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Quality Control Biotechnology Jobs (NOW HIRING)

Specialist QC

West Greenwich, RI

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Specialist QC

West Greenwich, RI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Bachelor's or Master's Degree in Biology, Immunology or a related Science field * 4 to 6 years of biotech industry experience related to Quality Control * 2 years of experience supervising or leading ...

Lead QC Microbiologist

Lexington, KY · On-site

$25.25 - $33.25/hr

Bachelor's degree in Microbiology, Biology, Biotechnology, or a related scientific discipline required. * Five or more years of QC microbiology experience in a pharmaceutical, biotechnology, medical ...

Lead QC Microbiologist

Lexington, KY · On-site

$25.25 - $33.25/hr

Bachelor's degree in Microbiology, Biology, Biotechnology, or a related scientific discipline required. * Five or more years of QC microbiology experience in a pharmaceutical, biotechnology, medical ...

QC Analyst

Novato, CA · On-site

$28 - $32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

Quality Control Manager

Bogart, GA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Microbiology experience in quality control within a biotech , pharmaceutical , or biopharmaceutical manufacturing environment is helpful. * Prior supervisory experience is preferred. Competencies

Quality Control Manager

Bogart, GA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Microbiology experience in quality control within a biotech , pharmaceutical , or biopharmaceutical manufacturing environment is helpful. * Prior supervisory experience is preferred. Competencies

QC Manager

Exton, PA · On-site

Quality Control (QC) Manager Department: Biomarker & Biologics Location: Exton, PA ( Onsite ... Bachelor's or Master's in Biology, Biochemistry, Immunology, Biotechnology, or related field.

QC Analyst

Novato, CA · On-site

$28 - $32/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Wednesday - Saturday (Onsite 4 days), swing shift (1pm-11:30 pm) Overview Leading biotechnology company looking for an experienced QC Analyst. Ideal candidates should have a bachelors degree and 0-3 ...

Quality Control Manager

Bogart, GA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Microbiology experience in quality control within a biotech , pharmaceutical , or biopharmaceutical manufacturing environment is helpful. * Prior supervisory experience is preferred. Competencies

Showing results 41-60

Quality Control Biotechnology information

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How much do quality control biotechnology jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for quality control biotechnology in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What is a quality control biotechnology job?

Quality Control Biotechnology jobs involve ensuring that biotechnological products, such as pharmaceuticals, vaccines, or laboratory reagents, meet required quality and safety standards. Professionals in this field design and perform tests, analyze data, and document results to verify that products comply with regulatory guidelines. They often work in laboratories, using specialized equipment to detect contaminants or inconsistencies. These roles are crucial for maintaining product integrity and protecting public health.

What are the key skills and qualifications needed to thrive as a quality control biotechnology professional?

To thrive as a Quality Control professional in Biotechnology, you need a solid background in biology or chemistry, attention to detail, and knowledge of regulatory standards, often supported by a relevant degree. Familiarity with laboratory equipment, analytical techniques (like HPLC, PCR), and quality management systems such as GMP or ISO 9001 is typically required. Strong problem-solving skills, teamwork, and clear communication help you excel in ensuring product integrity and compliance. These skills are crucial for maintaining high product standards, meeting regulatory requirements, and ensuring the safety and efficacy of biotechnological products.

What are typical challenges faced by professionals in quality control biotechnology, and how can they be addressed?

Professionals in Quality Control Biotechnology often encounter challenges such as maintaining compliance with stringent regulatory standards, managing tight deadlines for product release, and adapting to rapidly evolving technologies. To address these issues, staying updated on regulatory changes, implementing robust documentation practices, and participating in ongoing training are essential. Collaboration with cross-functional teams, such as Research & Development and Manufacturing, also helps ensure that quality standards are integrated throughout the production process.

What is the difference between Quality Control Biotechnology vs Quality Assurance Biotechnology?

AspectQuality Control BiotechnologyQuality Assurance Biotechnology
Primary FocusTesting and inspecting biotech products to ensure they meet standardsDeveloping and implementing processes to prevent defects and ensure quality
Work EnvironmentLaboratories, testing facilitiesOffice settings, compliance departments
CertificationsGMP, GLP, laboratory certificationsGMP, ISO, audit-related certifications

While both roles aim to ensure biotech product quality, Quality Control Biotechnology focuses on testing and inspection, whereas Quality Assurance Biotechnology emphasizes process development and compliance to prevent issues. Both are essential for product integrity in the biotech industry.

How to become a quality control biotechnology specialist?

To become a quality control biotechnology specialist, candidates typically need a bachelor's degree in biotechnology, biology, or a related field. Gaining experience with laboratory techniques, quality assurance protocols, and regulatory standards such as GMP or ISO is important, and certifications like ASQ's Certified Quality Auditor can enhance prospects. Strong attention to detail, analytical skills, and familiarity with laboratory equipment are also essential for success in this role.

What does quality control biotechnology do in biotech?

Quality Control Biotechnology professionals are responsible for testing and analyzing biological products to ensure they meet safety, quality, and regulatory standards. They perform assays, validate processes, and document results using laboratory instruments and techniques, often working under Good Manufacturing Practice (GMP) guidelines. Their work helps ensure the integrity and compliance of biotech products before they reach the market.
More about Quality Control Biotechnology jobs

What cities are hiring for Quality Control Biotechnology jobs?

Cities with the most Quality Control Biotechnology job openings:

What states have the most Quality Control Biotechnology jobs?

States with the most job openings for Quality Control Biotechnology jobs include:

Infographic showing various Quality Control Biotechnology job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Specialist QC

Amgen

West Greenwich, RI

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 7 days ago


Job description

Career CategoryOperationsJob 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.

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Salary Range

100,450.45USD -135,903.55USD