Pharma Technical Writer (GMP & Veeva) – Contract

LSC, Life Science Consultants; Cork; On-site; EUR 55,000 - 75,000; Full time

Job summary

LSC, Life Science Consultants, is seeking a Technical Writer for a Cork-based biopharmaceutical contract role. The role focuses on developing and maintaining site documentation, including BPDs, SOPs, and reports, ensuring data integrity and regulatory compliance.

The ideal candidate will have a science or engineering background and substantial technical writing experience within regulated pharma or biotech environments, with familiarity with GMP documentation and ALCOA principles, and hands-on

Qualifications

• Third level qualification in a Science or Engineering discipline and/or extensive relevant technical writing experience.

Responsibilities

• Develop and continuously improve the site documentation management strategy.
• Draft, review and approve BPDs, SOPs, technical protocols and reports, forms, work instructions and other controlled documentation.
• Produce accurate, high-quality documentation in line with data integrity, ALCOA and regulatory compliance requirements.
• Act as an SME for Veeva Quality Documents and ComplianceWire, providing guidance and support to colleagues.
• Collaborate with technical SMEs and cross-functional teams to ensure documentation accurately reflects technical and business requirements.
• Support the transition of documentation into Veeva Quality Documents and assist with training materials, guides and e-learning modules.

Skills

Technical writing

Document management

Regulated environment

Data integrity/ALCOA

Education

Science or Engineering degree

Tools

Veeva Quality Documents

ComplianceWire

Job description

LSC, Life Science Consultants, is seeking a Technical Writer for a Cork-based biopharmaceutical contract role. The role focuses on developing and maintaining site documentation, including BPDs, SOPs, and reports, ensuring data integrity and regulatory compliance.

The ideal candidate will have a science or engineering background and substantial technical writing experience within regulated pharma or biotech environments, with familiarity with GMP documentation and ALCOA principles, and hands-on