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Senior Injection Molding Process Engineer Jobs in Bridgewater, NJ

Cellares

Senior Process Engineer

Bridgewater, NJ · On-site

$90K - $210K/yr

Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our MSAT team who will contribute significantly to the development of our advanced cell therapy ...

Cellares

Senior Process Engineer

Bridgewater, NJ

$90K - $210K/yr

Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our MSAT team who will contribute significantly to the development of our advanced cell therapy ...

Cellares

Senior Process Engineer

Bridgewater, NJ · On-site

$90K - $210K/yr

Position Summary We are seeking an innovative and highly motivated Senior Process Engineer on our MSAT team who will contribute significantly to the development of our advanced cell therapy ...

quip

Senior Product Quality Engineer

New York, NY · On-site

$135K - $175K/yr

DESCRIPTION quip is seeking a Senior Product Quality Engineer to own supplier quality ... High cavitation injection molding and machining process experience * Deep knowledge of materials ...

Biztech Inc

Manufacturing Process Engineer

Denville, NJ · On-site

$125K - $140K/yr

Senior Manufacturing Process EngineerDrive Continuous Improvement. Optimize Manufacturing. Make an Impact. We are seeking a hands-on Manufacturing Process Engineer to lead process improvement ...

quip

Senior Supplier Quality Engineer

New York, NY · On-site

$135K - $175K/yr

DESCRIPTION quip is seeking a Senior Supplier Quality Engineer to own supplier quality ... High cavitation injection molding and machining process experience * Deep knowledge of materials ...

Yespac

Be Seen First

Plastic Extruder Operator

Somerville, NJ · On-site

$20 - $25/hr

... molding, injection molding, or extrusion processes to optimize efficiency and product quality ... Familiarity with programmable logic controllers (PLCs) for machine automation control. * Bilingual ...

Urgent

Altium Packaging LLC

Machine Operator - 3rd Shift

Monroe, NJ · On-site

$17.50 - $21/hr

Operate blow-mold/PET/injection molding machines (including wheels, reciprocating or shuttle machines) to ensure production of quality bottles. * Adhere to quality control and to blow mold process ...

Kenvue

Senior Packaging Engineer

Summit, NJ · Hybrid

$90.10 - $127.20/hr

Leads process improvement or task teams. Partners with the creative design group to deliver ... Extrusion / Injection molding * Dispensing systems (airless, pumps, aerosols). * Paper and ...

Kenvue

Senior Packaging Engineer

Springfield, NJ · Hybrid

$90.10 - $127.20/hr

Leads process improvement or task teams. Partners with the creative design group to deliver ... Extrusion / Injection molding * Dispensing systems (airless, pumps, aerosols). * Paper and ...

Kenvue

Senior Packaging Engineer

Chatham, NJ · Hybrid

$90.10 - $127.20/hr

Leads process improvement or task teams. Partners with the creative design group to deliver ... Extrusion / Injection molding * Dispensing systems (airless, pumps, aerosols). * Paper and ...

Kenvue

Senior Packaging Engineer

Short Hills, NJ · Hybrid

$90.10 - $127.20/hr

Leads process improvement or task teams. Partners with the creative design group to deliver ... Extrusion / Injection molding * Dispensing systems (airless, pumps, aerosols). * Paper and ...

Kenvue

Senior Packaging Engineer

Mountainside, NJ · Hybrid

$90.10 - $127.20/hr

Leads process improvement or task teams. Partners with the creative design group to deliver ... Extrusion / Injection molding * Dispensing systems (airless, pumps, aerosols). * Paper and ...

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Showing results 21-40

All JobsInjection Molding Process Engineer JobsSenior Injection Molding Process Engineer JobsSenior Injection Molding Process Engineer Jobs in Bridgewater, NJ

Senior Injection Molding Process Engineer information

See Bridgewater, NJ salary details

$76.7K

$123.8K

$174.3K

How much do senior injection molding process engineer jobs pay per year?

As of Aug 8, 2026, the average yearly pay for senior injection molding process engineer in Bridgewater, NJ is $123,808.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,300.00 and $137,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a senior injection molding process engineer?

To thrive as a Senior Injection Molding Process Engineer, you need a deep understanding of polymer science, mold design, process optimization, and typically a degree in engineering or a related field. Expertise with CAD software, process simulation tools, and familiarity with quality systems like ISO 9001 are commonly required, along with certifications such as RJG or Six Sigma. Strong analytical thinking, problem-solving abilities, and effective communication are essential soft skills for collaborating with cross-functional teams and troubleshooting production issues. These skills ensure efficient production, high-quality output, and continuous improvement in complex manufacturing environments.

What does a senior injection molding process engineer do?

A Senior Injection Molding Process Engineer is responsible for designing, optimizing, and troubleshooting the injection molding process used to manufacture plastic parts. They oversee process improvements, ensure product quality, and collaborate with cross-functional teams to meet production goals. Additionally, they may develop and implement new molding technologies, train staff, and support maintenance of equipment to ensure efficient and reliable operations.

