At a Glance
- Tasks: Lead the Quality department, ensuring compliance and managing quality systems.
- Company: Movianto is a top pharmaceutical supply chain partner focused on quality logistics.
- Benefits: Enjoy 33 days annual leave, discounted gym membership, and flexible pay options.
- Other info: This role involves national travel and occasional trips to Europe.
- Why this job: Make a real impact in healthcare while developing your leadership skills in a supportive environment.
- Qualifications: Experience in Quality roles within pharmaceuticals, strong leadership, and knowledge of GDP regulations required.
The predicted salary is between 36000 - 60000 £ per year.
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.
#J-18808-LjbffrQuality Manager & Responsible Person in Lutterworth employer: Movianto
Movianto is an exceptional employer, offering a supportive work culture that prioritises employee well-being and professional growth. With benefits such as 33 days of annual leave, flexible pay options, and access to health services, employees are empowered to thrive both personally and professionally. Located in Lutterworth, this role provides the opportunity to lead a dedicated team in ensuring the highest quality standards in pharmaceutical distribution, making a meaningful impact in the healthcare sector.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Manager & Responsible Person in Lutterworth
✨Tip Number 1
Familiarise yourself with the latest MHRA regulations and GDP guidelines. Being well-versed in these areas will not only boost your confidence during interviews but also demonstrate your commitment to compliance and quality management.
✨Tip Number 2
Network with professionals in the pharmaceutical quality sector. Attend industry events or join relevant online forums to connect with others who can provide insights or even referrals for the Quality Manager position at Movianto.
✨Tip Number 3
Prepare to discuss your leadership experience in detail. Think of specific examples where you've successfully managed a quality team or implemented quality systems, as this will be crucial in showcasing your fit for the role.
✨Tip Number 4
Research Movianto's operations and recent developments in the pharmaceutical distribution field. Understanding their business model and challenges will help you tailor your conversation during interviews and show that you're genuinely interested in contributing to their success.
We think you need these skills to ace Quality Manager & Responsible Person in Lutterworth
Some tips for your application 🫡
Understand the Role:Before applying, make sure you fully understand the responsibilities of a Quality Manager and Responsible Person. Familiarise yourself with the key requirements such as compliance with MHRA regulations and ISO standards.
Tailor Your CV:Highlight your relevant experience in Quality and Regulatory roles within pharmaceuticals or medical devices. Emphasise your leadership skills and any specific qualifications like Lead Auditor that align with the job description.
Craft a Compelling Cover Letter:Write a cover letter that showcases your passion for quality management and your understanding of Good Distribution Practice (GDP). Mention how your background makes you a suitable candidate for the role at Movianto.
Proofread Your Application:Before submitting, carefully proofread your CV and cover letter for any errors. Ensure that all information is clear, concise, and relevant to the position to make a strong impression.
How to prepare for a job interview at Movianto
✨Showcase Your Regulatory Knowledge
Make sure to highlight your understanding of GDP legislation and MHRA regulations during the interview. Be prepared to discuss how you've applied this knowledge in previous roles, as it’s crucial for the Quality Manager position.
✨Demonstrate Leadership Skills
As a potential leader of the on-site Quality team, it's important to convey your leadership experience. Share examples of how you've coached or mentored team members in the past, and how you plan to foster a positive team environment at Movianto.
✨Prepare for Technical Questions
Expect technical questions related to quality systems, such as deviation handling and CAPA processes. Brush up on these topics and be ready to explain your approach to managing quality systems effectively.
✨Express Adaptability and Travel Readiness
Since the role involves national travel and occasional trips to Europe, express your willingness and readiness to travel. Share any relevant experiences that demonstrate your adaptability in different environments or situations.
