Quality Manager & Responsible Person
| Posting date: | 14 July 2025 |
|---|---|
| Salary: | £40,000 to £50,000 per year |
| Hours: | Full time |
| Closing date: | 13 August 2025 |
| Location: | Lutterworth, Leicestershire, LE17 4XZ |
| Company: | Movianto |
| Job type: | Contract |
| Job reference: | REC002417_1752482695 |
Summary
Ready to take the lead in pharmaceutical distribution quality? Join Movianto as our Quality Manager and Responsible Person! We are hiring in Lutterworth.
Benefits
- No weekend or bank holiday working
- Discounted gym membership
- 33 days annual leave (including bank holidays)
- Holiday Purchase scheme
- Flexible pay through Wagestream
- Life Assurance
- Up to 4% Employer Pension Contribution
- Access to Simply Health
- 24/7 GP, physiotherapy and counselling through our EAP service
- Cycle to Work scheme
- Access to MyRewards, a benefits platform
Who we are
Movianto is a leading pharmaceutical supply chain solutions partner offering best-in-class logistics quality for the pharmaceutical, biotech, medical device and diagnostic industries.
Purpose of the role
This is a key leadership role, responsible for managing the operational performance of our Quality department and ensuring compliance with our Quality Management System, MHRA regulations, and ISO standards. You will also act as the named Responsible Person for our MHRA licences, ensuring adherence to Good Distribution Practice (GDP) guidelines and overseeing quality activities across the site.
How you will make an impact at as a Quality RP Movianto:
- Leading the on-site Quality team, providing coaching, training, and mentoring.
- Maintaining compliance with GxP, ISO 9001, ISO 13485, and other regulatory standards.
- Managing quality systems such as deviation handling, CAPA, and supplier management.
- Conducting root cause analysis, audits, and hosting regulatory inspections.
- Acting as Head of Quality Control for our secondary repackaging licence (Bedford-specific).
- Representing the Quality department in client meetings and ensuring high standards across operations.
What it will take to thrive at as a Quality Manager and Responsible Person at Movianto:
- Proven experience in Quality/Regulatory roles within pharmaceuticals or medical devices.
- Extensive knowledge of GDP legislation and MHRA regulations.
- Strong leadership skills and experience managing quality systems.
- Eligible to act as a named Responsible Person on WDA (H) and WDA (V) licences.
- Lead Auditor qualification (desirable) and advanced PC literacy
- This role involves national travel and occasional European trips, making it ideal for someone adaptable and ready to make an impact.
Ready to make a difference with us? Apply now and become a part of our dedicated team!
For more information or if you have any questions you can email - recruitment.uk @ movianto.com.
Delivering healthcare across the nation - Movianto UK
Movianto/Walden Group is an equal opportunity employer committed to diversity and inclusion. We comply with all relevant laws, health and safety regulations, and environmental guidelines. The role requires flexibility within the job definition, and the responsibilities listed are not exhaustive.
We recruit based on merit, regardless of marital or civil partnership status, sex (including pregnancy), age, religion, belief, race, nationality, ethnicity, sexual orientation, or disability. As a Disability Confident Leader and Armed Forces-friendly organisation, we are dedicated to fostering an inclusive workplace.
By applying, you agree to the processing of your personal data in line with our privacy policy, which ensures your details are handled appropriately for this or other relevant opportunities within Movianto/Walden Group.