What is the difference between Senior Injection Molding Process Engineer vs Injection Molding Technician?

AspectSenior Injection Molding Process EngineerInjection Molding Technician
CredentialsBachelor's degree in engineering or related field, certifications in process optimizationTechnical diploma or associate degree, on-the-job training
Work EnvironmentDesigning processes, analyzing data, improving production efficiencyOperating machinery, performing setup and maintenance
ResponsibilitiesProcess development, troubleshooting, process validationMachine operation, quality checks, routine maintenance

The Senior Injection Molding Process Engineer focuses on process design, optimization, and troubleshooting, requiring higher-level technical skills and education. In contrast, the Injection Molding Technician handles daily machine operation and maintenance tasks. Both roles are essential in the manufacturing environment but differ in scope and responsibilities.

What are the common challenges faced by senior injection molding process engineers when introducing a new mold into production?

Senior Injection Molding Process Engineers often encounter challenges such as optimizing process parameters for new molds, ensuring part quality meets specifications, and troubleshooting issues like warpage or incomplete filling. Collaboration with design, tooling, and quality teams is essential to address these challenges and implement effective solutions quickly. Additionally, balancing production efficiency with consistent quality requires careful monitoring and adjustment during the initial production runs.
What cities near Bridgewater, NJ are hiring for Senior Injection Molding Process Engineer jobs? Cities near Bridgewater, NJ with the most Senior Injection Molding Process Engineer job openings:
Senior Injection Molding Process Engineer jobs near you
Infographic showing various Senior Injection Molding Process Engineer job openings in Bridgewater, NJ as of June 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $123,808 per year, or $59.5 per hour.

Senior Process Engineer

Cellares

Bridgewater, NJ • On-site

$90K - $210K/yr

Full-time

Re-posted 8 hours ago

Job description

Position Summary
 
 
We are seeking an innovative and highly motivated Senior Process Engineer on our MSAT team who will contribute significantly to the development of our advanced cell therapy manufacturing platform. 
 
This position is responsible for supporting the activities involved in development, process transfers, compliance, and scalability for Cellares' manufacturing operations. This individual will focus on technology transfers from Process Development into GMP manufacturing facilities, as well as driving and developing process automation and scalability solutions to improve process reliability, safety, cost-effectiveness, scalability, and compliance. 
 
This is a multidisciplinary role & this individual will interface across many parts of the company (with customers, scientists, researchers, and engineers) to develop the best solutions possible. The successful candidate will be a resident expert in the areas of technology transfer and manufacturing science and technology. It is expected that this individual will work closely with other corporate functional areas and partners to ensure deliverables are met. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.
Responsibilities
  • Work to identify and communicate standards and best practices for process design and manufacturing to ensure consistency across manufacturing of cell therapies
  • Work as the MSAT representative on client projects
  • Lead activities to transfer processes to manufacturing from internal Cellares process development at other sites or directly from customers
  • Lead Master Validation Plan creation in order to support PPQ campaigns  
  • Lead and drive technology adoption program initiatives, including ROI analyses with internal and external stakeholders
  • Support development of manufacturing operations including GMP system implementation and tasks related to GMP readiness
  • Support process development and process comparability activities on Cellares technology as required
  • Support development and review of relevant SOPs for manufacturing operations and systems. Author and review global program policies  Perform manufacturability assessments for new process introductions
  • Define and provide user requirements for process equipment associated with multiple facilities for the manufacture of cell therapies
  • Work with our software team on integration solutions for the manufacturing process and data management, including eBR, MES, QMS, and LIMS
  • Work with our software team to provide feedback on internal software solutions
  • Provide technical support to Manufacturing and other departments associated with GMP operations
  • Support or author product quality impact assessment  for major deviations. Provide input when troubleshooting processes on the manufacturing floor and during post-operational investigations
  • Maintain and report process run summaries, and continued process verification reports
  • Prepare and present data associated with manufacturing processes to internal and external partners
  • Support for process qualification and validation preparation, execution, and reporting
  • Work with clients on process mapping of the manufacturing processes
  • Other duties as assigned
Requirements
  • Bachelor's Degree in a scientific or related field is required
  • A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy
  • Experience in the Pharma/Biotech industry in technology transfer
  • Must know and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries. Must comply with safety policies of the company and site
  • Adherence to cGMPs is required all times during the manufacture of Cell Therapy products. All personnel are responsible for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, product defects and related actions
  • Relevant experience bringing biotechnology equipment and processes from design through GMP operational readiness is a plus
  • Must have experience writing, reviewing and approving GMP documentation
  • Self-motivated and passionate about advancing the field of cell therapy
  • Self-awareness, integrity, authenticity, and a growth mindset
  • Desire to be part of a rapidly evolving organization, with a compelling technology, and taking products and processes to the next level 
  • Excellent planning, organization, technical writing, and time-management skills including the ability to support, problem-solve, and prioritize multiple projects and deadlines.
 
$90,000 - $210,000 a year
This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company's Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares' Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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About Cellares

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

11 - 50 Employees

Headquarters location

South San Francisco, CA, US

Year founded

2019

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