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Senior Manufacturing Process Engineer Jobs in Parlin, 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 ... This individual will focus on technology transfers from Process Development into GMP manufacturing ...

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 ... This individual will focus on technology transfers from Process Development into GMP manufacturing ...

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 ... This individual will focus on technology transfers from Process Development into GMP manufacturing ...

Amazon

Senior Manufacturing Engineer, Fauna

New York, NY · On-site

$99K - $136K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Fauna is seeking a Senior Manufacturing Engineer to help concept, design, and scale assembly ... Think of the factory as a fully integrated product - best part/process is no part/process. - Drive ...

Amazon

Senior Manufacturing Engineer, Fauna

New York, NY · On-site

$99K - $136K/yr

Fauna is seeking a Senior Manufacturing Engineer to help concept, design, and scale assembly ... Think of the factory as a fully integrated product - best part/process is no part/process. - Drive ...

Amazon

Senior Manufacturing Engineer, Fauna

New York, NY

$99K - $136K/yr

Fauna is seeking a Senior Manufacturing Engineer to help concept, design, and scale assembly ... Think of the factory as a fully integrated product - best part/process is no part/process. - Drive ...

Rocket Pharmaceuticals

Senior Process Engineer, MS&T

Cranbury, NJ · On-site

$118K - $178K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Manufacturing Science & Technology (MS&T) function is seeking a highly motivated Senior Process Engineer to be responsible for early and late stage AAV development, commercialization, and ...

Johns Manville

Process Engineer

Edison, NJ · On-site

$94K - $129K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Who We Are Johns Manville is a leading manufacturer and marketer of premium-quality insulation and ... The purpose of the Process Engineer's role will be to provide technical leadership to operate a ...

Jm

Process Engineer

Edison, NJ · On-site

$94K - $129K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Who We Are Johns Manville is a leading manufacturer and marketer of premium-quality insulation and ... The purpose of the Process Engineer's role will be to provide technical leadership to operate a ...

Raycap Inc

Process Engineer

Kearny, NJ · On-site

  • Retirement

  • PTO

Job Overview The Process Engineer will be responsible for improvements relating to industrial/manufacturing processes and efficiency to reduce costs, improve sustainability, and maximize ...

CompoSecure

Lead Process Engineer

Somerset, NJ · On-site

$109K - $142K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Perform statistical analysis of manufacturing yields to identify performance gaps, drive continuous ... Prepare and present technical proposals and improvement plans to senior leadership, championing ...

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All JobsManufacturing Process Engineer JobsSenior Manufacturing Process Engineer JobsSenior Manufacturing Process Engineer Jobs in Parlin, NJ

Senior Manufacturing Process Engineer information

See Parlin, NJ salary details

$77.2K

$124.7K

$175.6K

How much do senior manufacturing process engineer jobs pay per year?

As of Aug 18, 2026, the average yearly pay for senior manufacturing process engineer in Parlin, NJ is $124,719.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,100.00 and $138,500.00 per year, depending on experience, location, and employer.

What does a senior manufacturing process engineer do?

A Senior Manufacturing Process Engineer is responsible for designing, analyzing, and improving manufacturing processes to increase efficiency, quality, and safety in production environments. They lead projects to implement new technologies, troubleshoot process issues, and optimize workflows. They also work closely with cross-functional teams to ensure that products meet industry standards and regulatory requirements. Additionally, they mentor junior engineers and support continuous improvement initiatives within the organization.

What are the main challenges a senior manufacturing process engineer faces when implementing process improvements?

One of the primary challenges Senior Manufacturing Process Engineers encounter is balancing the need for process innovation with maintaining production efficiency and product quality. Implementing new technologies or methodologies often requires extensive cross-functional collaboration, training, and sometimes overcoming resistance to change from team members. Additionally, ensuring that process improvements comply with industry regulations and safety standards can add complexity. However, these challenges provide valuable opportunities to develop leadership skills and drive significant impact within the organization.

What are the key skills and qualifications needed to thrive as a senior manufacturing process engineer, and why are they important?

To thrive as a Senior Manufacturing Process Engineer, you need a strong background in engineering principles, process optimization, and manufacturing systems, typically with a bachelor's or master's degree in engineering and relevant industry experience. Familiarity with CAD/CAM software, Lean Six Sigma methodologies, and statistical process control tools is highly valued, along with certifications such as Six Sigma Green or Black Belt. Exceptional problem-solving abilities, leadership, and effective communication are crucial soft skills for driving process improvements and collaborating across teams. These skills ensure efficient production, high product quality, and continuous operational enhancements in a competitive manufacturing environment.

What is the difference between Senior Manufacturing Process Engineer vs Manufacturing Engineer?

AspectSenior Manufacturing Process EngineerManufacturing Engineer
Required CredentialsBachelor's degree in engineering, 5+ years experience, possibly certifications like Six SigmaBachelor's degree in engineering or related field, 1-3 years experience
Work EnvironmentOversees process improvements, leads projects, collaborates with cross-functional teamsSupports manufacturing operations, implements process changes, troubleshoots production issues
Employer & Industry UsageUsed in manufacturing plants, automotive, aerospace, electronics industriesCommon in similar industries, entry to mid-level roles in manufacturing

The main difference is that a Senior Manufacturing Process Engineer typically has more experience, takes on leadership roles, and oversees complex process improvements, while a Manufacturing Engineer focuses on supporting and implementing manufacturing processes at a more operational level.

What are popular job titles related to Senior Manufacturing Process Engineer jobs in Parlin, NJ?

For Senior Manufacturing Process Engineer jobs in Parlin, NJ, the most frequently searched job titles are:

What cities near Parlin, NJ are hiring for Senior Manufacturing Process Engineer jobs?

Cities near Parlin, NJ with the most Senior Manufacturing Process Engineer job openings:

Senior Manufacturing Process Engineer jobs near you
Infographic showing various Senior Manufacturing Process Engineer job openings in Parlin, NJ as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $124,719 per year, or $60 per hour.

Senior Process Engineer

Cellares

Bridgewater, NJ • On-site

$90K - $210K/yr

Full-time

Re-posted 10 days 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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