Quality Projects and Implementation Manager - 12 Month FTC
Movianto Bedford
Job Advert
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.
Benefits
We have an onsite gym in Bedford, offer discounted PureGym membership, 33days of annual leave including bank holidays as well asthe 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 thepharmaceutical 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,
- 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
- 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
- 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
- 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.
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!
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