Are you a QA officer with GMP experience within the Pharmaceutical industry?

This role provides QA oversight to operational activities across the manufacturing facility, this includes laboratory operations, warehouse and aseptically filled products.

Role:

  • Physical and Online review of GMP records from equipment logbooks and output such as FMS and sterilization cycles to batch manufacturing records and QC testing.·
  • Batch records with associates LIMS & SAP.·
  • Supervision of cleanrooms/support areas; comportment & compliance to SOP's.·
  • Supervision of packaging areas; comportment & compliance to SOP's.·
  • Proactive generation and timely investigation/review/implementation of change controls.·
  • Local area & local system audits.·
  • Training/coaching of staff & QA peers.·
  • Communicate effectively with other employees and participate with them in planning and problem-solving activities, as required.·
  • Media fill observation, incubation, reading & report writing.·
  • Review of validation documentation.

Requirement's: ·

  • Relevant science-based degree; e.g. Chemistry, Biology, Pharmacy.·
  • Substantial experience working within a pharmaceutical quality function, ideally direct QA experience with steriles manufacturing.·
  • Working knowledge of the principles and guidelines for GMP as set out in the 'Orange Guide.'·
  • Excellent interpersonal skills with the ability to appropriately challenge other's behaviours.·
  • Excellent report writing skills.·
  • Good time management.·
  • Must be willing to work shifts to cover 24/7 operations.

    For more information regarding this position or any others, please call Bal on 0121 728 8455 or email Balbir.Panesar@srgtalent.com