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- Tasks: Lead a team of Molecule Stewards in innovative drug development and lifecycle management.
- Company: Join a leading biopharmaceutical company committed to innovation and excellence.
- Benefits: Competitive salary, comprehensive benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on mentorship and career progression.
- Why this job: Make a significant impact on groundbreaking drug products and drive industry advancements.
- Qualifications: Bachelor's degree in life sciences; experience in biopharmaceutical development preferred.
The predicted salary is between 100000 - 150000 £ per year.
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. The role provides strategic technical leadership to ensure successful new product introduction, launch, and continuous improvement across the lifecycle.
Position Summary: The Senior Director will drive program alignment across a portfolio of assets from Commit to Commercial Design through product sunset.
Key Responsibilities:
- Manage a group of Molecule Stewards (5‑10) accountable for end‑to‑end technical leadership of pipeline and in‑line programs, recruiting and developing a world‑class team.
- Serve on the Molecule Steward leadership team to drive portfolio excellence.
- Define and own the technical strategy through the product lifecycle, including technology transfers, process qualification, and risk management.
- Develop and deliver the Technical Lifecycle Plan (TLCP), supporting geographical expansion and new technologies.
- Maintain product history and knowledge alignment with global standards, serving as key input for process history files.
- Provide technical leadership on multi‑site investigations, deviations, troubleshooting, and major change programmes.
- Stay current on scientific developments, regulatory policies, and industry best practices.
- Coordinate technical review of regulatory submissions and responses across MSAT and other stakeholders.
- Act as MSAT single‑point accountable decision maker for GSC strategic and CMC teams, ensuring robust product control strategy.
- Collaborate with technical staff across supply chain sites, MSAT, and R&D, mentoring and developing technical talent.
- Manage stakeholders effectively and apply risk‑based 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).
- Experience supporting technology transfer activities within a product development environment.
Preferred Qualifications:
- PhD or Master’s degree.
- 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.
Senior Director-Molecule Steward Lead in Ware employer: WISE Campaign
Contact Detail:
WISE Campaign Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Director-Molecule Steward Lead in Ware
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at GSK or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their pipeline and recent developments in long-acting injectables. This will help you speak confidently about how your experience aligns with their needs.
✨Tip Number 3
Showcase your leadership skills! Be ready to discuss how you've managed teams and driven technical strategies in past roles. Use specific examples that highlight your ability to lead cross-functional teams effectively.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in joining our team at StudySmarter.
We think you need these skills to ace Senior Director-Molecule Steward Lead in Ware
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Senior Director role. Highlight your leadership in technical projects and any experience with molecule stewardship to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you're passionate about this role and how your background makes you the perfect fit for leading our Molecule Stewards.
Showcase Your Achievements: Don’t just list your responsibilities; share your achievements! Quantify your successes where possible, like improvements in product launches or team development, to demonstrate your impact.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!
How to prepare for a job interview at WISE Campaign
✨Know Your Molecule Inside Out
Make sure you have a deep understanding of the specific molecule or product you'll be discussing. Familiarise yourself with its lifecycle, from development to commercialisation, and be ready to talk about any challenges and successes you've encountered in similar roles.
✨Showcase Your Leadership Skills
As a Senior Director, you'll need to demonstrate your ability to lead and develop a team. Prepare examples of how you've successfully managed teams in the past, focusing on recruitment, mentoring, and driving portfolio excellence. Highlight your experience in cross-functional collaboration too!
✨Be Ready for Technical Questions
Expect to face technical questions related to drug substance, drug product, and regulatory frameworks. Brush up on your knowledge of technology transfers, process qualifications, and risk management strategies. Being able to discuss these topics confidently will set you apart.
✨Understand the Company’s Vision
Research GSK's current projects and their strategic goals. Be prepared to discuss how your experience aligns with their objectives, especially regarding innovative programmes and continuous improvement. Showing that you’re aligned with their vision can make a big difference!