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Research Development Process Engineer Jobs in Long Valley, NJ

Cellares

Senior Process Engineer

Bridgewater, NJ

$90K - $210K/yr

This position is responsible for supporting the activities involved in development, process ... researchers, and engineers) to develop the best solutions possible. The successful candidate will ...

Cellares

Senior Process Engineer

Bridgewater, NJ

$90K - $210K/yr

This position is responsible for supporting the activities involved in development, process ... researchers, and engineers) to develop the best solutions possible. The successful candidate will ...

Cellares

Senior Process Engineer

Bridgewater, NJ · On-site

$90K - $210K/yr

This position is responsible for supporting the activities involved in development, process ... researchers, and engineers) to develop the best solutions possible. The successful candidate will ...

Leidos

Process Engineer

Wharton, NJ · On-site

$69K - $125K/yr

The Defense Sector at Leidos currently has an opening for a Process Engineer to work at our Picatinny Arsenal, NJ site to Conduct process development and optimization for the preparation of ...

Leidos

Process Engineer

Wharton, NJ

$69K - $125K/yr

The Defense Sector at Leidos currently has an opening for a Process Engineer to work at our Picatinny Arsenal, NJ site to Conduct process development and optimization for the preparation of ...

Ubertal Inc

Process Engineer - MOCVD

Branchburg, NJ · On-site

Support MOCVD process manufacturing and engineering on multi-wafer production reactors for high-voltage device development * Develop MOCVD recipes aligned with device structures and design ...

Kenvue

Senior Scientist, Research & Development

Chatham, NJ · Hybrid

$105.40 - $148.80/hr

Bioinformatics programming software such as R and minitab * Detail-oriented and able to manage ... Peer reviewed publication and IP submission process with a proven track record of conducting and ...

Kenvue

Senior Scientist, Research & Development

Summit, NJ · Hybrid

$105.40 - $148.80/hr

Bioinformatics programming software such as R and minitab * Detail-oriented and able to manage ... Peer reviewed publication and IP submission process with a proven track record of conducting and ...

Kenvue

Senior Scientist, Research & Development

Summit, NJ · On-site

$105.40 - $148.80/hr

Bioinformatics programming software such as R and minitab * Detail-oriented and able to manage ... Peer reviewed publication and IP submission process with a proven track record of conducting and ...

Biztech Inc

Manufacturing Process Engineer

Denville, NJ · On-site

$125K - $140K/yr

We are seeking a hands-on Manufacturing Process Engineer to lead process improvement initiatives, optimize production operations, and support the development of world-class manufacturing processes.

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Showing results 21-40

All JobsResearch Development Process Engineer JobsResearch Development Process Engineer Jobs in Long Valley, NJ

Research Development Process Engineer information

See Long Valley, NJ salary details

$47.1K

$105.2K

$157.9K

How much do research development process engineer jobs pay per year?

As of Aug 10, 2026, the average yearly pay for research development process engineer in Long Valley, NJ is $105,227.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,400.00 and $123,200.00 per year, depending on experience, location, and employer.

What does a research development process engineer do?

A Research Development Process Engineer is responsible for designing, developing, and optimizing processes in research and product development settings. They work to improve efficiency, quality, and scalability of new products or technologies by bridging the gap between research and manufacturing. Their role often involves collaborating with scientists, engineers, and production teams to ensure that innovative concepts can be effectively and safely produced at a larger scale. They also analyze data, troubleshoot problems, and implement improvements to meet regulatory and business requirements.

What are the key skills and qualifications needed to thrive as a research development process engineer?

A Research Development Process Engineer requires a solid background in chemical or process engineering, problem-solving abilities, and typically a bachelor's or master's degree in a relevant field. Familiarity with process simulation software (such as Aspen Plus or MATLAB), statistical analysis tools, and industry-specific certifications like Six Sigma are often expected. Strong analytical thinking, teamwork, and effective communication distinguish top performers in this role. These skills ensure successful innovation, efficient process optimization, and seamless collaboration in research-driven engineering environments.

What are the main challenges research development process engineers face when transitioning projects from R&D to full-scale production?

One of the primary challenges Research Development Process Engineers encounter is ensuring that innovative processes developed in the laboratory can be effectively scaled up for manufacturing without compromising quality or efficiency. This often involves troubleshooting unforeseen issues, optimizing process parameters, and collaborating closely with cross-functional teams such as manufacturing, quality assurance, and supply chain. Navigating regulatory requirements and managing tight project deadlines are also common hurdles. Successful engineers leverage strong problem-solving skills and clear communication to bridge the gap between research concepts and practical, large-scale implementation.

What is the difference between Research Development Process Engineer vs Research Scientist?

AspectResearch Development Process EngineerResearch Scientist
Primary FocusDeveloping and optimizing manufacturing processes and workflowsConducting scientific research to generate new knowledge or products
Work EnvironmentIndustrial labs, manufacturing facilitiesAcademic or industrial research labs
Required CredentialsBachelor’s or Master’s in Engineering, Chemistry, or related fields; certifications in process improvementMaster’s or PhD in Science or Engineering
Industry UsageManufacturing, chemical, pharmaceutical industriesAcademic, R&D departments, biotech, pharmaceuticals

Research Development Process Engineers focus on translating research into scalable manufacturing processes, while Research Scientists primarily conduct experiments to advance scientific knowledge. Both roles require strong technical skills but differ in application and environment.

What cities near Long Valley, NJ are hiring for Research Development Process Engineer jobs? Cities near Long Valley, NJ with the most Research Development Process Engineer job openings:
Research Development Process Engineer jobs near you
Infographic showing various Research Development Process Engineer job openings in Long Valley, NJ as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $105,227 per year, or $50.6 per hour.

Senior Process Engineer

Cellares

Bridgewater, NJ

$90K - $210K/yr

Full-time

Re-posted 3 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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