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Biotech Process Development Jobs in Massachusetts

Integrated Resources INC

Process Associate

Andover, MA · On-site

Required a Manufacturing Process Technician in a large scale biotech manufacturing facility This position is a temporary contract working on a 12 hour shift (6am - 6pm.) Includes some weekend work ...

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Biotech Process Development information

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$20

$34

$46

How much do biotech process development jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for biotech process development in Massachusetts is $34.37, according to ZipRecruiter salary data. Most workers in this role earn between $29.95 and $37.93 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
What are popular job titles related to Biotech Process Development jobs in Massachusetts? For Biotech Process Development jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Massachusetts look for? The top searched job categories for Biotech Process Development jobs in Massachusetts are:
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Biotech Process Development jobs near you
Senior Associate Process Engineer (Contract)

Senior Associate Process Engineer (Contract)

ElevateBio

Waltham, MA • On-site

$43 - $57/hr

Contractor

Re-posted yesterday

Job description

ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.
The Role:
ElevateBio is looking for a Senior Associate Process Engineer within the Manufacturing Science and Technology (MSAT) organization. As a Senior Associate Process Engineer in MSAT, you will provide process science support for GMP manufacturing, technology transfers, development studies, characterization, validation, and continuous improvement projects within a highly matrixed cross-functional team for ElevateBio programs. As part of support, you will write protocols, product impact assessments, root-cause analysis reports, and technical reports. You will additionally support data collection and charting for non-GMP and GMP batches. This position is a 6-month contract.
Here's What You'll Do:
  • Work cross-functionally across Process Development, Manufacturing, Quality, and Supply Chain to provide support for technology transfers and cGMP manufacturing for both clinical and commercial stage programs across modalities including cell and gene therapy, mRNA and viral vector.
  • Authoring and reviewing technical documentation related to manufacturing activities including protocols, technical reports, work instructions, SOPs.
  • Own and support quality events such as deviations, investigations, CAPAs, and Change Controls.
  • Assist in the root cause determination of process-related deviations in a timely and complete manner. The candidate will work with a cross-functional team to resolve complex problems using experience and efficient application of scientific methodology and technical reasoning, then propose comprehensive process solutions and improvements.
  • Support gap analyses and risk assessments to support the capital projects and tech transfers.

Requirements:
  • Bachelor's Degree in Life Sciences, Engineering, Biotechnology, or a related technical discipline
  • 3+ years of experience in a MSAT, Manufacturing, or Process Development role
  • Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell culture, and process development
  • Experience in cell and gene therapy, aseptic processing, and drug manufacturing preferred
  • Understanding of process development, validation, and lifecycle management to support comparability studies, process validation, and licensure changes
  • Strong communication skills and ability to work cross-functionally with technical and quality teams
  • Familiarity with electronic systems used in GMP environments such as Veeva, or electronic batch records

The budgeted range for this position is $43/hour - $57/hour. This range is a good faith estimate of the expected hourly range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.
ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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