Project Engineer
Quick Summary
Lead and/or participate in the design and installation of new, or modifications to existing, process and/or utility systems, including bioreactors, chromatography skids, depth filtration skids,
This role will manage up to $2m of capital across multiple projects involving commercial-scale process equipment and manufacturing suites. Responsibilities are inclusive of project management, design, installation, qualification, and improvement of equipment and facilities in an EHS- / Regulatory- / GEP-compliant manner at the Upper Merion GSC Biopharm site.
Responsibilities
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 and/or utility systems, including bioreactors, chromatography skids, depth filtration skids, UFDF skids, etc., to meet technical, budget, and schedule goals.
- Demonstrate good project management skills (schedule, cost, communications) and coordinate outside and internal resources to safely execute projects in a timely and cost-effective manner.
- Ensure projects are completed in compliance with applicable standards, policies, and regulations (Engineering Standards, GSK policies, cGMP, Project Management Framework (PMF) and other regulatory requirements).
- Lead discussions and recommend solutions with key customer groups in order to gain a consensus on project scope and execution plan.
- Be personally responsible for the coordination of all Engineering activities from implementation to handover to customer for a given project, including management of third party engineering firms and/or trades.
- In cooperation with the Validation Group, develop commissioning and validation documentation, including test protocols, and implement validation plans on new process and utility systems and changes to existing systems, in order to maintain the validated status of existing systems.
- Stay current with developments in the field of biopharm technology. Support the transfer of technology from development into manufacturing.
- Follow up on projects’ status and arising issues/changes with all relevant parties (customer, finance, procurement and engineering departments).
- Be fluent in site safety procedures (LOTO, PTW, etc) and engineering standards to deliver projects aligned with EHS and engineering compliance requirements. Apply corporate EHS standards related to employee’s safety during construction/ demolition processes to achieve zero reportable injury rate, with continuous supervision and control on contractors’ activities.
Requirements
~1 min read
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
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.
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Location & Eligibility
Listing Details
- Posted
- October 9, 2026
- First seen
- October 9, 2026
- Last seen
- October 9, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 56%
- Scored at
- October 9, 2026
Signal breakdown
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