Scientific
Scientific

Quality Officer

Liverpool

Scope

This is an excellent opportunity for an experienced pharmaceutical Quality Assurance professional to join a leading, global biopharmaceutical organisation based in the North West. This offers a fantastic chance to work for an innovative company that are at the forefront of medicine development and manufacturing across several key therapeutic areas.

Responsibilities

  • Implementation of Quality Management Systems (QMS)
  • Oversee product batch review and release both on and off-site
  • Supporting change control procedures and deviations
  • Supporting internal and external cGMP audits
  • Additional validation activities- reviewing validation reports for equipment and method development
  • Ensure overall compliance with cGMP MHRA regulations

About You

To be suitable for this role, you will have at least 2 years’ experience with pharmaceutical Quality Assurance as well as:

  • Experience with pharmaceutical Quality Systems
  • Ability to follow written procedures and evaluate systems and records
  • Good knowledge of IT systems
If you are interested in the above role then please apply or get in touch to discuss further.
Ed Curl Managed by Ed Curl
highlights
North West
Permanent
Technical
apply Posted - 17.09.2020

Apply Now

Phone *

Allowed files: Word, pdf and txt

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.