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Contract Msat Process Engineer Jobs (NOW HIRING)

Process Engineer, MSAT

Bedford, MA · On-site

$94K - $125K/yr

This position will serve as a mid-level engineer focused on drug product and process development in the Manufacturing Sciences and Technology (MSAT) department. This engineer will join a team in the ...

MS&T organization is seeking to fill a Process Engineer position for an 8+ month contract. * The ... Manufacturing Technical Support (MTS), Manufacturing Sciences & Technology (MS&T/MSAT), process ...

Position Summary AskBio is seeking a Process Engineer II to join our MSAT Process Engineering team ... the MSAT laboratory, perform scale-up runs, and transfer programs to AskBio's contract ...

Position Summary AskBio is seeking a Process Engineer II to join our MSAT Process Engineering team ... the MSAT laboratory, perform scale-up runs, and transfer programs to AskBio's contract ...

Syner-G is seeking a highly experienced Staff Process Engineer / MSAT Technology Transfer Lead with 10-15+ years of biologics manufacturing experience to provide technical and program leadership for ...

Syner-G is seeking a highly experienced Staff Process Engineer / MSAT Technology Transfer Lead with 10-15+ years of biologics manufacturing experience to provide technical and program leadership for ...

Process Engineer III Location: Redmond, WA Reports To: Director, Global MSAT About Us: At Just-Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a ...

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Contract Msat Process Engineer information

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$142.5K

How much do contract msat process engineer jobs pay per year?

As of Sep 15, 2026, the average yearly pay for contract msat process engineer in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What is a Contract MSAT Process Engineer?

A Contract MSAT (Manufacturing Science and Technology) Process Engineer is a professional who works on a temporary or project-based contract to support the development, optimization, and troubleshooting of manufacturing processes in industries such as pharmaceuticals or biotechnology. Their primary role is to ensure processes are efficient, compliant, and capable of producing high-quality products. They often collaborate with other departments, such as quality assurance and production, to implement process improvements, technology transfers, and scale-up activities. Contract positions typically mean the engineer is hired for a specific project or period rather than as a permanent employee.

What are the key skills and qualifications needed to thrive as a Contract MSAT Process Engineer?

To thrive as a Contract MSAT (Manufacturing Science and Technology) Process Engineer, you need a strong background in chemical or biochemical engineering, process optimization, and a relevant engineering degree. Familiarity with process simulation software (like Aspen or SuperPro), statistical analysis tools, and regulatory compliance standards such as cGMP is typically required. Excellent problem-solving, communication, and project management skills help drive cross-functional collaboration and process improvements. These competencies ensure efficient, compliant manufacturing processes and successful technology transfer in a highly regulated industry.

What are some common challenges faced by Contract MSAT Process Engineers during technology transfer projects?

Contract MSAT Process Engineers often encounter challenges such as aligning process specifications between sending and receiving sites, troubleshooting unexpected deviations during scale-up, and ensuring thorough documentation for regulatory compliance. Communication with cross-functional teams—including manufacturing, quality assurance, and R&D—is critical to anticipate and resolve issues quickly. Additionally, adapting to varying site capabilities and timelines requires strong project management and flexibility to deliver successful technology transfers.

What is the difference between Contract Msat Process Engineer vs Contract Chemical Process Engineer?

AspectContract Msat Process EngineerContract Chemical Process Engineer
CredentialsBachelor's in Chemical Engineering or related, certifications varyBachelor's in Chemical Engineering or related, certifications vary
Work EnvironmentManufacturing plants, chemical facilities, process optimizationRefineries, chemical plants, process design and improvement
Industry UsageOil & gas, petrochemicals, manufacturingChemical manufacturing, refining, pharmaceuticals

The Contract Msat Process Engineer and Contract Chemical Process Engineer roles share similar educational backgrounds and work environments, often within chemical and manufacturing industries. The main difference lies in their specific focus areas: Msat Process Engineers typically concentrate on process optimization and safety in manufacturing, while Chemical Process Engineers may focus more on process design and chemical reactions. Both roles require relevant engineering credentials and are vital in their respective sectors.

