This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
We’re building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. At CVS Health®, you’ll be surrounded by passionate colleagues who care deeply, innovate with purpose, hold ourselves accountable and prioritize safety and quality in everything we do. Join us and be part of something bigger – helping to simplify health care one person, one family and one community at a time. Cordavis is a wholly owned subsidiary of CVS Health. Cordavis makes strategic investments to bring pharmaceutical products to the U.S. market to increase competition and lower costs. Cordavis partners with manufacturers and payors to deliver: Sustainable cost savings for payors and patients. A reliable and predictable supply chain that minimizes disruption for patients. A responsible and viable long-term approach to deliver value and affordable products. Our partnerships create a vibrant and competitive marketplace, allowing us to expand our investments in future products to shape tomorrow's health care, today.
Job Responsibility:
Ensuring that the operations do not compromise the quality of medicines by ensuring that appropriate systems are in place throughout the supply chain
Ensuring that the conditions and authorized activities of the WDA and GDP guidelines are being followed and adhered to
Interaction with Health Products Regulatory Authority (HPRA) in relation to licence application and on-going maintenance of Wholesale Distribution Authorisation (WDA)
Ensuring that the Pharmaceutical Quality System (PQS) is implemented and maintained in compliance with GDP requirements
Approval of all GDP related procedures
Oversight of the approval of all GDP related suppliers and customers
Ensuring that any GDP deviations/non-conformances are fully investigated
Oversight of change control proposals
Lead inspection readiness activities
Preparation for, participation in and follow up on inspections
Ensuring that relevant customer complaints are handled appropriately
Oversight and approval of any decision to recall product
Involvement in any decision to quarantine or dispose of returned or rejected products
Approving any returns to saleable stock
Ensuring self-inspections are performed
Ensuring that relevant GDP personnel are trained
Leading the annual Quality Management Review
Review of performance metrics for suppliers
Ensuring Quality Agreements are in place
Oversight of the management, storage and control of quality records
Ensuring that any additional requirements imposed on certain products are adhered to
Maintaining records of any RP delegated duties
Requirements:
Minimum of a Bachelors’ degree, ideally in a bio-chemistry, life sciences, or microbiology related field
Advanced degree will be given preference, however, extensive industry experience acceptable in lieu of advanced degree