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 as
the option to buy more. Get it your way with Wagesteam,as well as access to a rewards platform, 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!
For more information or if you have any questions, please email recruitment.uk@movianto.com.
Movianto / Walden Group is an equal opportunity employer. All tasks must be carried out in compliance with the company and country
legislation and practices, health and safety at work and environment guidelines relevant to the market in which the role is
operational in. Please note the list above is not exhaustive and we expect the post holder to be flexible within the framework of
the job definition. Movianto / Walden Group seeks to recruit and appoint the best available person for a job regardless of marital
/ civil partnership status, sex (including pregnancy), age, religion, belief, race, nationality and ethnic or national origin,
colour, sexual orientation or disability. Movianto / Walden Group apply all relevant Data Protection laws when processing your
Personal Data. If you choose to apply to this opportunity and share your CV or other personal information with Movianto/ Walden
Group, these details will be held by us in accordance with our privacy policy used by our team to contact you regarding this or
other relevant opportunities at Movianto/ Walden Group.