Process Engineer

GSK; King of Prussia (Montgomery County); On-site; USD 100,000 - 127,000; Full time

Job summary

A leading biopharma company seeks a Process Engineer to join their team in King of Prussia. The role involves designing and maintaining process systems, troubleshooting issues, and providing support for production activities, emphasizing a hands-on approach and collaboration across teams.

Qualifications

• 1+ year prior process engineering experience in the pharmaceutical industry.
• Familiarity with P&ID’s and plant operations.

Responsibilities

• Lead and participate in design and installation of process systems.
• Provide operational support for production and automation.
• Develop training programs on process systems.

Skills

Process Engineering

Troubleshooting

Communication

Education

BS/BA in engineering or equivalent technical discipline

Job description

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Site Name: USA - Pennsylvania - King of Prussia

Posted Date: Jun 18 2025

As a Process Engineer, you will be a technical hands-on resource for the design, installation, qualification, operation, maintenance, and improvement of equipment and facilities located at the Upper Merion PSC BioPharma site as well as support for products manufactured at third party manufacturing sites.

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

• Lead and/or participate in the design and installation of new, or modifications to existing, process or utility systems including upstream protein production systems (rocker bioreactors, bioreactors, centrifugation), downstream protein purification systems (chromatography, IDF, Viral Filtration, TFF), or utility systems to meet technical, budget, and schedule goals. Document modifications according to approved local procedures.
• Develop or review operation, safety and maintenance procedures for mechanical process and utility systems. Provide operational support to production and automation in a proactive hands-on manner.
• Troubleshoot and correct problems with process and utility systems using OE Tools and procedures.
• Provide maintenance support for existing process and utility systems. Analyze repairs and maintenance requirements to proactively address system weaknesses.
• In cooperation with the Validation Group, develop validation documentation including test protocols, and implement validation plans on new process and utility systems and changes to existing systems to maintain the validated status of existing systems.
• Develop training programs and provide training on process systems.
• Makes recommendations for improving existing systems that will reduce cost and improve system reliability.
• Stay current with developments in the field of BioPharma technology. Support the transfer of technology from development into manufacturing.
• Actively participate in the value stream team environment to ensure appropriate engineering input and integration of local and corporate engineering specifications
  
  
  

Why you?

Basic Qualifications:

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

• BS/BA in engineering or equivalent technical discipline such as a life science degree (chemical engineering preferred)
• 1+ year with prior process engineering experience in the pharmaceutical industry
• Familiarity with P&ID’s, equipment specifications, and plant operations
  
  
  

Preferred Qualifications:

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

• Familiar with cGMP’s and NIH Recombinant Guidelines for large scale biological processing.
• Understanding of pharmaceutical industry and engineering practices.
• Strong interpersonal skills.
• Must be able to work within a multi-disciplinary team environment.
• Must be able to generate options to resolve problems, prioritize solutions and implement decisions.
• Strong communication skills with the ability to effectively engage and collaborate with stakeholders across functions.
• Project Lead, Project Management experience
  
  
  

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 special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or [phone] (outside US).

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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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/

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Industries

  Pharmaceutical Manufacturing

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