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Biotech Process Development Jobs in Rhode Island

... 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 ...

... 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 ...

... 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 ...

Process Engineer

Coventry, RI ยท On-site

$90K - $130K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Support technology transfer projects from development through manufacturing implementation.

Process Engineer

Coventry, RI ยท On-site

$90K - $140K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Support technology transfer projects from development through manufacturing implementation.

Process Engineer

Coventry, RI ยท On-site

$90K - $140K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Support technology transfer projects from development through manufacturing implementation.Generate ...

Process Engineer

Coventry, RI ยท On-site

$90K - $130K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Support technology transfer projects from development through manufacturing implementation.

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Biotech Process Development information

See Rhode Island salary details

$18

$31

$42

How much do biotech process development jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for biotech process development in Rhode Island is $31.14, according to ZipRecruiter salary data. Most workers in this role earn between $27.16 and $34.38 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 Rhode Island look for?

The top searched job categories for Biotech Process Development jobs in Rhode Island are:

What cities in Rhode Island are hiring for Biotech Process Development jobs?

Cities in Rhode Island with the most Biotech Process Development job openings:

Associate Principal Scientist, Process Development

Coventry, RI โ€ข On-site

Pharmaron
Chemical Manufacturingย โ€ขย 10K+ employees

$120K - $160K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago


Key responsibilities

  • Solve high complexity chemical development issues for assigned projects and initiatives.

  • Design, execute, and interpret core experiments to support development and scale-up of chemical processes.

  • Communicate and collaborate with cross-functional teams to document results and contribute to reports, manuscripts, and presentations.


Job description

Position: Associate Principal Scientist, Process DevelopmentSalary Range: $120,000 - $160,000Location: Coventry, RI (On-site)About PharmaronPharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.What You'll DoAs a subject matter expert, the Associate Principal Scientist will solve high complexity chemical development issues for assigned projects and/or initiatives.Key ResponsibilitiesIn a multidisciplinary environment, solve problems of higher complexity for assigned projects and / or initiatives with limited guidance from a scientific supervisor / Line Manager.Fully competent in the core chemistry laboratory skills required to support development and / or scale up of chemical processes. Such skills include, but are not limited to, expert application of core laboratory techniques and instrumentation to positively impact API drug development. From time to time use of selected higher end instrumentation or methodologies with supervisor guidance may be required.Design and execute core experiments, interpret results, and plan additional experiments in a timely manner to solve assigned problems of high complexity.Actively participate in the development of new technologies or methodologies, as appropriate within the functional area.Effectively communicate, coordinate and collaborate with cross-functional project groups to ensure that scientific work is appropriately documented such that the broader collaborative inputs and efforts are combined to maximum effect in the production of reports, manuscripts, and presentations.Document and report results of all experiments in a manner consistent with department practices and governing policies, as applicable, which may include significant contributions to manufacture of API for GLP toxicology studies or for GMP manufacture of clinical supplies.Contribute to effective team planning and mentor less experienced staff on core functional technical and procedural matters as opportunities arise.Follow all key internal business practices and external regulations governing the role (e.g. GLP or GMP), and adhere to all corporate policies governing the business activities.Contributes to ongoing client updates and final reports in a timely manner and present data at client meetings.Support client projects either as an individual contributor or as a PC project leader: performing experiments, reporting results, hosting and presenting data at project meetings, delegating work, being accountable for project deliverables and demonstrating leadership behaviours. In addition, supervise multiple individual contributors and be accountable for the whole teams' deliverables on a project. Responsible for any mixed model projects and tech transfer within the Pharmaron network.What We're Looking ForPhD or equivalent in chemistry or related fieldMSc or BSc in chemistry or related fieldFor those with PhD: Evidence of strong academic or industrial achievement with at least 7-11 years' experience in such roleFor those with MSc or BSc: Evidence of strong academic or industrial achievement with at least 11-15 (MSc) or 12-16 (BSc) years' experience in such roleEvidence of strong academic or industrial laboratory experience with at least 5 years' experience in such rolesEvidence of experience in successful application of analytical / physical skill sets to resolve high complexity chemical problems such as those required within the roleEvidence of ability to effectively contribute to multi-disciplinary scientific teamsEvidence of ability to effectively supervise staffManagement of small teams (2-3 people)Why Pharmaron?Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:Comprehensive Medical, Dental & Vision Insurance with significant employer contributions401(k) Retirement Plan with generous employer matchingGenerous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balanceEmployer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability InsuranceEmployee Assistance Program (EAP), mental health resources, and wellness programsFamily-friendly benefits, including fertility support and maternity resourcesProfessional development and career growth opportunities within a leading global CRO/CDMOHow to Apply:Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.#LI-KS