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Senior Associate Scientist (Technical Services)

Location: Cork
Experience:4-5 Years
Job Type:Permanent
Salary:Not Disclosed
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Our client is a leading Biopharma, based in Cork. They are seeking an Associate Scientist for their technical Services team. The ideal person shall have a strong GMP background with 5+ years experience.


  • Leads technical support activities related to maintaining commercial product supplies through management of internal and external resources.
  • Contributes to and leads complex processes across functions and interacts effectively with the other team members to ensure product meets regulatory, performance, and cost requirements.
  • Contributes to and leads technical investigations of process deviations, and assessment of their impact on product quality. Defines requirements for, and reviews master batch records.
  • Contributes to user requirement specification and provides expert process technical support to utilize and validate new and improved technologies.
  • Liaises with manufacturing groups to deliver new and improved drug products and processes.
  • Can lead one or more specific components of departmental strategic initiatives.
  • Revises, improves or develops new methods to support commercial products; writes protocols and reports.
  • Assists with bench experiments to support collaborations with external researchers
  • Identifies and introduces new technology and/or methods to the organization, and trains junior staff on their implementation.
  • Analyzes and identifies risks with processes, technologies and methods, creates a working plan to prevent potential issues.
  • Designs experiments and ensures they accomplish goals.
  • Identifies opportunities to improve processes within the business and provides technical expertise and support to process improvement efforts.
  • May supervise personnel, including organizing and prioritizing daily tasks, and performing training.


  • 5+ years relevant GMP experience and a BS degree or MS degree in a relevant scientific discipline.
  • Or fundamental relevant experience and a PhD degree in a relevant scientific discipline.
  • Demonstrates a working knowledge of regulatory filing requirements and guidance documents (i.e. SUPAC, PACPAC).
  • Demonstrates excellent verbal, written, and interpersonal communication skills.
  • Demonstrates strong computer, organizational, and project management skills.

For further details plesae contact Karen Shiel at 087 7452487 or send CV to


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