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Biopharmaceutical Microbiologist Jobs (NOW HIRING)

Senior QC Microbiologist

Holly Springs, NC · On-site

$22 - $29/hr

Position Overview The Senior, QC Microbiology supports t QC, detecting, and mitigating microbial ... By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ...

Senior QC Microbiologist

Holly Springs, NC · On-site

$22 - $29/hr

Position Overview The Senior, QC Microbiology supports t QC, detecting, and mitigating microbial ... By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ...

Senior QC Microbiologist

Holly Springs, NC · On-site

$22 - $29/hr

The Senior, QC Microbiology supports t QC, detecting, and mitigating microbial contamination across ... By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ...

$22 - $29/hr

Position OverviewThe Senior, QC Microbiology supports t QC, detecting, and mitigating microbial ... By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ...

R&D Partners is seeking to hire a Quality Control Microbiology Tech in Frederick, MD . Your main ... We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and ...

Showing results 21-40

Biopharmaceutical Microbiologist information

See salary details

$34.5K

$70.6K

$126K

How much do biopharmaceutical microbiologist jobs pay per year?

As of Aug 12, 2026, the average yearly pay for biopharmaceutical microbiologist in the United States is $70,647.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,500.00 and $83,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a biopharmaceutical microbiologist?

To thrive as a Biopharmaceutical Microbiologist, you need a strong background in microbiology, biochemistry, and aseptic techniques, typically supported by a degree in microbiology or related life sciences. Familiarity with laboratory information management systems (LIMS), GMP/GLP regulations, and microbial identification tools is essential. Attention to detail, analytical thinking, and effective communication are key soft skills that distinguish top performers in this field. These competencies ensure accurate contamination control, regulatory compliance, and the safe development of biopharmaceutical products.

What is a biopharmaceutical microbiologist?

Biopharmaceutical microbiologists are scientists who study microorganisms, such as bacteria, fungi, and viruses, in the context of developing and manufacturing pharmaceuticals derived from biological sources. They play a key role in ensuring the safety, efficacy, and quality of biopharmaceutical products by monitoring microbial contamination, optimizing production processes, and complying with regulatory standards. Their work is crucial in the research, development, and production of vaccines, therapeutic proteins, and other biologic drugs.

What is the difference between Biopharmaceutical Microbiologist vs Pharmaceutical Microbiologist?

AspectBiopharmaceutical MicrobiologistPharmaceutical Microbiologist
CredentialsBachelor's or Master's in Microbiology, Biotechnology, or related field; certifications like ASM Microbiology CertificationBachelor's or Master's in Microbiology, Pharmaceutical Sciences, or related; similar certifications
Work EnvironmentLaboratories focused on biologics, vaccines, and biopharmaceutical productsLabs working on various pharmaceutical products, including drugs and vaccines
Industry UsagePrimarily in biotech and biopharmaceutical companiesIn both pharmaceutical manufacturing and research sectors

Both roles require similar educational backgrounds and certifications, often working in laboratory settings. The main difference lies in their focus: biopharmaceutical microbiologists specialize in biologics and vaccines, while pharmaceutical microbiologists work across a broader range of drug products. Understanding these distinctions helps job seekers target the right roles in the industry.

What are some common challenges faced by biopharmaceutical microbiologists in ensuring product safety and quality?

Biopharmaceutical microbiologists often encounter challenges related to maintaining sterile environments and preventing contamination during the manufacturing process. They must adhere to strict regulatory standards and regularly conduct quality control tests, such as environmental monitoring and microbial limit testing. Collaboration with cross-functional teams, such as manufacturing and quality assurance, is essential to quickly address any deviations or contamination events. Staying up-to-date with evolving regulatory guidelines and advancements in rapid microbiological methods is also crucial for success in this role.
More about Biopharmaceutical Microbiologist jobs
Infographic showing various Biopharmaceutical Microbiologist job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 1% Part Time, 1% Temporary, and 4% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $70,647 per year, or $34 per hour.

