Description
Quality Manager required for a pharmaceutical Company based in Dublin with a minimum of 7 years experience in quality/supervisory/management within a bulk API manufacturing site environment. Responsible for managing and co-ordinating all site QA / QC and Regulatory Affairs activities..Responsibilities includes:
-Extensive knowledge / experience of effective implementation of all relevant cGMP guidelines and marketing authorisations, manufacturing site quality systems, customer and regulatory audits is required
-Management of the site quality systems to ensure that high quality product is delivered on time to customers on a consistent basis,
-oversight of the preparation for compliance audits,
-oversight and planning of QC activities in conjunction with Manufacturing and Sales Departments and ensuring all departments across the site comply with the relevant cGMP guidelines.
-Regular liaison with Group QA and Regulatory Affairs is required.
Requirements:
-Third level qualification in a Life Sciences discipline with a
-Minimum of 7 years experience in quality / supervisory / management roles on API manufacturing sites, ideally in both QC and QA roles.
-Excellent communication, presentation, time management and people management skills.
This is an exciting opportunity in a successful organisation with a highly competitive remuneration and benefits package on offer. If you are interested in this opportunity and would like to hear more about the role and company please contact me Anna Mooney or apply below with an up to date CV.