Senior QA Officer - Consult : Job Details

Senior QA Officer

Consult

Job Location : Nottingham, UK

Posted on : 11/12/2024 - Valid Till : 22/01/2025

Job Description :

Senior QA Officer Nottingham

Our client, a leading pharmaceutical CDMO specialising in the development and manufacture of innovative pharmaceutical products, is undergoing significant expansion due to growing international demand. With a state-of-the-art GMP manufacturing facility and a comprehensive drug development portfolio, now is the perfect time to join this dynamic and forward-thinking team.

This is an opportunity to be part of a growing company at the forefront of pharmaceutical development. If you’re looking for a challenging and rewarding role with real impact, this could be the perfect fit for you.

My client is seeking a skilled and experienced Senior QA Officer to play a pivotal role within the established QA team. This customer-facing position offers the opportunity to work on a range of exciting projects, collaborating closely with cross-functional teams to deliver high-quality pharmaceutical solutions.

Key Responsibilities:

As the Senior QA Officer, you will:

  • Act as the QA representative on both new and existing project teams, ensuring quality actions are effectively managed.
  • Provide expert advice on GMP-related matters and support formulation, manufacturing, and analytical investigations.
  • Review manufacturing and analytical data, deviations, CAPAs, and change controls to ensure the release of investigational medicinal products meets quality standards.
  • Lead quality-related investigations, including deviations and CAPAs, while proactively engaging in continuous improvement activities.
  • Be a key point of contact for client and regulatory audits, representing the QA team and maintaining the Quality System.
  • Author quality-related documents and ensure compliance with all regulatory requirements.

About You:

To be successful in this role, you will have:

  • Demonstrable experience as a QA professional in a GMP-regulated environment with A deep understanding of cGMP regulations and quality management systems.
  • A proactive approach to identifying and resolving quality issues and a passion for driving continuous improvement.
  • Strong communication skills and proven experience working within cross-functional teams.
  • The ability to build strong relationships with both internal teams and external customers.

IndScientific123

If you're interested in the above role then please click apply or get in touch to discuss further.

Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful.

Salary : -

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