At a Glance
- Tasks: Collaborate on technical strategies and support drug manufacturing processes.
- Company: Join GSK, a leader in pharmaceutical innovation and global supply.
- Benefits: Comprehensive benefits, career growth, and a commitment to diversity.
- Other info: Opportunity to work with global teams and enhance your technical skills.
- Why this job: Make a real impact in the pharmaceutical industry with cutting-edge technology.
- Qualifications: Bachelor's degree in a scientific field and 5+ years in technical operations.
The predicted salary is between 60000 - 80000 € per year.
The Global Manufacturing Science and Technology (MSAT) organization is a network focused function which provides strategic direction, technical and operations support to ensure that GSK Global Supply Chain network goals and objectives are achieved, through a focused strategy execution. As an accountable Subject Matter Expert (SME), this role will collaborate closely with internal and external stakeholders, to support the ongoing commercial manufacture of large molecule Drug substance and/or sterile Drug Product, ensuring technical lifecycle support and execute MSAT/EM technical strategy and activities for manufacturing processes including routine operation, field, technical support, and validation.
Responsibilities
- Execute technical strategy and represent MSAT Technical Operations for External Manufacturing in relevant PQTS teams.
- Ensure support for CMOs in establishing maintenance, performance of standards, and technical transfers of established products or transfers between CMOs.
- Support CMO for audit documentation, inspection readiness, and prepare local teams during audits.
- Ensure critical lifecycle activities: CPV Change control, Deviation investigation and resolution, CAPAs, Waste mapping, Performance of standards, Continuous Improvement (financial, process, etc).
Qualifications
- Bachelor's degree in Pharmaceutical Sciences, Engineering, Chemistry, Biology, or a related scientific field.
- 5+ years' experience in drug substance and/or drug product (including device) technical operations in pharmaceutical or biologics manufacturing.
- Experience of the pharmaceutical current best practice in analytical and manufacturing technologies, validation and GMP compliance.
- Experience with managing product life cycle activities.
- Lead technical investigations, perform root cause analysis, manage change control, and develop corrective and preventive actions (CAPA).
- Experience collaborating with external manufacturing partners.
Preferred
- Advanced degree (Master's or PhD) in a relevant scientific or engineering discipline.
- Demonstrated success identifying and leading continuous improvement.
- Certification or formal training in project management, risk management, or continuous improvement methods (e.g., Lean or Six Sigma).
- Experience supporting regulatory inspections and preparing technical responses.
- Proven track record of successful technology transfers to CMOs or external partners.
- Experience coaching and developing technical capability across multi-site or global teams.
Comprehensive benefits program available for US employees. 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.
SME - MSAT EM Technical Operations DS/DP employer: WISE Campaign
GSK is an exceptional employer that fosters a collaborative and innovative work culture, particularly in the vibrant field of pharmaceutical manufacturing. Employees benefit from comprehensive support for professional growth, including opportunities for continuous improvement and technical development, all while contributing to meaningful projects that impact global health. Located in a dynamic environment, GSK prioritises employee well-being and inclusivity, making it a rewarding place to advance your career.
StudySmarter Expert Advice🤫
We think this is how you could land SME - MSAT EM Technical Operations DS/DP
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in MSAT or related fields. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge and recent advancements in drug substance and product manufacturing. We want you to showcase your expertise and how it aligns with GSK's goals!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your enthusiasm for the role. It keeps you fresh in their minds!
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, you’ll find all the latest job openings tailored to your skills and interests.
We think you need these skills to ace SME - MSAT EM Technical Operations DS/DP
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the job description. Highlight your background in pharmaceutical sciences or engineering, and any relevant technical operations experience you've got. We want to see how you fit into our MSAT team!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about the role and how your experience aligns with our goals at StudySmarter. Don't forget to mention any specific projects or achievements that showcase your expertise in drug substance or product manufacturing.
Showcase Your Collaboration Skills:Since this role involves working closely with internal and external stakeholders, make sure to highlight your teamwork and communication skills. Share examples of how you've successfully collaborated on technical projects or supported audits in the past. We love a good team player!
Apply Through Our Website:We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, we can’t wait to see what you bring to the table!
How to prepare for a job interview at WISE Campaign
✨Know Your Stuff
Make sure you brush up on your knowledge of drug substance and drug product technical operations. Familiarise yourself with the latest trends in pharmaceutical manufacturing, GMP compliance, and analytical technologies. This will help you answer questions confidently and demonstrate your expertise.
✨Showcase Your Collaboration Skills
Since this role involves working closely with internal and external stakeholders, be prepared to discuss your experience in collaboration. Think of specific examples where you've successfully partnered with others, especially in a manufacturing context, and how that led to improved outcomes.
✨Prepare for Technical Questions
Expect to face technical questions related to lifecycle activities, change control, and CAPA processes. Review your past experiences and be ready to explain how you've handled deviations or led investigations. Use the STAR method (Situation, Task, Action, Result) to structure your answers.
✨Demonstrate Continuous Improvement Mindset
Highlight any experience you have with continuous improvement methodologies like Lean or Six Sigma. Be ready to discuss specific projects where you've identified inefficiencies and implemented solutions. This shows that you're proactive and committed to enhancing processes.
