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Scientist, Microbiology and Sterility Assurance

GSK


Job Location:

Marietta, GA - USA

Monthly Salary: Not provided by the employer
Posted: 7 August 2026 (28 days ago)
Application Deadline: 15 November 2026
Vacancies: 1 Vacancy

Job Summary

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 peoples 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. Were uniting science technology and talent to get ahead of disease together.


Find out more:
Our approach to R&D

This position will initially belocatedat the GSKs 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 thisscientistroleyou 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 GSKs mission to unite sciencetechnologyand 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.

  • Supportvalidationactivities 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

  • Bachelors degree in Microbiology Biology Biotechnology ora relatedscientific 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 microbialidentifications.


Preferred Qualification


If you have the following characteristics it would be a plus

  • Advanced degree (Masters) 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



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 were 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 -

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 GSKs 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 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 GSKs compliance to all federal and state US Transparency requirements. For more information please visit the Centers for Medicare and Medicaid Services (CMS) website at Experience:

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About Company

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About us We are a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We have 3 global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.

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