GMP Documentation & QA Systems Specialist

Viatris; Galway; On-site; EUR 45,000 - 60,000; Full time

Benefits offered by this job

Health insurance

Pension

Bonus scheme

Work-life balance initiatives

Job summary

Viatris is seeking a Quality Assurance Documentation Controller to manage the site GMP documentation system and administer the My University training quality system for the QA team. The role involves coordinating document changes, issuing and archiving quality records, and supporting QA training with SMEs.

The ideal candidate holds a science degree, has meticulous attention to detail, strong communication skills, and experience with IT systems and MS Office; pharma experience is desirable but

Qualifications

• Bachelor's degree in a science-related field is required.
• Pharma/medical device experience is desirable but not essential.
• Excellent attention to detail and strong communication and interpersonal skills.
• Ability to manage multiple tasks in a fast-paced environment with good time management.
• Experience with IT systems and Microsoft Office is required.

Responsibilities

• Manage the site GMP documentation system on a day-to-day basis.
• Administer the My University training quality system for the QA team.
• Coordinate and review changes to quality documents prior to approval.
• Distribute new documents and retrieve old documents as needed.
• Archive quality records and assist in preparing, revising, and reviewing quality system records.
• Coordinate QA training with SMEs and manage material master data; report QA performance metrics.

Skills

Attention to detail

Communication

Interpersonal skills

Time management

Multi-tasking

IT systems

Microsoft Office

Electronic document management systems

Education

Bachelor's degree in a Science related discipline

Tools

Electronic document management systems

Job description

Viatris is seeking a Quality Assurance Documentation Controller to manage the site GMP documentation system and administer the My University training quality system for the QA team. The role involves coordinating document changes, issuing and archiving quality records, and supporting QA training with SMEs.

The ideal candidate holds a science degree, has meticulous attention to detail, strong communication skills, and experience with IT systems and MS Office; pharma experience is desirable but