Product Quality Release Administrator
Role as a supporting member, in a busy and expanding area of the Biological Production team, responsible for the release of intermediate and final products in accordance with the Quality System.
Role Essential Duties & Responsibilities.
Conduct quality reviews of documentation associated with the manufacture intermediate materials & finished goods.
Ensure manufactured materials meet required testing specifications.
Ensure document compliance in accordance with Good Manufacturing Practices.
Check, complete material and resource transactions within our ERP system.
Create and/or Approve Certificates of Analysis/Conformity for final products.
Support production Team Leaders in the continual flow of work into and out of the production area, through liaising with Kitting, Shipping & Technical Support teams.
Perform other related duties as assigned.
An interest in Life Science Industry
Knowledge of QC, Manufacturing, Document control and Inventory management processes
Advanced knowledge of Microsoft Word and Excel.
Excellent organisational skills & an ability to work to short timelines.
Strong verbal and written communication skills are required.
Knowledge of QMS, QSR & ISO standards and requirements is desirable
Experience working with Electronic Quality Management Systems.
Experience working with ERP systems like Oracle.
Please forward CVs in the first instance to Leigh Sproston