Quality Assurance Analyst in Dodworth

Quality Assurance Analyst – 1 Year Fixed Term Contract

Join to apply for the Quality Assurance Analyst – 1 Year Fixed Term Contract role at Perrigo Company plc

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®, 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.

Scope of the Role

• Releases medicinal products to the market for the OPL business as RPi delegate. Ensuring product is safe for patients and any investigations are completed using risk‑based processes.
• Support quality systems on site for raising of Change Controls, Deviations, CAPAs as required, writing SOPs.
• Acts as Quality Lead on business projects.
• Oversee routine + ad hoc rework processes, approve BOMs and manage FSDU/Display Pack Projects.
• Manage the Periodic Quality Review programme, preparing the OPL QA reviews and ensuring schedule adherence.
• Supplier and Customer qualification and maintenance including annual bona tides and monthly GMDP compliance checks.
• Participation in the self‑inspections, internal and regulatory audits and ensuring necessary corrective actions are put in place.

Experience Required

• Scientific University Degree or equivalent
• Minimum of 5 years’ experience in a GDP Quality Assurance Role in the Pharmaceutical Industry.
• Good understanding of EU GDP/GMP
• Ability to maintain high quality documentation, manage data sources and interpret data for key Performance Indicators to judge the operational state of processes.
• Work independently on QMS elements they are responsible – knowing when to escal the appropriate any issues.
• Experience using electronic documentation systems e.g., Trackwise, SAP.
• Comprehensive understanding of GMP, GDP, regulatory (UK Human Medicines, MHRA) and broader EU / PICS/ISO requirements for pharmaceuticals, cosmetics, biocides, food supplements & medical devices together with experience direct experience of dealing with regulatory agencies on quality and compliance matters.
• Thorough knowledge of technical and commercial requirements of the business associated with the quality units\’ activities, role and resource. Acts as consulting expert in the quality field for complex issues associated with quality, technical and regulatory requirements for the business, especially as they relate to GDP.

Benefits

We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Hybrid Working Approach

We love our offices and the setting they provide for in‑person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo