At a Glance
- Tasks: Lead quality oversight in pharmaceutical manufacturing and ensure compliance with GMP standards.
- Company: Join GSK, a global biopharma leader dedicated to improving patient health.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: On-site role with shift-based pattern; supportive and inclusive workplace.
- Why this job: Make a real impact on patient safety and product quality in a dynamic environment.
- Qualifications: Degree in life sciences or equivalent experience in the pharmaceutical industry.
The predicted salary is between 46000 - 52000 £ per year.
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. Technology is transforming manufacturing, enabling us to increase speed, quality and scale of product supply. We seek the best minds to harness smart manufacturing technologies, including robotics, digital solutions and artificial intelligence, to deliver for patients.
Position Summary: To ensure adherence to GMP standards and procedures through independent oversight of GMP processes; to improve quality culture and continuous improvement; to maintain shift-based presence and be accountable for key quality decisions or escalations; to provide first-line support to operational areas and maintain inspection-readiness through independent checks.
Responsibilities:
- Ensure that all GMP processes and operational personnel adhere to current local or area-specific procedures, minimising risk of non-compliance and maintaining inspection readiness.
- Maintain presence across the area of responsibility and be first line of contact to support initial management of quality issues; be accountable for key quality decisions across activities such as initial impact assessments for deviations; provide guidance during GMP activities to detect potential quality issues and enable timely interventions.
- Provide Quality support for site management monitoring audits across GMP areas.
- Ensure adherence to the frequency of oversight mandated in the Quality oversight schedule.
- Check facilities are maintained in a good state per local housekeeping standards and escalate deviations with timely actions.
- Role model GPS standards by participating in tiered accountability meetings (e.g., production changeover meetings).
- Foster a Quality Starts With Me (QSWM) culture by coaching employees on procedures, doing the right thing, and explaining the impact of non-compliance on product quality and patient safety.
- Provide out-of-hours support for SLE process confirmation of non-routine or high-risk activities.
Qualifications:
- Degree, HND/HNC or equivalent in life science, chemistry, microbiology or related subject, or substantial practical laboratory experience.
- Experience of the pharmaceutical industry with strong knowledge of QMS/GMP and related manufacturing aspects; experience in resolving cGMP issues.
- Strong influencing, communication and coaching skills; ability to contribute to department project activities.
Preferred Qualifications:
- Familiarity with investigation tools and CAPA processes.
- Experience preparing for audits and inspections.
- Prior on-site pharmaceutical manufacturing experience.
Working Pattern: On-site at Irvine with shift-based pattern; exact shift details to be discussed during recruitment.
Inclusion: We welcome applicants from all backgrounds and are committed to a supportive and inclusive environment. If you need a reasonable adjustment to the application or interview process, please tell us and we will support you.
Ready to apply? If this role fits your skills and ambitions, apply by describing how you would lead the team, deliver quality results and make a meaningful impact.
Why GSK? GSK is a global biopharma company focused on uniting science, technology and talent to get ahead of disease together. We are an Equal Opportunity Employer. We encourage agile working where possible and welcome adjustments to the process if needed.
Team Lead, Therapeutic Area Quality employer: WISE Campaign
GSK is an exceptional employer that prioritises quality and innovation in the biopharmaceutical sector, offering a dynamic work environment in Irvine. With a strong commitment to employee growth, GSK fosters a culture of continuous improvement and inclusivity, providing opportunities for professional development and the chance to make a meaningful impact on patient care. Employees benefit from a supportive atmosphere that encourages agile working and values diverse perspectives, making it an ideal place for those looking to advance their careers in a forward-thinking company.
StudySmarter Expert Advice🤫
We think this is how you could land Team Lead, Therapeutic Area Quality
✨Tip Number 1
Network like a pro! Reach out to current employees in the pharmaceutical industry, especially those at GSK. A friendly chat can give us insider info and maybe even a referral.
✨Tip Number 2
Prepare for the interview by brushing up on GMP standards and quality oversight processes. We want to show that we know our stuff and can handle any quality issues that come our way.
✨Tip Number 3
Practice our answers to common interview questions, especially around leadership and quality culture. We need to demonstrate how we would lead the team and ensure compliance.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to get noticed and ensures our application is seen by the right people. Let’s make it happen!
We think you need these skills to ace Team Lead, Therapeutic Area Quality
Some tips for your application 🫡
Show Your Passion for Quality:When writing your application, let your enthusiasm for quality and compliance shine through. We want to see how you can contribute to our mission of delivering high-quality medicines and vaccines.
Be Specific About Your Experience:Don’t just list your qualifications; give us examples of how you've tackled GMP issues or led quality initiatives in the past. This helps us understand your hands-on experience and how it aligns with our needs.
Tailor Your Application:Make sure to customise your application to reflect the specific requirements of the Team Lead role. Highlight your relevant skills and experiences that match the job description, so we can see why you're a great fit.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at WISE Campaign
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practices (GMP) and Quality Management Systems (QMS). Be ready to discuss how you've applied these in your previous roles, especially in resolving cGMP issues. This shows you're not just familiar with the terms but can actually implement them.
✨Showcase Your Coaching Skills
Since the role involves fostering a quality culture, think of examples where you've successfully coached or influenced others. Prepare to share specific instances where your guidance led to improved compliance or quality outcomes. This will highlight your leadership potential.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to quality issues or GMP non-compliance. Practice articulating your thought process on how you'd handle these scenarios, focusing on timely interventions and decision-making. This demonstrates your problem-solving skills.
✨Prepare for Audit Discussions
Given the emphasis on inspection readiness, be prepared to discuss your experience with audits and inspections. Highlight any tools or processes you've used to prepare for these events, and how you ensured compliance. This will show your proactive approach to quality oversight.
