GSK · 1 day ago
Process Engineer
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. The Process Engineer at the Rockville Biopharm site will provide technical engineering and project management services for cGMP manufacturing operations, focusing on equipment optimization and technology transfer support.
BiotechnologyHealthcarePharmaceuticalHealth Care
Responsibilities
Provide engineering support for the design, testing and optimization of biopharmaceutical manufacturing equipment up to 20,000L scale including stainless and single-use bioreactors, centrifuges, chromatography systems, filtration skids, pasteurizers, chromatography skids, etc
Manage capital projects and engineer solutions involving retrofits, modifications and acquisition of process equipment
Support execution of technology transfer and scale-up activities
Lead resolution of technical issues with manufacturing operations and equipment
Collaborates with other manufacturing support groups including Validation, Automation, Quality, Metrology, Maintenance and Process Development
Applies knowledge of process and utility systems to make recommendations to improve manufacturing systems, equipment and process efficiencies
Experience with project management (schedule, cost, communications) and coordination of internal and external resources to execute projects in a timely and cost-effective manner
Subject matter expert (SME) and equipment owner for Upstream and/or Downstream process equipment with ability to assist in the execution of design, procurement, testing (FAT, SAT, commissioning), installation and validation activities
Capable of negotiating contracts, bids, and change orders with vendors or contractors
Support investigations and recommend solutions with key stakeholders in order to gain a consensus on effective corrective and preventive actions (CAPA)
Qualification
Required
BS in Engineering or related technical discipline such as Biological, Chemical, Mechanical
2+ years of experience working in a regulated cGMP biopharmaceutical environment
Preferred
Experience with technical risk assessments and product control strategies
Capable of working in a collaborative and team focused environment
Demonstrated understanding of the product development process
Able to evaluate potential innovative technology areas relevant to products
Experience supporting batch and continuous industrial control systems
Change control and deviation management experience
Must be proficient with common business enterprise technologies including MS Office
Working knowledge of biopharmaceutical production, quality systems and clinical or commercial manufacturing including cell culture and/or microbial processes
Demonstrated ability to participate as a member of a cross-functional team
Basic understanding and knowledge of biopharmaceutical production equipment including but not limited to bioreactors, centrifuges, CIP skids, chromatography systems and filtration skids
Project management experience, including the ability to manage a project by delivering scope, cost and schedule
Benefits
Health care and other insurance benefits (for employee and family)
Retirement benefits
Paid holidays
Vacation
Paid caregiver/parental and medical leave
Company
GSK
We are uniting science, technology and talent to get ahead of disease together. Our community guidelines: https://gsk.to/socialmedia
H1B Sponsorship
GSK has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (45)
2024 (56)
2023 (54)
2022 (53)
2021 (54)
2020 (72)
Funding
Current Stage
Public CompanyTotal Funding
$25.51MKey Investors
CARB-X
2021-03-02Grant· $18M
2020-09-23Grant· $7.51M
1978-01-13IPO
Recent News
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2026-02-03
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