EXCELLENT BIOPHARMA OPPORTUNITY - We require a number of QA Specialist (12 month contract) for our Cork based trailblazing biopharma client. Calling all those with Pharma or Med Devices experience.
Join a leading multinational currently expanding their team today.
Role of this position
- Acts as the day-to-day QA project contact person for the Manufacturing and Engineering departments providing guidance / feedback on quality issues related to their respective area project activities.
- Completes the review/ approval of Manufacturing and Engineering project documentation - in particular equipment/ process/ automation validation documentation.
- Performs a wide variety of activities to ensure compliance with applicable regulatory requirements.
- Actively contributes to continuous improvement initiatives.
- Builds and maintains good working relationships with Engineering, Manufacturing and Quality department personnel in particular.
- B.Sc. in science/engineering in cGMP Quality environment.
Please call Michael Hanrahan today for further information on 021-2019817 or email: firstname.lastname@example.org
CareerWise Recruitment (In Search of Excellence)