Job Description
A leading Biotech company based in Dublin is seeking an experienced Technical Writer to join their team on an initial 12 month hourly rate contract.
Main Responsibilities:
1. Generate, review & update Standard Operating Procedures.
2. Collaborate with Manufacturing/Inspection/Engineering regarding documentation changes/updates etc.
3. Generate protocols for execution in Manufacturing & Inspection in support of change controls, deviations & troubleshooting investigations with support from relevant SMEs.
4. Management of change controls for Manufacturing/Inspection/Engineering
5. Liaise with Quality Assurance to ensure that GMP standards are upheld at all times
6. Use specified software packages and standard procedures, responsible for compiling and maintaining all relevant documentation including SOPs.
7. Provide technical and clerical support to the manufacturing, inspection & engineering teams in the preparation of documentation, collation of data and tracking of SOPs
8. Ownership of minor deviations as required
Basic Qualifications:
9. Degree in Science or Engineering discipline
10. Significant experience in Chemistry/Microbiology/Engineering/Validation gained within a Biotech or Pharma
11. Experience working in a GMP environment
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.
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