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Contract Msat Process Engineer Jobs (NOW HIRING)

Evotec WD

Process Engineer III, Global MSAT

Redmond, WA · On-site

$92K - $126K/yr

Process Engineer III Location: Redmond, WA Reports To: Director, Global MSAT About Us Just‑Evotec Biologics is a forward‑thinking team in the biopharmaceutical sector that thrives on challenging ...

Evotec

Process Engineer III, Global MSAT

Redmond, WA · On-site

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 ...

Cellares

Senior Process Engineer

South San Francisco, CA · On-site

$125K - $161K/yr

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

Lonza

Associate Director, MSAT

Walkersville, MD · On-site +1

$174K - $203K/yr

Associate Director, MSAT Location: This position is currently remote. A future transition to an on ... Partner with Engineering, Manufacturing, Quality, Automation, and EHS teams to ensure process ...

Begell House Inc.

Site Process Engineer

Bend, OR · On-site

You will support tech transfer, scale-up, and validation of clinical and commercial processes, partnering closely with Manufacturing, QA, MSAT, and Engineering. This role offers exposure to advanced ...

Kinetic Personnel Group

Downstream Process

Tustin, CA · On-site

This role will partner with Manufacturing, Process Development, Quality, and MSAT teams to analyze ... Chemical Engineering Biochemistry Biology Biotechnology Biomedical Engineering Biochemical ...

Evotecgroup

Process Engineer 2

Redmond, WA · On-site

Process Engineer II Location: Redmond, WA Department ... Global MSAT Reports To: Director, GMSAT About Us: this is who we are At Just Evotec Biologics , we ...

Evotec WD

Process Engineer 2

Redmond, WA · On-site

Process Engineer II Location: Redmond, WA Department ... Global MSAT Reports To: Director, GMSAT About Us this is who we are At Just Evotec Biologics, we ...

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Contract Msat Process Engineer information

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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?

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

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Contract Msat Process Engineer jobs near you

Process Engineer II, MSAT

Gainesville, FL • On-site

Kincell Bio, LLC
See more jobs at Kincell Bio, LLCexternal

Full-time

Posted 5 days ago

Job description

Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance.
For more information, please visit our website at www.kincellbio.com.
Kincell is seeking a Process Engineer II who will lead complex technical work across multiple cell therapy unit operations or an integrated process segment. The role leads investigations, process characterization, technology transfer execution, validation activities, and cross-functional improvement initiatives while serving as a trusted technical resource to Manufacturing, Quality, and clients.
Role mission: Lead technical improvements across multiple interconnected unit operations and drive process robustness, transfer, and validation execution.
Essential Duties and Responsibilities
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.
  • Provide technical ownership for multiple interconnected unit operations or a complete upstream or downstream process segment.
  • Lead complex deviation investigations and root cause analyses using structured tools such as 5-Why, fishbone, fault tree, and risk assessment.
  • Plan and lead process characterization, engineering, comparability, and optimization studies using sound experimental design.
  • Lead technology transfer execution, including gap assessment, facility fit, equipment fit, process risk assessment, readiness planning, and transfer documentation.
  • Develop or lead process validation protocols, reports, acceptance criteria, and supporting risk assessments.
  • Apply statistical methods such as DOE, SPC, capability analysis, and multivariate trending to improve process understanding and control.
  • Lead cross-functional process improvement initiatives focused on yield, robustness, cycle time, contamination control, and right-first-time performance.
  • Assess new equipment, single-use systems, raw materials, and manufacturing technologies and recommend implementation strategies.
  • Author and approve technical content in SOPs, MBRs, protocols, reports, Change Controls, and regulatory support documents.
  • Represent MSAT in regular client technical meetings and communicate risks, data, decisions, and recovery plans clearly.
  • Mentor Associate Process Engineers and Process Engineers I through technical coaching and review of deliverables.
  • Support audits, inspections, and program governance as a subject-matter expert for assigned processes.
Qualifications
The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.
Required:
  • Bachelor's degree in Engineering, Biology, Biotechnology, Life Sciences, or a related discipline with 4+ years of relevant experience; advanced degree may substitute for a portion of experience.
  • Demonstrated experience leading investigations, engineering studies, technology transfer, validation, or process improvement in a GMP environment.
  • Strong understanding of cell therapy manufacturing, aseptic processing, contamination control, and process risk management.
  • Ability to manage multiple priorities and lead cross-functional technical projects with limited supervision.
  • Strong technical writing, data analysis, presentation, and client communication skills.
Preferred:
  • Experience with CAR-T, CAR-NK, CAR-M, TIL, gene-edited cell therapy, or related immune cell platforms.
  • Advanced proficiency in statistical software and experimental design.
  • Experience with client-facing CDMO work, regulatory submissions, comparability, or process performance qualification.
Physical Requirements / Work Environment:
  • Ability to work in GMP cleanroom environments (ISO 5-8) while wearing required PPE and gowning for extended periods.
  • Ability to stand, walk, bend, reach, and perform repetitive hand movements during manufacturing support activities.
  • Ability to lift, push, pull, and transport materials or equipment up to 25 pounds routinely and up to 40 pounds occasionally with assistance, if required.
  • Ability to visually inspect equipment, labels, batch records, and technical documentation with attention to detail.
  • Ability to support flexible scheduling, including occasional weekends, holidays, extended operations, or shift-based manufacturing support as required.
Travel Requirements
  • Little to none; occasional travel may be required for client support, vendor activities, or technology transfer from client or between company sites.
Location
  • This position is 100% on-site in Gainesville, Florida and may require frequent non-standard working hours, including scheduled early mornings, late evenings, and/or weekends.

#LI-Onsite
Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.

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