Job Summary:
As a Senior Equipment Specialist, you will be responsible for managing the successful introduction and qualification of equipment and systems in our QC Analytical workstream. This role requires excellent planning, organizational, and communication skills to ensure timely delivery of tasks as per project schedules.
Key Responsibilities:
• Act as lead for Equipment and System Introduction and Qualification within the team.
• Ensure compliance with EudraLex GMP guidelines and applicable regulatory requirements.
• Manage QC Equipment Specialists and ownership of QC Equipment and Systems within QC.
• Provide effective communication and lead project management interactions with internal and external clients.
Requirements:
• 4+ years experience working in a fast-paced environment.
• Experience in a GMP facility, preferably in a lead or project management role.
• Excellent computer skills, including MS Office (Word, Excel, PowerPoint).
• Strong knowledge and experience in validation or qualification of laboratory instrumentation, ideally within a pharma/biopharma FDA regulated environment.
Benefits:
• Bonus
• Canteen
• Life Assurance
• Paid Holidays
• Parking
• Pension
• VHI