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Biotech Quality Control Jobs in Rhode Island (NOW HIRING)

Pharmaron

Senior Scientist I, QC

Coventry, RI · On-site

$100K - $140K/yr

Senior Scientist I, QC Salary Range: $100,000-$130,000 Location: Coventry, RI About Pharmaron ... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ...

Pharmaron

Senior Scientist I, QC

Coventry, RI

$100K - $130K/yr

Senior Scientist I, QC Salary Range: $100,000-$130,000 Location: Coventry, RI About Pharmaron ... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ...

Pharmaron

Senior Scientist I, QC (3rd shift)

Coventry, RI · On-site

$100K - $140K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Mentor junior QC scientists on daily work, provide technical and compliance guidance. * Conduct ...

Pharmaron

Scientist II, Analytical Chemistry

Coventry, RI · On-site

$75K - $95K/yr

... biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 ... Sample raw materials and conduct QC testing of raw materials, intermediates, API, IPC and cleaning ...

Amgen

Sr Specialist QA - Compliance

West Greenwich, RI

$89K - $123K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Thorough understanding of quality management systems and quality control processes related to bulk ...

Amgen

Mgr Manufacturing - Nights

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... The Front-Line Manager will collaborate routinely with Quality Assurance, Quality Control ...

Amgen, Inc.

Sr Specialist QA - Compliance

West Greenwich, RI · On-site

$89K - $123K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Thorough understanding of quality management systems and quality control processes related to bulk ...

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All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Rhode Island

Biotech Quality Control information

See Rhode Island salary details

$29.9K

$79.6K

$126.8K

How much do biotech quality control jobs pay per year?

As of Jul 31, 2026, the average yearly pay for biotech quality control in Rhode Island is $79,641.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,200.00 and $97,900.00 per year, depending on experience, location, and employer.

Does QA or QC pay more?

In biotech quality control, Quality Assurance (QA) roles typically pay slightly more than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. Both roles require attention to detail and knowledge of industry regulations, but QA positions often involve more strategic planning and documentation, which can influence salary differences.

What are the typical daily responsibilities of someone working in Biotech Quality Control?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

How to become a biotech quality control specialist?

To become a biotech quality control specialist, candidates typically need a bachelor's degree in biology, chemistry, or a related field. Relevant skills include knowledge of laboratory techniques, quality assurance processes, and familiarity with regulatory standards like GMP. Certifications such as ASQ CQE or training in laboratory management can enhance job prospects.

What is the highest paying job in biotech?

In biotech quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

What is a Biotech Quality Control job?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in the Biotech Quality Control position, and why are they important?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What does quality control do in biotech?

In biotech, quality control (QC) involves testing and inspecting products, raw materials, and processes to ensure they meet safety, efficacy, and quality standards. QC teams use analytical techniques and documentation to identify deviations and maintain compliance with regulatory requirements such as GMP. This role is essential for ensuring product consistency and regulatory approval.
What are the most commonly searched types of Biotech Quality Control jobs in Rhode Island? The most popular types of Biotech Quality Control jobs in Rhode Island are:
What are popular job titles related to Biotech Quality Control jobs in Rhode Island? For Biotech Quality Control jobs in Rhode Island, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in Rhode Island look for? The top searched job categories for Biotech Quality Control jobs in Rhode Island are:
What cities in Rhode Island are hiring for Biotech Quality Control jobs? Cities in Rhode Island with the most Biotech Quality Control job openings:
Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Rhode Island as of July 2026, with employment types broken down into 85% Full Time, 8% Part Time, 1% Temporary, and 6% Contract. Highlights an 81% Physical, 3% Hybrid, and 16% Remote job distribution, with an average salary of $79,641 per year, or $38.3 per hour.

Senior Scientist I, QC

Pharmaron

Coventry, RI • On-site

$100K - $140K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 19 days ago

Job description

Position: Senior Scientist I, QC
Salary Range: $100,000-$130,000
Location: Coventry, RI
About Pharmaron
Pharmaron 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 .
Job Overview:
The Senior Scientist, QC supports technology transfer and GMP manufacturing activities through analytical method transfer, verification, validation, sample testing and stability study management in compliance with all applicable guidelines. Will also solve moderate complexity analytical and quality control issues for assigned projects and/or initiatives.
Key Responsibilities
  • Participate in method transfer activities, including writing method transfer and method validation protocols, executing experiments and writing reports.
  • Mentor junior QC scientists on daily work, provide technical and compliance guidance.
  • Conduct method validation, method verification and sample testing.
  • Review experimental data, notebooks, method, protocols / reports.
  • Manage stability studies, draft stability protocols and report, coordinate and perform sample testing.
  • Actively participate in investigation of laboratory deviations, OOS, OOT, and atypical results. Write investigation reports.
  • Prepare and present data summaries (written and oral) as necessary. Present to cross functional teams and effectively communicate critical QC/analytical issues and solutions.
  • Ability to work successfully in both a team/matrix environment as well as independently.
  • Ensure high quality in QC work and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.
  • Participate, support and facilitate site audits as directed and required.
  • SME for instrument and training.
  • Maintain good laboratory practices and GMP in compliance with safety and environmental requirements.
  • Write, revise, develop, and evaluate SOPs.
  • Perform other related assignments and duties, as required and assigned.

What We're Looking For
  • MS with 8+ years of experience or BS with 10 years of experience in pharmaceutical industry
  • Evidence of experience in successful application of analytical skill sets to resolve scientific problems related to method optimization and/or implementation.
  • Experienced troubleshooter of technical problems
  • 3 years of experience (may include Ph.D. experience) with core analytical instrumentation such as HPLC, GC, FTIR, Mass Spectrometry.
  • Evidence of ability to effectively contribute to multi-disciplinary scientific teams
  • Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance
  • Evidence of ability to effectively scientifically supervise staff
  • Expert application of core laboratory techniques and instrumentation to impact API, intermediates and starting materials

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 21,000 employees and operations in the U.S., the U.K. and China. 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:
  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How 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.
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