At a Glance
- Tasks: Lead quality oversight in GMP processes and ensure compliance for high-quality medicines.
- Company: Join a leading pharmaceutical company dedicated to patient care and innovative solutions.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: Shift-based role with a focus on continuous improvement and quality culture.
- 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 45000 - 55000 £ 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. We are an Equal Opportunity Employer.
Team Lead, Therapeutic Area Quality in London employer: Job Search Place Limited
At GSK, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises quality and innovation in the pharmaceutical industry. Our commitment to employee growth is evident through continuous training opportunities and a supportive environment that fosters collaboration and inclusivity. Located in Irvine, our state-of-the-art facilities enable you to be at the forefront of smart manufacturing technologies, ensuring that your contributions directly impact patient safety and product quality.
StudySmarter Expert Advice🤫
We think this is how you could land Team Lead, Therapeutic Area Quality in London
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We think you need these skills to ace Team Lead, Therapeutic Area Quality in London
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Job Search Place Limited!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Job Search Place Limited that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Job Search Place Limited!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Job Search Place Limited, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Job Search Place Limited
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Job Search Place Limited that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Job Search Place Limited’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
