At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, ACO®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to a blended-branded business to win in self-care.

DESCRIPTION OVERVIEW

We are looking for a Analyst Quality Systems & Compliance Associate. We offer a Hybrid working schedule, a mix of onsite and remote working each week.

EXPERIENCE REQUIRED

• Scientific background with 2-3 years of experience in a pharmaceutical or medical devices company
• Ideally, 1-2 years in quality assuranc
• Good knowledge of ISO13485 and MDR
• Good IT knowledge and skills
• Self-starter, capable of working autonomously at corporate level
• Clear communicator, practical and solution orientated
• Enthusiastic and get the job done
• Strong project management skills & team worker in a multicultural environment
• Persistent drive for results in a fast-paced environment, utilizing sound project focus, organizational and problem solving skills
• You speak and write fluently English; other languages are an asset
• An innovative frame of mind – open to applying creative techniques to find a solution

The Quality Assurance Associate is in charge of Perrigo Medical Devices products for:

• CMO Management: responsible for all QA activities associated with the management of the CMOs under his/her responsibility.
• Product Quality Management: responsible for all QA activities related to the products under his/her responsibility associated with the development of new products, manufacturing line transfers, stability studies and validation activities.
• Technical File redaction: responsible for the preparation of the Manufacturing, Quality and stability sections of the technical files related to the products under his/her responsibility
• Support the maintenance of the Quality Management System: ensure that the SOP and templates used in daily activities are up to date and compliant with the relevant standards. Works according to PERRIGO QMS.
• Coordinate operational activities: collaborating with all the relevant stakeholders, the Quality Assurance Specialist ensures that Perrigo products are at any time compliant with the relevant regulation and standards. He/She provides QA expertise to all departments.