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Lead Process Engineer

GSK
King of Prussia, PA Full Time
POSTED ON 4/4/2025 CLOSED ON 4/25/2025

What are the responsibilities and job description for the Lead Process Engineer position at GSK?

Site Name: USA - Pennsylvania - King of Prussia

Posted Date: Apr 4 2025

Are you energized by an engineering role that enhances your leadership capabilities and allows you to shape process improvement across the site? If so, this Process Engineer role could be an exciting opportunity to explore.

The purpose of the Lead Process Engineer position is to be a technical expert and leader for the Process Engineering team within a value stream at the UM biopharm site. Team responsibilities include engineering support for the manufacture of microbial and mammalian biopharm drug substance, implementation of new processes and products into the site, project management for improvements and upgrades, and being subject matter experts for all the above.

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


  • Lead project teams as assigned to meet operational, technical, budget and schedule goals.
  • Lead in the evaluation, selection, and implementation of new equipment or modifications to existing systems with consideration to new processing technologies or strategies. This may include assessing an economic, environmental, quality, or productivity impact.
  • Use OE Tools to gather and analyze data on equipment/facility service problems in order to identify the root cause of the problem and generate possible solutions to equipment/facility service problems based upon the facts gathered.
  • Lead discussions and recommend solutions with key customer groups in order to gain a consensus on the repair or modification plans.
  • Develop a project plan and budget, and then implement the approved modifications, following up to ensure the desired result has been achieved. Document modifications in an appropriate manner.
  • Provide training to staff involved in the use or maintenance of equipment to ensure safe and reliable operation.
  • Prepare or review operation, safety and maintenance procedures to ensure accuracy and completeness.
  • Support validation staff in the development of validation strategies and testing plans; assess and recommend solutions for validation protocol deviations.
  • Provide operational support to production and automation in a proactive hands-on manner. Mentor and assist in skills development of the process engineers within the department. Provide real-time and in-person process monitoring and technical oversight for a 24-7 manufacturing facility which will require off hours and weekend support as needed
  • Delegate project duties within the department or value stream team and understand the execution of those duties.


Why you?

Basic Qualifications:

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


  • BS or BA in engineering
  • 3 years’ experience in pharma/biopharma manufacturing
  • 2 years’ experience as a process engineer
  • 1 years’ experience with cGMP (current Good Manufacturing Practices)


Preferred Qualifications:

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


  • Prior project experience in the design, construction, start-up and operation of large bulk biopharmaceutical facilities including cell culture and/or microbial fermentation, or protein recovery and purification.
  • Demonstrated ability to manage projects to completion on time and within budget.
  • Knowledgeable in cGMP’s and NIH guideline for large scale recombinant biological processing.
  • Strong technical understanding of the pharmaceutical industry and engineering practices.
  • Must be able to interact well with peers, subordinates, and senior personnel in scientific, engineering, and operational disciplines.
  • Demonstrated ability to participate as a leader or member on cross-functional and self-directed work teams
  • Strong communication skills are imperative


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 1 801 567 5155 (outside US).

GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

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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