# Molecule Steward **Company**: GSK **Location**: Pennsylvania - Upper Providence **Experience**: senior **Job type**: full-time **Category**: Logistics & Supply Chain **Industry**: Healthcare **Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Upper-Providence/Molecule-Steward_451373-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply **Canonical**: https://yubhub.co/job/molecule-steward-965962f6-d76/ ## Description We are seeking an experienced scientific professional to take end-to-end technical accountability for a given product, from bulk API manufacturing, formulation, packing and related support activities, providing strategic technical leadership to ensure successful new product introduction, quality robustness and productivity improvements across the lifecycle. The Molecule Steward is aligned to a new asset at Commit to Commercial Development with responsibility for representing MSAT in the development of the Product Control Strategy. When the product transfers to GSC accountability, the Molecule Steward co-ordinates Drug Substance, Drug Product, Analytical Strategy and, if appropriate, Device Leads to maintain the Product Control Strategy and ensure the product is maintained in the desired state of control throughout product lifecycle. **Responsibilities** - Representing MSAT as technical single-point accountable decision maker to CMC Matrix and Medicine Supply Chain teams, ensuring that a product control strategy is defined and maintained to drive a robust product that meets target manufacturability criteria. - Responsible for defining the End-to-End Product Performance Qualification and Ongoing Continuous Verification Strategy for the product, including trending and sampling plans and ensuring alignment and consistency across supply nodes. - Maintaining accountability for the product, from transfer from R&D throughout its lifecycle, ensuring improvement plans (including 2nd generation processes) are developed and delivered impacting the manufacturing process, analytical process, pack, device, and associated specifications to deliver value. - Maintaining solid knowledge and understanding of complex scientific subject matter as well as evolving regulatory policies and guidelines and industry best practices. This knowledge is used in developing improvement plans for the products. - Accountable from an MSAT perspective for defining technology strategy & specific solutions as required to support the overall product or dose form lifecycle. - Responsible for leading Product Technical Lifecycle Teams, ensuring risks are identified and mitigated and technical issues are resolved in a timely manner. - Responsible for co-ordinating the review of regulatory submissions and responses to technical questions within MSAT, ensuring review by appropriate SMEs and sites. - Providing leadership and subject matter expertise where required for investigations and/or critical deviations, troubleshooting, and major change programmes. - Ensuring that product history and knowledge from development through lifecycle is maintained and aligns with knowledge management standards for the product or dose form within the GSC network. - Managing strong collaborations with technical staff across the Supply Chain sites, MSAT & R&D, with effective and clear communication on highly technical topics. Must be able to lead and operate in an environment with high degree of change and uncertainty. **Basic Qualifications** - University Degree (minimum) in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar area - Seven or more years’ experience in small molecule pharmaceutical development and/or manufacturing - Five or more years of experience implementing regulatory requirements (MHRA, FDA), and internal/external quality and safety requirements - Five or more years of experience in technology transfer, with an understanding of the product development process - Two or more years of experience implementing current and emerging Regulatory Strategies (Quality by Design, GMP for 21st century, ICH, Q7, Q8, Q9, Q10) and Product Lifecycle Management - Five or more years of experience in the pharmaceutical industry in leading the technical aspects of Product Lifecycle Management, including supporting process investigations. **Preferred Qualifications** - Project management and prioritization skills gained within a complex matrix - Excellent problem solver and ability to think and work creatively - Strong technical acumen and communication skills with the ability to articulate complex, technical details to stakeholders and enable cross functional collaboration across sites, supply chain, R&D and suppliers - Experience managing external partners/CDMO’s in NPI and/or commercial supply - Ability to effectively influence stakeholders at all levels For more fresh new jobs, check out [yubhub.co](https://yubhub.co/). ## Skills ### Required - CMC Strategy - Data-Driven Decision Making - Data Integrity - GxP Regulations - Lean Management - Problem Solving - Process Optimization - Project Leadership - Risk Awareness - Scientific Writing - Technology Transfer ### Nice to have - Project management and prioritization skills - Excellent problem solver and ability to think and work creatively - Strong technical acumen and communication skills - Experience managing external partners/CDMO’s in NPI and/or commercial supply - Ability to effectively influence stakeholders at all levels --- Source: [Apply at gsk.wd5.myworkdayjobs.com](https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Upper-Providence/Molecule-Steward_451373-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)