At a Glance
- Tasks: Ensure product quality and compliance in manufacturing processes at GSK's Ware site.
- Company: Join GSK, a leading pharmaceutical company dedicated to improving health.
- Benefits: Competitive salary, shift allowance, annual bonus, and professional development opportunities.
- Other info: Work in a supportive team with excellent career growth potential.
- Why this job: Make a real impact on life-saving medicines while working in a dynamic environment.
- Qualifications: BSc in a relevant field and knowledge of Good Manufacturing Practices required.
The predicted salary is between 45000 - 55000 £ per year.
The Quality function promotes quality and compliance through the product life-cycle within the wider manufacturing and production operations at the GSK Ware Manufacturing Site. This entails monitoring all quality related systems, improvement procedures and documentation (including data and information), ensuring that products released have been manufactured, packaged and distributed according to all Regulatory and cGMP requirements (including appropriate certification for EU markets).
Reporting to a Quality Operations Manager, the Quality Manager on Shift (Operational QA) ensures that activities related to both manufacturing and non-manufacturing areas are carried out compliantly with SOPs and GMP and the impact on product quality and supporting quality systems is fully assessed and recorded. Ensure that products that are released and distributed to market conform to registered and regulatory requirements and are manufactured to cGMP.
Key Responsibilities
- To liaise with other functions as appropriate in dealing with incidents affecting product quality or compliance, ensuring that deviations from GMP, specifications or company standards are fully recorded, remediated and investigated.
- To include the review/endorsement of CAPA proposals and to provide Quality approval of GMP procedures and documents.
- Participate in management monitoring of Quality processes and support wider value stream management monitoring activities.
- Provide necessary support in the investigation of customer or vendor complaints.
- Identify potential quality issues within manufacturing/packing/warehouse operations or other non-manufacturing areas as appropriate (via inspection, GEMBA and process confirmation).
- Ensure manufacturing, packaging, Warehouse and wider support process changes are controlled appropriately and the impacts adequately assessed and monitored.
- Ensuring that product released/shipped conforms to the required quality standards.
- Provide quality oversight of facilities, equipment and personnel.
- Support Distribution Risk Assessments (if applicable).
- Coach staff in setting and maintaining appropriate quality and compliance standards and liaise with supported functions in providing quality guidance through TAP process, Gembas and quality meetings.
As part of the quality assurance team, you will promote team working and effective communication across the Ware site and across GSK's wider Quality functions (at other sites).
Please note that this role requires the successful applicant to be based/work in the GMP area for the site.
Shift
Please note that this role is aligned to the following shift: 24/5 (during the week) and 16/2 (on the weekend). The Monday to Friday shifts (during the week) operate on 12-hour shifts: Days (circa 6:40 to 19:00) and Nights (circa 18:40 to 7:00) working on a 2 or 3 (day or night) shift rotation. Please note that you will also need to work 2 weekends per month: 1 weekend on Earlies (circa 6:15 to 14:30) and 1 weekend on Lates (circa 14:00 to 22:15). Total working week will be circa 37.5hrs (on average across the month).
About You
As this role is multi-faceted and includes liaising with a wide variety of on-site production and operations teams, you will be a self-motivated person who has strong experience of working in quality and/or manufacturing at a complex manufacturing site. You will be resilient and calm under pressure, with strong people skills and a proven ability to influence people to achieve objectives and drive performance. You will have a strong continuous improvement mindset. Effective written and verbal communication and excellent interpersonal skills, as well as the ability to organise and prioritise workload are considered essential skills.
About Ware Manufacturing Site
Medicines at Ware are presented as either Respiratory devices or in Oral Solid Dose form. The site holds a unique position in our network as the only site responsible for launching the company's pipeline of new medicines in these dose forms, many of which are life saving medicines. A series of investments in new state‑of‑the‑art equipment are being made that will support the delivery of a record number of new products.
Closing Date for Applications
Monday 15th of June 2026 (COB).
Basic Qualifications
- BSc in Scientific, Technical or Engineering discipline (or equivalent experience, ideally gained working in a Pharmaceutical Manufacturing Facility or similar highly regulated industry).
- Knowledge of current Good Manufacturing Practice requirements.
- Knowledge and application of Quality Management Systems (QMS).
Benefits
- Competitive base Salary
- Shift allowance
- Annual bonus based on company performance
- Opportunities to partake in on-the-job training courses
- Opportunities for support for professional development and chartership (accreditations and professional bodies)
- Access to healthcare and wellbeing programmes
- Employee recognition programmes
Equal Opportunity
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.
Quality Manager (on Shift) in Ware employer: WISE Campaign
GSK is an exceptional employer, offering a dynamic work environment at the Ware Manufacturing Site, where you will play a crucial role in ensuring the quality and compliance of life-saving medicines. With competitive salaries, shift allowances, and robust professional development opportunities, GSK fosters a culture of continuous improvement and teamwork, empowering employees to thrive in their careers while contributing to meaningful healthcare advancements.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Manager (on Shift) in Ware
✨Tip Number 1
Network like a pro! Reach out to current employees at GSK or in the quality management field. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of GMP and QMS. Be ready to discuss how you've tackled quality issues in the past. Show them you're not just a fit for the role, but a passionate advocate for quality!
✨Tip Number 3
Practice your communication skills! Since this role involves liaising with various teams, being able to clearly express your thoughts and ideas is key. Try mock interviews with friends or use online resources to sharpen those skills.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining the GSK team and ready to contribute to their mission.
We think you need these skills to ace Quality Manager (on Shift) in Ware
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Quality Manager role. Highlight your experience in quality assurance and compliance, especially in a manufacturing environment. We want to see how your skills align with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality management and how your background makes you a perfect fit for our team. Keep it engaging and relevant to the job description.
Showcase Your Communication Skills:Effective communication is key in this role. In your application, demonstrate your written communication skills by being clear and concise. We love candidates who can express their thoughts well, so don’t hold back!
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. Plus, you’ll find all the details you need about the role and our company there!
How to prepare for a job interview at WISE Campaign
✨Know Your GMP and QMS
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and Quality Management Systems (QMS). Be ready to discuss how you've applied these in previous roles, as this will show your understanding of the regulatory environment and your ability to ensure compliance.
✨Prepare for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills. Think of examples where you've dealt with quality issues or compliance deviations. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly and effectively.
✨Showcase Your People Skills
As a Quality Manager, you'll need to liaise with various teams. Prepare to demonstrate your interpersonal skills by sharing experiences where you've influenced others or resolved conflicts. Highlight your ability to coach staff and promote teamwork.
✨Understand the Shift Requirements
Since this role involves specific shift patterns, be prepared to discuss your availability and adaptability. Show enthusiasm for working in a dynamic environment and explain how you manage work-life balance while meeting the demands of shift work.
