Doc Controller

Desired Skills: MS Office Suite,Doc control,Tech Writing,Compliance,Science,Engineering

The Role

PE Global are recruiting for a Senior Document Controller for our biopharmaceutical client based in Dublin 15. This is an initial 12 -month contract role.

Job Responsibilities

• Client-side control of all project documentation across the full lifecycle
• Manage document receipt, review, approval, issue, revision control and archiving
• Interface with EPCM partners, vendors, contractors and internal stakeholders
• Ensure documentation complies with GMP, data integrity and ALCOA+ principles
• Maintain accurate document registers, trackers and status report
• Support CQV documentation, executed protocols and final turnover to operations
• Support audits, inspections and project close-out activities

Educations & Experience

• Bachelors degree in Science/Engineering
• Proven experience as a Document Controller on pharmaceutical or life sciences capital projects
• Essential: hands-on experience using EIDA for document management
• Experience working client-side or within an owner’s project team
• Strong understanding of GMP documentation requirements
• Experience supporting construction, commissioning and qualification documentation
• Experience on large-scale Irish pharma projects (drug product, biologics, sterile facilities)
• Familiarity with ValGenesis, Kneat, ACC or similar platforms

Interested candidates should submit an updated CV.

Please click the link below to apply, or alternatively send an up-to-date CV to aisling.oleary@peglobal.net

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland****