Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead a team of Molecule Stewards in innovative drug development and lifecycle management.
- Company: Join a leading pharmaceutical company dedicated to improving global health.
- Benefits: Competitive salary, annual bonus, health insurance, retirement benefits, and flexible working options.
- Other info: Hybrid work model with opportunities for career growth and mentorship.
- Why this job: Make a real impact on patient health through cutting-edge medicines and vaccines.
- Qualifications: Bachelor's degree in life sciences; experience in biopharmaceutical development preferred.
We manufacture and supply reliable, high‑quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it is vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
The Sr Director - Molecule Steward Lead will lead a group (5-15) of Molecule Stewards who have end‑to‑end technical accountability for a portfolio of innovative programs, including Drug Substance, Drug Product, inspection, assembly, packing and related support activities, providing strategic technical leadership to ensure successful new product introduction, launch, and improvements across the lifecycle (e.g. quality, robustness and productivity). The Senior Director‑Molecule Steward Lead will drive program alignment across a portfolio of assets from Commit to Commercial Design through Product sunset.
The team will represent MSAT in a variety of product lifecycle milestones including, but not limited to: development of the Product Control Strategy, Technology Transfer, PPQ and ongoing maintenance of the Control Strategy to ensure the product is maintained in the desired state of control and meets both Quality and Business objectives. The Molecule Steward (Sr Director) is responsible for developing and delivering the technical elements of the GSC strategy for long‑acting injectable products with the GSC Strategic Lead. The Sr Director‑Molecule Steward Lead will be the recognized expert in long‑acting injectable products and in addition to strategic technical leadership, the role will be expected to provide deep technical expertise where required to ensure highest levels of quality and robustness.
Key Responsibilities
- Manage a group of Molecule Stewards (5‑10) accountable for end‑to‑end technical leadership of various pipeline and in‑line programs.
- Recruit and develop a world‑class team.
- Serve on Molecule Steward leadership team to drive and improve portfolio and organizational excellence.
- Define and own the technical strategy through a product's lifecycle including product transfers from R&D to GSK sites / External manufacturing sites & Site to Site, Product Performance Qualification and Ongoing Continuous Process Verification, leading Product Technical Lifecycle Team (PTLT) and yearly Manufacturing Robustness Review Board meetings (MRRB).
- Accountable for developing and delivering the Technical Lifecycle Plan (TLCP) including major geographical expansion, new technologies and second generation programs impacting the manufacturing process, analytical process, pack, device, and associated specifications.
- Ensure that product history and knowledge from development through the product's lifecycle is maintained and aligns with knowledge management standards for the product or dose form within the Global Supply Chain network.
- Provide technical leadership and subject matter expertise for multi‑site investigations and/or critical deviations, troubleshooting, and major change programmes across supply nodes.
- Stay current and maintain solid knowledge and understanding of complex scientific subject matter as well as evolving regulatory policies and guidelines and industry best practices.
- Co‑ordinate the technical review of regulatory submissions and responses to technical questions across MSAT.
- Represent MSAT and provide an MSAT single point accountable decision maker for GSC strategic team, CMC team, for established and new products.
- Develop and manage strong collaborations with technical staff across the Supply Chain sites, MSAT & R&D and maintain and develop technical talent through mentoring.
- Manage stakeholders effectively.
- Demonstrate knowledge of risk management approaches.
Basic Qualifications
- Bachelor's degree in life sciences, pharmaceutical sciences, biochemical engineering, or a related field.
- Experience in biopharmaceutical development, or a related scientific area.
- Experience supporting molecule program management across preclinical and/or clinical stages.
- Experience working within cross‑functional, matrixed development teams.
- Experience working within external regulatory frameworks (e.g., FDA, EMA, MHRA, PMDA) in a pharmaceutical or biologics development environment.
- Experience supporting technology transfer activities within a product development environment.
Preferred Qualifications
- PHD or Masters degree is preferred.
- Strong communication skills in English and experience presenting technical information to diverse audiences.
- Experience using risk‑based approaches and project management tools.
- Knowledge of global regulatory pathways for clinical development.
- Comfort working in matrixed and cross‑cultural teams.
Work Location
This role is based in Upper Providence PA, Waltham MA or Durham NC and United Kingdom (GSK HQ, London or Ware) / Wavre, Belgium / Aranda, Spain / Evreux, France. It offers a hybrid working model, combining on‑site and remote work.
Salary ranges for U.S. locations: $220,275 to $367,125. Salary and benefits details are provided in the benefits section below.
Benefits
Annual bonus and eligibility to participate in our share‑based long‑term incentive program. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. The U.S. benefits summary can be explored on the GSK US Benefits Summary website.
Equal Opportunity Employer
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Senior Director-Molecule Steward Lead employer: ENGINEERINGUK
Contact Detail:
ENGINEERINGUK Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Director-Molecule Steward Lead
✨Tip Number 1
Network like a pro! Reach out to current employees at the company through LinkedIn or industry events. A friendly chat can give you insider info and might just get your foot in the door.
✨Tip Number 2
Prepare for interviews by researching the latest trends in biopharmaceuticals and smart manufacturing technologies. Show us you’re not just a candidate, but a passionate expert ready to lead!
✨Tip Number 3
Practice your pitch! Be ready to explain how your experience aligns with the role of Senior Director-Molecule Steward Lead. We want to hear how you can drive innovation and quality in our supply chain.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team.
We think you need these skills to ace Senior Director-Molecule Steward Lead
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Senior Director-Molecule Steward Lead role. Highlight your relevant experience in biopharmaceutical development and any leadership roles you've held. We want to see how your skills align with our mission!
Showcase Your Technical Expertise: Don’t shy away from detailing your technical knowledge, especially around long-acting injectable products and regulatory frameworks. We’re looking for someone who can bring deep expertise to the table, so let us know what you’ve got!
Be Clear and Concise: When writing your application, keep it clear and to the point. Use straightforward language and avoid jargon unless necessary. We appreciate a well-structured application that makes it easy for us to see your qualifications.
Apply Through Our Website: We encourage you to submit your application through our website. It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at ENGINEERINGUK
✨Know Your Molecules
Make sure you have a solid understanding of long-acting injectable products and their lifecycle. Brush up on the latest advancements in biopharmaceutical development and be ready to discuss how these innovations can impact quality and productivity.
✨Showcase Your Leadership Skills
As a Senior Director, you'll need to demonstrate your ability to lead and develop a world-class team. Prepare examples of how you've successfully managed teams in the past, focusing on recruitment, mentoring, and driving organisational excellence.
✨Understand Regulatory Frameworks
Familiarise yourself with global regulatory pathways and guidelines, especially those relevant to FDA, EMA, and other authorities. Be prepared to discuss how you've navigated these frameworks in previous roles and how you can apply that knowledge here.
✨Communicate Effectively
Strong communication skills are key for this role. Practice presenting complex technical information clearly and concisely, as you'll need to engage with diverse audiences. Think about how you can tailor your message to different stakeholders during the interview.