Biopharma Document Control Engineer (12-month Contract)

Claran Consultants Ltd; Cork; On-site; EUR 38,000 - 52,000; Full time

Job summary

Claran Consultants Ltd in Cork seeks an Engineering Document Control Specialist for a biopharma facility. You will report to the Core Projects Manager and oversee the control of the engineering documentation system.

This is initially a 12-month contract. Responsibilities include maintaining the Engineering Documentation Control Centre, drafting controlled documents with Veeva and Trackwise, and ensuring proper archiving and regulatory compliance.

Qualifications

• Bachelor's degree in a relevant technical field required.
• 1-2 years' GMP environment experience preferred.
• Strong written and verbal communication skills.

Responsibilities

• Control and maintenance of the Engineering Documentation Control Centre.
• Issue and archive project and site drawings.
• Manage numbering for commissioning and restart documents.
• Prepare and draft controlled documents using Veeva and Trackwise.
• Circulate project engineering transmittals and maintain registers.
• Ensure compliance for removal and archiving of documents.

Skills

GMP

Attention to detail

Verbal communication

Education

Bachelor's degree in a relevant technical field

Tools

Veeva

Trackwise

Job description

Claran Consultants Ltd in Cork seeks an Engineering Document Control Specialist for a biopharma facility. You will report to the Core Projects Manager and oversee the control of the engineering documentation system.

This is initially a 12-month contract. Responsibilities include maintaining the Engineering Documentation Control Centre, drafting controlled documents with Veeva and Trackwise, and ensuring proper archiving and regulatory compliance.