structured liquids)
Hands-on laboratory experience executing experiments and processing formulations
Understanding of material chemistry and basic process equipment
Experience supporting process development or scale-up activities
Strong communication, documentation, and organizational skills
Proficiency in MS Office (Excel, Word, PowerPoint)

Preferred Qualifications

Experience formulating skincare or anti-aging products
Familiarity with cGMP and regulatory standards
Experience working with external manufacturing partners
Exposure to technical project management or cross-functional collaboration
Ability to work independently while contributing within a team environment

Not Specified

M

Director, MSAT

✦ New

🏢 Made Scientific

Salary not disclosed

Princeton, NJ 16 hours ago

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.

Not Specified

C

Senior Data Architect

✦ New

🏢 Cygnus Professionals Inc.

Salary not disclosed

Princeton, NJ 16 hours ago

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.

Not Specified

P

Project Management Associate

✦ New

Salary not disclosed

Princeton, NJ 16 hours ago

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.

Not Specified

Principal Security Engineer - Remote flexibility across the US (Remote)

✦ New

🏢 GoDaddy

Salary not disclosed

Remote, Oregon 16 hours ago

Location Details: United States - Remote

At GoDaddy the future of work looks different for each team. Some teams work in the office full-events or offsites. This is a remote position, so you'll be working remotely from your home. You may occasionally visit a GoDaddy office to meet with your team for events or offsites.

This position is not eligible to be performed in Alaska, Mississippi, North Dakota, or the Virgin Islands.

GoDaddy is not currently considering candidates for this role in California, Seattle, or NYC.

Join our team

Do you want to be an Information Security Leader at GoDaddy? GoDaddy's Product Security group is looking for a Principal Security Engineer to join our organization. Can you solve large scale and cross-company issues, while ensuring that partnership with the development and operational communities remains in front of mind?

GoDaddy is looking for a Principal Security Engineer to apply their hands-on technical skills, strong leadership abilities, and an eagerness to design solutions to complex problems. You must be comfortable with communicating to stakeholders, performing security assessments and prioritizing security risks, creating/presenting high-quality deliverables.

What you'll get to do...

Identify security threats in applications and infrastructure and provide remediation mentorship to system owners.
Join forces with SRE and development teams to find new and creative ways to reduce the occurrence of vulnerabilities at scale.
Build repeatable/reusable security processes and frameworks.
Review quality issues and work towards detecting security flaws both obvious and discrete.
Assist with scoping prospective projects, participating in projects from kickoff through "definition of done" via end-to-end ownership.
Use your industry experience to own and drive resolution and retest complex security events, policy questions and technical security risks.

Your experience should include...

7+ years of progressive security engineering experience across Security Architecture, Cryptography, Network, Cloud, Mobile, and Web Security.
Skilled in Secure Development Lifecycle, Security by Design, and Shift Left methodologies.
Proficient in Threat Modeling, Architecture Review, Penetration Testing, Code Review, SAST, and DAST.
Strong scripting abilities in languages such as Python, C, C++, Java, Ruby, and PowerShell.
Adept at applying security best practices for compliance, with excellent problem-solving and communication skills.

You might also have...

Bachelor's degree in computer science or related field.
Master's degree or PhD in Computer Science or related field.
Hosting industry and/or cloud Experience.
Experience in hardware security.

We've got your back... We offer a range of total rewards that may include paid time off, retirement savings (e.g., 401k, pension schemes), bonus/incentive eligibility, equity grants, participation in our employee stock purchase plan, competitive health benefits, and other family-friendly benefits including parental leave. GoDaddy's benefits vary based on individual role and location and can be reviewed in more detail during the interview process.

We also embrace our diverse culture and offer a range of Employee Resource Groups (Culture). Have a side hustle? No problem. We love entrepreneurs! Most importantly, come as you are and make your own way.

About us... GoDaddy is empowering everyday entrepreneurs around the world by providing the help and tools to succeed online, making opportunity more inclusive for all. GoDaddy is the place people come to name their idea, build a professional website, attract customers, sell their products and services, and manage their work. Our mission is to give our customers the tools, insights, and people to transform their ideas and personal initiative into success. To learn more about the company, visit About Us.

At GoDaddy, we know diverse teams build better products—period. Our people and culture reflect and celebrate that sense of diversity and inclusion in ideas, experiences and perspectives. But we also know that's not enough to build true equity and belonging in our communities. That's why we prioritize integrating diversity, equity, inclusion and belonging principles into the core of how we work every day—focusing not only on our employee experience, but also our customer experience and operations. It's the best way to serve our mission of empowering entrepreneurs everywhere, and making opportunity more inclusive for all. To read more about these commitments, as well as our representation and pay equity data, check out our Diversity and Pay Parity annual report which can be found on our Diversity Careers page.

GoDaddy is proud to be an equal opportunity employer. GoDaddy will consider for employment qualified applicants with criminal histories in a manner consistent with local and federal requirements. Refer to our full EEO policy.

Our recruiting team is available to assist you in completing your application. If they could be helpful, please reach out to

Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

GoDaddy doesn't accept unsolicited resumes from recruiters or employment agencies.

Remote working/work at home options are available for this role.

Not Specified

Lead Security Architect (Remote)

✦ New

🏢 GoDaddy

Salary not disclosed

Remote, Oregon 16 hours ago

Location Details: United States - Remote

At GoDaddy the future of work looks different for each team. Some teams work in the office full-events or offsites. This is a remote position, so you'll be working remotely from your home. You may occasionally visit a GoDaddy office to meet with your team for events or offsites.

This position is not eligible to be performed in Alaska, Mississippi, North Dakota, or the Virgin Islands.

GoDaddy is not currently considering candidates for this role in California, Seattle, or NYC.

Join our team

Do you want to be an Information Security Leader at GoDaddy? GoDaddy's Product Security group is looking for a Principal Security Engineer to join our organization. Can you solve large scale and cross-company issues, while ensuring that partnership with the development and operational communities remains in front of mind?

GoDaddy is looking for a Principal Security Engineer to apply their hands-on technical skills, strong leadership abilities, and an eagerness to design solutions to complex problems. You must be comfortable with communicating to stakeholders, performing security assessments and prioritizing security risks, creating/presenting high-quality deliverables.

What you'll get to do...

Identify security threats in applications and infrastructure and provide remediation mentorship to system owners.
Join forces with SRE and development teams to find new and creative ways to reduce the occurrence of vulnerabilities at scale.
Build repeatable/reusable security processes and frameworks.
Review quality issues and work towards detecting security flaws both obvious and discrete.
Assist with scoping prospective projects, participating in projects from kickoff through "definition of done" via end-to-end ownership.
Use your industry experience to own and drive resolution and retest complex security events, policy questions and technical security risks.

Your experience should include...

7+ years of progressive security engineering experience across Security Architecture, Cryptography, Network, Cloud, Mobile, and Web Security.
Skilled in Secure Development Lifecycle, Security by Design, and Shift Left methodologies.
Proficient in Threat Modeling, Architecture Review, Penetration Testing, Code Review, SAST, and DAST.
Strong scripting abilities in languages such as Python, C, C++, Java, Ruby, and PowerShell.
Adept at applying security best practices for compliance, with excellent problem-solving and communication skills.

You might also have...

Bachelor's degree in computer science or related field.
Master's degree or PhD in Computer Science or related field.
Hosting industry and/or cloud Experience.
Experience in hardware security.