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: Supportive workplace that values diversity and offers flexible working arrangements.
- 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 in London employer: WISE Campaign
GSK is an exceptional employer that prioritises quality and innovation in the biopharmaceutical industry. With a strong commitment to employee growth, we foster a culture of continuous improvement and inclusivity, ensuring that every team member has the opportunity to thrive in their career. Located in Irvine, our state-of-the-art facilities and focus on smart manufacturing technologies create a dynamic work environment where you can make a meaningful impact on patient care.
StudySmarter Expert Advice🤫
We think this is how you could land Team Lead, Therapeutic Area Quality in London
✨Tip Number 1
Get to know the company inside out! Research their values, recent projects, and any news related to their quality standards. This will help you tailor your conversations and show that you're genuinely interested in being part of their team.
✨Tip Number 2
Network like a pro! Connect with current employees on LinkedIn or attend industry events. Having someone vouch for you can make a huge difference when it comes to landing that interview.
✨Tip Number 3
Prepare for the interview by practising common questions related to GMP and quality oversight. Think about how your past experiences align with the role and be ready to share specific examples that highlight your skills.
✨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 the team!
We think you need these skills to ace Team Lead, Therapeutic Area Quality in London
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, so share specific examples of your experience in GMP and quality oversight.
Tailor Your Application:Make sure to customise your application to highlight the skills and experiences that align with the job description. We’re looking for someone who understands the pharmaceutical industry and has a strong grasp of QMS/GMP, so don’t hold back on showcasing your relevant background.
Be Clear and Concise:Keep your application straightforward and to the point. We appreciate clarity, so avoid jargon and ensure your key achievements and qualifications are easy to spot. This will help us quickly see why you’d be a great fit for the role.
Apply Through Our Website:Don’t forget 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 makes the whole process smoother for everyone involved.
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 will show that you understand the core of the role and can hit the ground running.
✨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 demonstrate your ability to lead and inspire a team.
✨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 and decision-making skills in these scenarios. This will help interviewers see how you handle pressure and make critical decisions.
✨Prepare Questions About the Company Culture
Research GSK's values and their commitment to a supportive environment. Prepare thoughtful questions about how they foster a 'Quality Starts With Me' culture. This shows your genuine interest in the company and helps you assess if it’s the right fit for you.
