Compliance and Validation Manager
1 month ago
At Reckitt, we're committed to making access to high-quality hygiene, health, and nutrition a right, not a privilege. Our Manufacturing Excellence team is dedicated to improving the efficiency, quality, and safety of our manufacturing operations. We're seeking a Qualified Person (QP) to join our Quality Leadership Team as Compliance and Validation Manager.
Key Responsibilities:- Perform batch certification and release activities
- Oversee validation activities in our solid dose manufacturing facility
- Work with global Reckitt manufacturing sites and Third Parties to ensure quality oversight of validation activities
- Provide quality input and sign off of validation activity relating to facilities, equipment, and product transfers
As a member of our site Quality leadership team, you'll influence our quality strategy and priorities. You'll work closely with the Site Compliance Manager to ensure compliance with regulatory and corporate GMP requirements. You'll also be responsible for hosting regulatory inspections, maintaining manufacturing authorisations, and implementing changes in legislation and regulatory guidance.
We're looking for someone with a broad understanding of pharmaceutical manufacturing operations, business, and quality management systems. You'll need to have thorough knowledge of legal requirements, rules, and guidance covering the manufacture of pharmaceutical products. Experience in pharmaceutical manufacturing of solid dosage forms, risk management, change management, and validation is essential. You'll also need to be able to host Health Authority inspections.
We offer a range of benefits, including parental benefits, an Employee Assistance Program, and life insurance. We're committed to diversity and inclusion, and we welcome applications from all qualified candidates.
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