Description
Activities will include change control, nonconformance investigation, supplier qualification, incoming materials release, batch release, annual product review and validation compliance activities.Main duties and responsibilities:
To provide support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met.
To carry out tasks related to the administration of site nonconformance management systems including review and/or approval of investigation.
Carries out tasks relating to the management of site change control systems.
Supports system qualification and process validation activities.
Carries out tasks related to the administration of site supplier approval systems.
Carries out tasks related to the management of batch records design and approval.
ESSENTIAL:
* Bachelors Degree in a scientific/technical discipline required
* A minimum of 5 years' experience in a quality, manufacturing, validation or compliance role within the biological and/or pharmaceutical industry.
* Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.
This is an exciting opportunity to join a leading company with competitive hourly rates. If you would like to apply please contact Sarah Irvine on . We also offer vouchers for any successful referrals so if you know of anyone who may be looking please feel free to get in touch.