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Biotech Process Development Jobs in Pawtucket, RI

Syner-G

Process Engineer

Plainville, MA · On-site

This role requires extensive cross-functional collaboration with Process Development, Manufacturing ... pharmaceutical/biotech or medical device manufacturing environments Technical Experience:

Pharmaron

Senior Scientist, Process Chemistry

Coventry, RI · On-site

$100K - $130K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Lead API manufacturing technology transfer, process development, and process improvement to ...

Pharmaron

Senior Scientist, Process Chemistry

Coventry, RI · On-site

$100K - $130K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Lead API manufacturing technology transfer, process development, and process improvement to ...

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Biotech Process Development information

See Pawtucket, RI salary details

$18

$32

$48

How much do biotech process development jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for biotech process development in Pawtucket, RI is $32.78, according to ZipRecruiter salary data. Most workers in this role earn between $26.92 and $40.24 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 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 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 job categories do people searching Biotech Process Development jobs in Pawtucket, RI look for?

The top searched job categories for Biotech Process Development jobs in Pawtucket, RI are:

Biotech Process Development jobs near you
Infographic showing various Biotech Process Development job openings in Pawtucket, RI as of June 2026, with employment types broken down into 1% As Needed, 80% Full Time, 16% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $68,175 per year, or $32.8 per hour.

Director, Downstream Process Development and Manufacturing Biologics

Bridgewater, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 11 days ago

Job description

About The Role

Director, Downstream Process Development and Manufacturing Biologics (Technical Operations CMC) reporting to the Executive Director, Pharmaceutical Development.

What You'll Do
  • Lead end-to-end downstream process development across unit operations, including viral clearance, process characterization (QbD), process validation, and BLA-enabling activities for clinical/commercial manufacturing.
  • Develop and implement phase-appropriate downstream purification strategies for early/late-stage pipeline projects.
  • Direct development and transfer of processes to Contract Manufacturing Organizations (CMOs); oversee scale-up to pilot/GMP commercial production.
  • Provide technical oversight and direction to CDMO partners to ensure robust, scalable, compliant manufacturing.
  • Define and oversee viral safety strategies (viral inactivation, viral filtration (VF), chromatography-based clearance).
  • Supervise development of filtration (VF, UFDF) and chromatography steps; implement QbD for characterization and validation.
  • Stay current on emerging downstream process technologies.
  • Author/review technical documents including BLA filings, CMC sections, and viral clearance studies.
  • Coach, mentor, and provide technical guidance.
  • Collaborate cross-functionally to align technical strategies with organizational/business objectives.
Who You Are (Qualifications)
  • PhD with at least 5 years industry experience, or MS with at least 8 years industry experience.
  • Downstream process development and manufacturing of biologics (antibodies, ADC, fusion proteins).
  • Deep experience with chromatography systems, filtration, viral inactivation/removal, and CDMO management.
  • Experience/knowledge in process characterization and process validation.
  • Extensive understanding of cGMP regulations and ICH guidelines.
  • Ability to work collaboratively using diverse perspectives.
Nice to Have
  • Degree in Chemical Engineering, Biotechnology, or relevant scientific field.
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