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Biotech Quality Control Jobs in Rhode Island (NOW HIRING)

Amgen, Inc.

Specialist QC

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ...

Amgen

Specialist QC

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ...

Amgen SA

Specialist QC

West Greenwich, RI · On-site

$95 - $125/hr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ...

New

Amgen, Inc.

QC Specialist

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... QC Specialist What you will do Let's do this. Let's change the world. In this vital role you will ...

Amgen

QC Specialist

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... QC Specialist What you will do Let's do this. Let's change the world. In this vital role you will ...

Amgen

Quality Control Associate

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ...

Posted today

Amgen

Manager QA - Nights

West Greenwich, RI · On-site

Manager QA - Nights What you will do Let's do this. Let's change the world. In this vital role you ... change control * Experience in regulations, standards and guidelines that apply to biotech ...

New

Amgen, Inc.

Manager QA - Nights

West Greenwich, RI · On-site

Manager QA - Nights What you will do Let's do this. Let's change the world. In this vital role you ... change control * Experience in regulations, standards and guidelines that apply to biotech ...

Amgen

Sr Associate QA - Nights

West Greenwich, RI · On-site

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Control, and Facilities/Engineering staff regarding compliance and quality systems.

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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 Aug 21, 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.

What is a biotech quality control?

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 does a biotech quality control do?

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.

What are the key skills and qualifications needed to thrive in biotech quality control?

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 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 August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $79,641 per year, or $38.3 per hour.

Specialist QC

Amgen, Inc.

West Greenwich, RI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago

Job description

Career Category
Operations
Job Description
Join Amgen's Mission of Serving Patients
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Specialist QC
What you will do
Let's do this. Let's change the world. In this vital role you will support analytical investigations ownership within the QC Technical Services team at Amgen.
Responsibilities:
Analytical Investigation Ownership
  • Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results.
  • Perform scientifically sound root cause analysis and develop effective corrective and preventive actions (CAPAs).
  • Ensure investigations are completed accurately, on time, and in compliance with GMP requirements and internal quality standards.

Quality Systems & Risk Assessment
  • Own and support deviations, CAPAs, and effectiveness verifications as assigned.
  • Review and approve equipment-related change controls, as applicable.
  • Partner with Quality Assurance to ensure investigation outcomes are risk-based and inspection-ready.
  • May support additional project-based assignments as required.

Cross-Functional Collaboration
  • Collaborate with Quality Control laboratories, Manufacturing, Process Development, Quality Assurance, Supply Chain, and other functional groups to resolve complex quality events.
  • Facilitate effective communication among stakeholders to ensure timely investigation progression and issue resolution.
  • Engage subject matter experts as needed to support technically complex investigations.

Inspection Readiness
  • Support internal and external audits by clearly communicating investigation findings, root cause, and CAPA effectiveness.
  • Maintain complete, accurate, and inspection-ready documentation.

What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a collaborative teammate with these qualifications.
Basic Qualifications
  • High school diploma/GED and 10 years of directly related experience OR
  • Associate's degree and 8 years of directly related experience OR
  • Bachelor's degree and 4 years of directly related experience OR
  • Master's degree and 2 years of directly related experience OR
  • Doctorate degree

Preferred Qualifications
  • Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or another Life Science discipline.
  • 5-8+ years of Quality Control or Quality Assurance experience within the biotechnology or pharmaceutical industry.
  • Demonstrated experience leading complex laboratory investigations, including OOS, OOT, atypical results, and laboratory deviations.
  • Strong knowledge of GMP regulations, laboratory quality systems, and deviation management processes.
  • Experience performing root cause analysis using structured problem-solving methodologies.
  • Strong understanding of analytical laboratory techniques, instrumentation, and data integrity principles.
  • Experience authoring and managing deviations, CAPAs, change controls, and effectiveness verifications.
  • Ability to evaluate technical data, assess risk, and make sound, science-based decisions.
  • Strong written and verbal communication skills with the ability to influence cross-functional teams.
  • Experience supporting regulatory inspections and responding to auditor inquiries.
  • Experience utilizing digital tools, data analytics, or AI-enabled technologies to improve laboratory processes is preferred.

What you can expect from us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Salary Range
100,450.45USD -135,903.55 USD

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