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Validation Engineer

GlaxoSmithKline
United States, Pennsylvania, King of Prussia
709 Swedeland Road (Show on map)
Jun 26, 2026
This Validation Engineer will be responsible for equipment/facility validation projects in a hands on role including writing validation protocols, scheduling and executing testing, gathering and analyzing data, and writing validation summary reports. This person will participate as a supporting member representing validation on project teams. Validation Engineers will lead specific validation projects.

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

  • Design required validation studies and write protocols for the facility and equipment.

  • Coordinate resources required to complete validation studies in a timely manner.

  • Execute validation studies per required schedules in a safe, compliant manner (e.g. LOTO).

  • Analyze test data and report questions/issues. Lead and document investigations of failed validation test results.

  • Complete validation protocols and validation summary reports with necessary approvals.

  • Support the review of new systems and modifications to existing systems to ensure designs comply with cGMPs and are able to be validated and maintained in a validated state.

  • Maintain validation equipment and supplies to enable validation to be completed per schedule requirements.

  • Support the development of required validation procedures and practices with respect to the facility.

  • Identify issues and/or improvements to validation procedures, practices, and policies related to validation, equipment and processes.

Why you? Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • Bachelor's degree in a scientific discipline

  • OR 2+ years of experience working in a regulated GMP environment with an Associated degree

  • On site role

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • 1+ years of experience in Validation, Automation or Process engineering

  • Familiar with cGMPs.

  • Strong interpersonal and organizational skills.

  • Technical understanding of the industry and validation practices related to the pharmaceutical industry is preferred.

  • Strong verbal and written communication skills.

  • Must be able to interact well with peers and senior personnel in multidisciplinary teams involving scientific, engineering, and operational disciplines.

  • Able to take directions and effective at implementing decisions.

  • Must have strong technical writing skills

#LI-GSK

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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