Lead the Manufacturing Science & Technology organization at the Halle radiopharmaceutical production site, driving process robustness, validation, and technical excellence.
Compensation
Expected Annual Base Salary Range for role: € 97,900 to € 146,900
Responsibilities
Set strategic direction for Manufacturing Science & Technology
Serve as key partner for site and platform leadership
Strengthen knowledge management and technical standards
Ensure robust product stewardship and oversight
Drive manufacturing process robustness and continuous improvement
Requirements
Master’s degree in Chemistry, Pharmacy, Chemical Engineering, Pharmaceutical Technology, or related scientific discipline
Process Engineer in Product Development Science & Technology supporting API projects through late-stage development, commercialization, and manufacturing.
Responsibilities
Leverage core chemical engineering principles in experimental design and data analysis
Ensure processes can be run safely and address scale-up issues
Develop and implement robust API process steps from lab to manufacturing
Lead research and project activities within cross-functional teams
Communicate findings in multidisciplinary teams
Requirements
BS, MS, or PhD in chemical engineering or a related field
The ASTL is responsible for the leadership and delivery of business-critical projects to support all analytical aspects related to the late phase of the product lifecycle for key GSK products, including managing comparability studies and characterization strategies for post-approval changes.
Locations (2)
Ware, Hertfordshire, United Kingdom
Upper Merion, Pennsylvania, United States
Responsibilities
Provide technical analytical leadership for programs, projects, and activities related to the specific product/s under the ASTL accountability to ensure business priorities and targets are met (NPI, product transfers, change management, regulatory submissions).
Be accountable for the Analytical Product strategy (APS); maintenance and update of the APS through the post-approval product lifecycle, recommending specification and stability strategies, and novel analytical technologies.
Manage and define comparability studies and suitable characterization strategies to support post-approval changes.
Compile and recommend acceptance criteria for release and stability tests to feed into comparability strategies around TT process, change scale, and material change.
Lead technical oversight and process improvement for global pharmaceutical packaging operations, ensuring reliable supply and regulatory compliance across multiple sites.
Compensation
$67,500 - $173,800
Responsibilities
Provide technical oversight for commercial medicines packaging
Support technical transfer and implementation of new packaging lines
Develop and implement risk management and control strategies
Coordinate with global functions and site SMEs
Travel to packaging sites for on‑ground support
Requirements
Degree in Packaging/Mechanical/Chemical Engineering or related engineering/scientific discipline
Nice to have: Device and parenteral product development
Lead and manage engineering scheduling for capital projects across the GES portfolio, coaching teams, developing schedules, and ensuring compliance with industry standards.
Locations (3)
Rahway, New Jersey, United States
San Francisco, California, United States
Los Angeles, California, United States
Compensation
The salary range for the primary location of this role is: $142,400.00 - $224,100.00
Responsibilities
Support a portfolio of Capital Projects, responsible for the conceptualization and development of front end loaded schedules that support critical business objectives primarily at US Sites.
Provide expertise to business studies, peer reviews of projects, and periodic improvement initiatives to advance standard work processes within GES.
Associate Director, Engineering, GES Strategic Scheduler and Planner
Lead and collaborate with integrated capital project teams to develop and execute strategic schedules for pharmaceutical manufacturing projects.
Compensation
$142,400.00 - $224,100.00
Responsibilities
Support a portfolio of Capital Projects, responsible for the conceptualization and development of front end loaded schedules that support critical business objectives primarily at US Sites.
Provide expertise to business studies, peer reviews of projects, and periodic improvement initiatives to advance standard work processes within GES.
Lead and collaborate with other Integrated Capital Project Team members, including GES Tech Center, Delivery, End-to-End Solutions and Project Business Service (PBS) Engineers, Internal Organization Capital Team Leaders, Digital, Site Engineering, Operations, Quality, Validation and Regulatory Representatives, External Contractors, Equipment Vendors, and Service Providers.
Evaluate and challenge the work of engineering partners in the preparation of project related deliverables across many diverse areas including Biological, Chemical, Safety, Process, Utilities, Technical Services, Construction, Procurement, Commissioning & Qualification, and Validation.
Facilitate planning sessions and guide team members through a planning strategy.
Lead synthetic molecule route development and unit operation definition for preclinical to Phase 2 studies, overseeing cross‑disciplinary teams and external R&D collaborations.
Compensation
$153,000 - $264,000
Responsibilities
Demonstrate expertise in modern synthetic organic and process chemistry
Lead design and development of new synthetic routes for API
Design experimental laboratory plans for route and process optimization
Lead cross‑disciplinary teams to evaluate and refine manufacturing routes
Collaborate in technology transfer activities to CRO/CMO and internal manufacturing nodes
The Technical Services and Manufacturing Sciences (TSMS) Technical Transfer Engineer will be responsible for supporting all facets of Tech transfer, Process Validation, GMP Floor Support, and Continued Process Verification in accordance with current good manufacturing (cGMP) for clinical and commercial programs.
Responsibilities
Autonomously scale up and transfer process into full scale manufacturing process based on data generated internally or received from the client
Select appropriate equipment and single-use components for GMP manufacturing and develop technical documentation such as Tech Transfer Plan, Gap Assessment, Process Flow Diagram, Summary Reports and Process FMEA
Represent TSMS in project teams and communicate directly with customers
Recognized as Subject Matter Expert for the manufacturing processes
Author GMP manufacturing documentation including Master Batch Records, Bill of Materials and Processing Forms
Requirements
Bachelors’ degree in Science or Engineering
Masters’ degree in Science or Engineering preferred
Provide analytical input and expertise into comparability protocols and reports, taking into account non-routine physical properties data and recommendations from Materials Science.
Lead and collaborate with other Integrated Capital Project Team members, including GES Tech Center, Delivery, End-to-End Solutions and Project Business Service (PBS) Engineers, Internal Organization Capital Team Leaders, Digital, Site Engineering, Operations, Quality, Validation and Regulatory Representatives, External Contractors, Equipment Vendors, and Service Providers.
Evaluate and challenge the work of engineering partners in the preparation of project related deliverables across many diverse areas including Biological, Chemical, Safety, Process, Utilities, Technical Services, Construction, Procurement, Commissioning & Qualification, and Validation.
Facilitate planning sessions and guide team members through a planning strategy.
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