Technical Writer
Industry : Pharmaceutical
Department: Technical Operations
Role Summary:
Pharmaceutical company has a requirement for a Technical Writer in their Technical Operations
Compliance department in Limerick.
As a Consultant Technical Writer, a typical day may include:
• Liaise with the Automation and Validation departments in an effective and timely manner as part of generating Automated System Periodic Evaluation Program (PER Program) reports.
• Responsible for generating maintenance reports as part of the Maintenance program example review and trending of work records. Liaise with multiple departments in data review. Collate responses in a timely and effective manner.
• Facilitate reviews and revisions of Department related SOP’s, life cycle documents, plans and policies for each group within the Department.
• Facilitate support of preventative maintenance record review and audit trail review.
• Ensure report writing deadlines are meet and data is concise and accurate and meets ALCOA+ principles.
• Support department in lead up to audit in preparation of support documentation.
• Support automation in administration of equipment access.
• Maintains knowledge of current good manufacturing practices (cGMPs).
This role will require the following:
• Experience working in a regulated GxP environment.
• Ability to work on own initiative, without direct supervision from management.
• Team player with an ability to work well across various departments on site as well as business partners.
• Project management skills.
• Excellent written and communication skills.
• Deadline focused individual.
Contract Duration: 12 Months
Location: Limerick