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Technical Writer

  • Job reference: 929142
  • Location: Dublin South, Dublin
  • Salary: Negotiable
  • Job type: Contract
  • Sector: Life Sciences, Quality, Compliance, Regulatory Affairs
  • Date posted: 15/01/2020

Orion Group Sciences are looking for a Technical Writer for our multinational pharmaceutical client based in the South of Dublin area on an initial 12-month contract with the potential to extend.


Job Purpose
The activities performed in the role of Engineering Technical Writer include: develop, review and update calibration operating procedures, involvement in engineering meetings as part of coordination of specification changes that will lead to updates to SOPs and BOM & involvement in projects as part of continuous process improvement Information Systems Tech Writer

As a member of the Information Systems team, the individual will act as an IS Tech Writer and will support complex and challenging initiatives across the full breadth of Information Systems.

Main Responsibilities of the role

  • Develop, review and update engineering, manufacturing, & inspection Standard Operating Procedures
  • Develop protocols for execution in Manufacturing & Inspection in support of change controls, nonconformances & troubleshooting investigations with support from relevant SMEs Liaise with Manufacturing/Inspection/Engineering regarding documentation changes in an effective and timely manner
  • 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 production schedule
  • Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current OS Support 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
  • Update design documents, and Business builds
  • Writing Protocols as required for projects / deliver to tight timelines

Desired Experience and Background of the successful candidate

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

Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

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