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Biotech Process Development Jobs in Pawtucket, RI

Amgen

Specialist QC

West Greenwich, RI · On-site

Collaborate with Quality Control laboratories, Manufacturing, Process Development, Quality ... biotechnology or pharmaceutical industry. * Demonstrated experience leading complex laboratory ...

Amgen, Inc.

Specialist QC

West Greenwich, RI · On-site

Collaborate with Quality Control laboratories, Manufacturing, Process Development, Quality ... biotechnology or pharmaceutical industry. * Demonstrated experience leading complex laboratory ...

Amgen SA

Specialist QC

West Greenwich, RI · On-site

$95 - $125/hr

Collaborate with Quality Control laboratories, Manufacturing, Process Development, Quality ... biotechnology or pharmaceutical industry. * Demonstrated experience leading complex laboratory ...

New

Danaher

Filtration Sales Specialist

Providence, RI · Remote

$100K - $130K/yr

Process development with knowledge of clinical workflow * Commercial sales process, preferably in the Biotechnology industry. * Cross selling, upselling, value positions and funnel management. Cytiva ...

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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 Aug 20, 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 are popular job titles related to Biotech Process Development jobs in Pawtucket, RI?

For Biotech Process Development jobs in Pawtucket, RI, the most frequently searched job titles are:

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.

Team Leader, Formulation Manufacturing

Thermo Fisher Scientific

Plainville, MA • On-site

$66K - $99K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 427 frontline employees who took The Breakroom Quiz

199th of 542 rated manufacturers

Job description

Work Schedule
12 hr shift/days
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
Title: Team Leader, Formulation Manufacturing
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information
Reporting to the Plainville, MA site and supporting the Viral Vector Services (VVS), a division of Thermo Fisher Scientific. At VVS, we deliver from process development through commercial supply, offering the expertise and resources vital to help clients deliver innovative gene therapies. We are placed at the forefront of our leading and groundbreaking Cell and Gene Therapy business, enabling clients to cure genetic, rare, and otherwise untreatable diseases.
Work Schedule: 12 Hours, 2-2-3 schedule that runs 7am to 7pm (times may vary)
Discover Impactful Work:
As a Team Leader in Formulation Manufacturing at Thermo Fisher Scientific, you will guide a skilled team responsible for manufacturing high-quality pharmaceutical and biotechnology products while ensuring compliance with cGMP standards. You will support operational excellence through effective team leadership, process optimization, and cross-functional collaboration. This role combines technical expertise with people management to deliver important therapies that improve health outcomes.
A Day in the Life:
  • You will oversee daily manufacturing operations, coordinate production schedules, and ensure adherence to safety and quality standards.
  • The position involves supporting team members, troubleshooting equipment and processes, managing documentation, and implementing continuous improvement initiatives.
  • You'll work closely with Quality, Engineering, and other departments to maintain robust manufacturing processes and resolve technical challenges.
  • This role offers opportunities to make meaningful contributions to pharmaceutical development and commercial manufacturing while developing your leadership capabilities within an innovative organization.

Keys to Success:
Education
  • Bachelor's degree highly preferred. Preferred Fields of Study: Chemistry, Biochemistry, Biology, Engineering or related scientific field
  • High school diploma or equivalent required.
Experience
  • 2 years of pharmaceutical, or biotechnology manufacturing experience in cGMP environment required with a degree, and 3-4 years of experience in lieu of a degree.
  • Experience managing documentation, investigations, and change controls.
  • Experience with Lean manufacturing principles and continuous improvement methodologies.

Knowledge, Skills, Abilities
  • Strong knowledge of current Good Manufacturing Practices (cGMP) and regulatory requirements
  • Demonstrated ability to lead, mentor and develop manufacturing personnel
  • Excellent technical troubleshooting and process improvement capabilities
  • Strong project management and organizational skills
  • Proficiency with manufacturing systems, documentation, and Microsoft Office suite
  • Outstanding written and verbal communication skills
  • Ability to work rotating shifts including weekends/holidays as required
  • Physical ability to stand for extended periods and lift up to 50 pounds
  • Knowledge of cleanroom and aseptic techniques
  • Demonstrated commitment to safety culture and quality compliance
  • Strong problem-solving skills and attention to detail
  • Ability to collaborate effectively across functions

Benefits
We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.
Compensation and Benefits
The salary range estimated for this position based in Massachusetts is $66,000.00-$99,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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