A rapidly expanding Biotech Manufacturing company based in Cork, is seeking to fill the position of Design, Qualification & Validation (DQV) Manager.
Key Responsibilities
* Management and execution of the Master Validation Schedule
* Management of product drawing execution and qualification
* Management of Sub-Supplier Component specification & Qualification
* Alignment of Customer User Requirement Specification and Compliance
* Collaborating extensively with the Engineering team in the continued development of both existing and new products introductions.
This role requires a strong background and keen interest in Quality, Validation and Project Management.
Requirements
* Educational Background: Degree in Process, Biotechnology, or related Engineering field.
* Experience: 8+ years' experience working in a GMP environment across Quality and / or Validation.
* Strong experience managing product lifecycles in a dynamic environment.
* Project management experience (lead out and delivery)
* Analytical and Strategic Thinking: Ability to assess and problem solve
* Communication Skills: Ability to communicate complex concepts clearly and effectively.
This individual will play a key role in the continued development and strategic direction of the business, driving innovation in the biopharma industry while collaborating across quality, engineering, and production teams.
About Us
{company} is a leading Biotech Manufacturing company based in Cork.