Senior Technical Writer

  • Dublin
  • Temporary 12 months
  • JO-1908-64725_1567437943

Summary

Great Opportunity to join a multinational pharmaceutical company in Dublin.

Responsibilities

  • Develop, review and update engineering, manufacturing, & inspection Standard Operating Procedures.
  • Liaise with Manufacturing/Inspection/Engineering regarding documentation changes in an effective and timely manner.
  • Develop protocols for execution in Manufacturing & Inspection in support of change controls, non-conformances & troubleshooting investigations with support from relevant SMEs.
  • Involvement in projects as part of continuous process improvement and / or troubleshooting,
  • Ownership of change controls for Manufacturing/Inspection/Engineering
  • Issuance and updates of paper batch records in line with the production schedule.
  • Liaise with Quality Assurance to ensure that GMP standards are maintained in line with the current OS
  • Support the production support team in reducing document turnaround times.
  • Use specified software packages and standard procedures, responsible for compiling and maintaining all relevant documentation including SOPs.
  • Provide technical and clerical support to the manufacturing, inspection & engineering teams in the preparation of documentation, collation of data and tracking of SOPs
  • Ownership of Level 1 non-conformances

Basic Qualifications:

  • Educated to degree level or equivalent.
  • Significant experience in Chemistry/Microbiology/Engineering/Validation gained within a biotech, pharma or health care organization.

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