Description
QAV Specialist required to join a biotech company in Dublin for an initial 12 month contract. This CSV-focussed QAV Engineer will serve as the reviewer and approver on project milestones and documentation such as templates, risk assessments, commissioning, qualification, and validation activities. This person will serve as the QAV team member for the CSV team.Key Responsibilities:
* Collaborate with cross functional team to deliver project deliverables on time, on budget, and with Quality requirements being met
* Review and edit project documentation ensuring that Quality requirements are met
* Provide QAV approval on finalized project documentation
* Contribute to equipment and process risk assessments
* Provide QAV oversight for equipment qualification and commissioning activities including but not limited to factory acceptance testing and site acceptance testing
* Evaluate validation protocol content and execution
* Is a champion for safe working practices and safety initiatives within their area
Qualifications:
* University degree. Engineering or Science related discipline preferred
* Significant experience (10yrs +) working in the pharmaceutical or biotechnology industry
* Excellent written and verbal communication skills
* Experience working with dynamic cross-functional teams and influencing decisions
If this is you please apply today.