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Quality Projects and Implementation Manager

2 months ago

Central Bedfordshire, United Kingdom Movianto UK Full time

Are you ready to lead a key transformation within the pharmaceutical industry? We are looking for a driven and knowledgeable Quality Projects and Implementation Manager to join our team on a 12 Month FTC.



Find out if this opportunity is a good fit by reading all of the information that follows below.

Benefits

We have an onsite gym in Bedford, offer discounted PureGym membership, 33days of annual leave including bank holidays as well as the option to buy more, as well as access to a rewards platform, free flu vaccine, a workplace pension, access to simply health and other perks. You’ll also have access to My Rewards our benefits platform offering a variety of high street discounts, cashback and savings.


Purpose of the role

This role will focus on optimising our quality processes and systems, ensuring we meet the ever-evolving demands of the pharmaceutical industry while maintaining full compliance. Reporting to the Quality Director, you'll work closely with cross-functional teams to drive operational efficiency and continuous improvement.


Key Responsibilities

  • Lead the continued rollout of the Electronic Quality Management System (EQMS), with a focus on modules such as Non-Conformance, CAPA, Change Control, and Continuous Improvement.
  • Oversee client integration processes, ensuring compliance with change control and risk assessments.
  • Host and support client audits, providing timely responses to audit reports and maintaining Quality Technical Agreements.
  • Collaborate with the Commercial Team to support new business inquiries, ensuring client requirements are fully integrated into our Quality Management System.
  • Build and maintain strong relationships with external client quality teams, delivering clear communication and exceeding client expectations.


Technical and Behavioural Skills

  • Proven ability to work independently and within a team, delivering high performance in a fast-paced, deadline-driven environment.
  • Excellent communication and presentation skills, with confidence in engaging with diverse audiences.
  • Strong problem-solving abilities, organisational skills, and proficiency in managing multiple priorities.
  • In-depth knowledge of Good Distribution Practices (GDP), Good Manufacturing Practices (GMP), and pharmaceutical compliance standards.
  • Experience in pharmaceutical product transportation, storage, and distribution.

Desirable Qualifications:

  • RP Gold Standard Training.
  • Qualified Lead Auditor certification.
  • Experience as a Registered Responsible Person (RP) in the pharmaceutical industry.

This is an exciting opportunity to play a key role in shaping the future of our business, as we continuously improve and maintain the highest standards of quality and compliance. If you have the expertise and drive to make a real impact, we’d love to hear from you