Job Description
QA Validation Consultant - Technical Writer
Location: Munster
Contract Type: 12-Month Contract (Limited or Umbrella Company)
Start Date: Immediate
4/5 days onsite
Join the largest bulk biopharmaceutical manufacturer in Ireland as a Technical Writer We are seeking a skilled writer with a strong background in the biopharmaceutical industry to create and maintain essential documentation for manufacturing processes and quality systems. This is a 12-month contract with a chance to make a significant impact within a leading global company.
Experienced in QA Validation activities.
Execution of cleaning validation protocols.
Experience on writing and approving Deviations/ GMP.
Technical writing experience in writing site reports.
Key Responsibilities:
- Experienced Technical writer.
- Experience in Deviation and investigation writing and data review.
- Experience in Validation specifically CIP/SIP validation or QA background.
- Experience in assessment of CIP/ SIP issues during study runs and close.
- Experience in cleaning validation/ SIP results reporting review beneficial.
- Capable of managing a large program, so project management skills would be desirable.
- An understanding of manufacturing and CIP/ SIP Validation equipment.
- Generate/review/Approval of CIP/ SIP protocols.
- Generation of Summary Reports and strong quality background essential.
- Experience in continuing validation and generation of assessments.
- Schedule of Cleaning/ SIP activities with Manufacturing.
- Follow all EHS/Safety SOP/Policies.
- Actively look for Continuous improvements.
To apply, please submit your CV and cover letter
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.