Cleaning Validation Specialist - Biopharmaceutical - An ideal opportunity for a scientific specialist with cleaning validation
QA Validation Specialist - Bio Pharmaceutical
I am delighted to be working with a leading Cork Biopharma company on their ambition to attract a cleaning validation specialist for the QA Validation team.
Roles and Responsibilities: Develop validation plans for specific system implementation projects.
Execute (protocol generation, execution, and final package preparation and reports) cleaning validation activities related to the implementation of process, equipment & overall manufacturing
Represent Validation in multi-departmental meetings & project teams
Coordinate re validation activities involving cross-functional, multi-departmental teams including: Manufacturing, Process Sciences, Process Development, Quality Control, Quality Assurance Regulatory Affairs, and others
Participate in the change control program for modifications to qualified systems
Establish Site Validation Policies, through development, generation and implementation of validation master plans, guideline documents and SOP's.
The ideal candidate:
Will have a science background in QA, QC or Laboratory (GMP essential)
A level 8 Degree
Experience within QA/ cleaning validation in Pharma or Biopharma.
Hands on experience with Autoclaves, Swabbing, Sampling, CIP & thermal mapping
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.