Scientist, Microbiology and Sterility Assurance

GSK

King Of Prussia, PA • On-site

Full-time

Posted 7 days ago


GlaxoSmithKline rating

8.9

Company rating: 8.9 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

9th of 86 rated pharmaceutical


Job description

Business Introduction
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. We're uniting science, technology, and talent to get ahead of disease together.
Find out more:
Our approach to R&D
This position will initially be located at the GSK's Upper Merion site in Upper Merion, Pennsylvania from 2026 to 2027/2028, and will permanently move to Marietta, Pennsylvania afterwards.
Position Summary
You will join a team that ensures medicines reach patients safely. In this scientist role you will lead microbiology and sterility assurance activities for a sterile R&D manufacturing facility. You will work closely with manufacturing, quality, and development teams to prevent contamination and support product release. We value practical laboratory skills, clear communication, and a mindset for continuous improvement. This role offers growth, a chance to make a measurable impact on patient safety, and alignment with GSK's mission to unite science, technology and talent to get ahead of disease together.
Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
  • Provide hands-on microbiology support for sterile operations, including aseptic processing, environmental monitoring, and gowning qualifications.

  • Lead investigations of unexpected microbiological results and drive corrective actions with clear root cause and risk assessment.

  • Perform and review routine microbiological testing: bioburden, sterility, endotoxin, microbial identifications, and water testing.

  • Develop, revise, and approve microbiological methods, SOPs, and sampling plans that support product release and stability programs.

  • Partner with manufacturing, quality, and development teams to define and implement contamination control and sterility assurance strategies.

  • Support validation activities, method transfers, and evaluation of rapid microbiological technologies.

Why You?
Work model
This role requires being on site 5 days per week for laboratory and sterile-facility responsibilities. Candidates must be able to be on site as required to meet operational needs.
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals
  • Bachelor's degree in Microbiology, Biology, Biotechnology, or a related scientific discipline.

  • Minimum 3 years' hands-on experience in a pharmaceutical, biotech, or sterile manufacturing microbiology laboratory.

  • Experience with environmental monitoring, aseptic techniques, gowning, and contamination control.

  • cGMP principles and experience working to regulatory quality standards.

  • Experience performing bioburden, sterility, endotoxin testing, and microbial identifications.

Preferred Qualification
If you have the following characteristics, it would be a plus
  • Advanced degree (Master's) in Microbiology or related field.

  • Experience with method development, validation, or transfers for microbiological assays.

  • Familiarity with pharmacopeial microbiology standards and compendial methods.

  • Experience using laboratory information management systems (LIMS) and electronic documentation.

  • Prior experience reviewing microbiology data for regulatory submissions or CMC support.

  • Demonstrated ability to lead technical investigations and communicate findings clearly to stakeholders.

#GSK-LI
What we value
We look for people who work with pace and good judgement. You will deliver high-quality results and learn continuously. You will collaborate openly and support team wellbeing. We expect accountability, clear communication, and a focus on patient safety.
Apply now
If this role fits your skills and ambitions, we encourage you to apply. We welcome applicants from all backgrounds and perspectives. Join us to help get ahead of disease together.
Skills
Bacteriology, Drug Discovery Process, Laboratory Operations, Laboratory Quality Control, Microbiology, Pharmaceutical Manufacturing, Project Management, Regulatory Filings
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

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About GlaxoSmithKline

Sourced by ZipRecruiter

GlaxoSmithKline is a globally recognized pharmaceutical and healthcare company based in Philadelphia, PA, USA. Originated from a merger between Glaxo Wellcome and SmithKline Beecham in 2000, the company excels in the pharmaceutical industry and holds a leading position in making medicines, vaccines, and consumer healthcare products. GSK's mission is to improve the quality of human life by enabling people to do more, feel better, and live longer. They adhere to core values of transparency, integrity, respect for people, and patient-focus, reflecting in their endeavors to conduct research and deliver innovative healthcare solutions to patients and consumers worldwide.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Philadelphia, PA, US