What cities are hiring for Contract Msat Process Engineer jobs?

Cities with the most Contract Msat Process Engineer job openings:

What are the most commonly searched types of Msat Process Engineer jobs?

The most popular types of Msat Process Engineer jobs are:

What states have the most Contract Msat Process Engineer jobs?

States with the most job openings for Contract Msat Process Engineer jobs include:

What are popular job titles related to Contract Msat Process Engineer jobs?

For Contract Msat Process Engineer jobs, the most frequently searched job titles are:

Process Engineer, MSAT

Bedford, MA • On-site

Ocular Therapeutix
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees

$94K - $125K/yr

Full-time

Re-posted 21 days ago


Job description

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space.
Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity.
Position Summary:
This position will serve as a mid-level engineer focused on drug product and process development in the Manufacturing Sciences and Technology (MSAT) department. This engineer will join a team in the clinical and commercial development of the processes used to manufacture sustained release hydrogel drug products. This role includes but is not limited to experimental design, process development, packaging, inspection and material characterization. This individual will execute some assigned project activities, lead some project activities, and work with team members to improve, evaluate, and develop the products and their associated processes. This engineer will be supporting the integration of a drug product with a medical device to produce a combination product. The position is set in a dynamic and fast-paced environment at a growing company.
Critical areas of focus will be in experimental design, laboratory work, testing, technical transfers, scale-up and new process development. Incorporation of automation into a complex manual process will be another area of focus for this engineer. This position will be based full-time onsite in Bedford, MA.
Principal Duties and Responsibilities:
  • Design, develop, execute and characterize process development studies.
  • Design and develop unit operations of a scalable commercial manufacturing process.
  • Execute improvement of current clinical and commercial manufacturing activities.
  • Implement and integrate automated systems into a complex manual process.
  • Assist in the cGMP manufacturing of drug product batches in clean room environment to support clinical studies.
  • Understand GMP regulation and FDA/EMEA guidance on manufacturing processes and apply them during manufacturing of combination product batches.
  • Analyze and evaluate the impact of process variables on combination product characteristics.
  • Communicate study designs, data analysis and conclusions to project team members.
  • Generate technical documents including protocols and reports summarizing experimental plans and test results.
  • Collaborate effectively with MSAT group and project team members.
  • Serve as an MSAT SME in cross-functional interactions with other departments.
  • Demonstrate an understanding of late-stage combination product development and tech transfer needs of commercial development.

Requirements:
  • Minimum of a bachelor's degree (advanced degree desirable) in Chemical Engineering, Biomedical Engineering, Mechanical Engineering or related discipline.
  • 4+ years of biopharma industry experience in drug or combination process development.
  • Prior experience working within a cGMP manufacturing environment.
  • Ability to apply fundamental scientific and engineering skills to evaluation of processes and development of practical solutions to technical challenges.
  • Experience creating technical, written content.
  • Demonstrated written and verbal communication skills.
  • Demonstrated data analysis and problem-solving skills.
  • High degree of initiative and self-motivation.
  • A diligent team-player that is passionate about helping patients and effectively collaborates in a dynamic, cross-functional environment.
  • Experience with generic lab equipment (Ex. pipettes, balances, pumps, microscopes) is preferred.
  • Experience with automated or manual inspection systems is preferred.

Working Conditions:
  • Production Floor - gowning/cGMP requirements.
  • Laboratory/Clean Room - bending/lifting requirements.

#LI-LM1
Salary Range
$94,000-$125,000 USD
Ocular Therapeutix is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws regarding nondiscrimination. Ocular Therapeutix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or status as a veteran. For information on how Ocular Therapeutix collects, stores, and utilizes candidate information please see our privacy policy found at https://www.ocutx.com/privacy-policy/. For the Privacy Notice for California Job Applicants, please see CCPA Applicant Notice.