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Analytical Operations Scientist

GlaxoSmithKline
United States, Pennsylvania, King of Prussia
709 Swedeland Road (Show on map)
Apr 15, 2026
Site Name: USA - Pennsylvania - King of Prussia
Posted Date: Apr 15 2026

At GSK, we are ambitious for patients. As the healthcare landscape continues to evolve-bringing new stakeholders, data sources, and expectations-we are committed to ensuring that the patient voice meaningfully informs how medicines are developed, evaluated, launched, and delivered to patients. This includes patient engagement across drug development, regulatory decisionmaking, health technology assessment, launch planning, and patient care.

This role is responsible for the manufacture of biopharmaceutical analytical reference materials and supports the R&D biopharmaceutical critical reagents program in line with regulatory and business requirements.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Manage the manufacture of analytical reference materials using automated and manual filling instrumentation.
  • Collaborate with GSK R&D and GSC analytical groups to manage manufacturing details and scheduling for reference material and reagent fills.
  • Record and archive manufacturing details to comply with GSK and regulatory requirements.
  • Maintain instrument and inventory of materials required to perform filling operations.
  • Contribute to GSK's overall critical reagent strategy for biopharmaceutical projects.
  • Shipping and receiving biopharmaceutical critical reagents and RM to support R&D, commercial, and contract testing labs.
  • Actively prepare and support internal quality and external regulatory inspections.
  • Support DDS Leadership by actively participating in the activities and initiatives that promote an organizational culture aligned with GSK Values and Expectations.
  • Adopt data and digital tools to drive continuous improvement and deliver simplified, efficient business processes.
  • Support large molecule stability team with stability protocol and data management, as needed.

Why YOU?

Basic Qualifications:

  • Bachelor of Science in Chemistry, Biology, or a related scientific discipline and 2+ years of experience in a directly related discipline.
  • 2+ years of experience in a project team or directly related discipline

Preferred Qualifications:

  • Experience in operation of automated liquid systems, e.g. Hamilton.
  • Awareness of protein stability and assays used for detection such as CGE, cIEF, HPLC, and functional assays.
  • Awareness of cGMP and Regulatory requirements for the development and commercialization of Biopharmaceuticals.
  • Excellent written and verbal communication skills.
  • Excellent organization skills and ability to handle multiple priorities.

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.

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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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