Site Quality Manager RB NL Brands B.V.

Join Reckitt's R&D organisation, where you will help ensure the quality, compliance, and onward supply of medicinal products across Europe as Site Quality Manager RB NL Brands B.V..

In Research and Development, highly skilled Scientists, Engineers, Medical, Clinical and Regulatory professionals work to create a cleaner, healthier world. The team focuses on developing and enhancing the portfolio without compromising on quality or performance.

Quality and integrity are central to the function, ensuring products are safe for consumers, meet the highest standards, and comply with regulatory legislation across the globe.

The size of the organisation offers opportunities to learn and work across different functions within R&D, with exposure to different disciplines, teams and environments. You will also have access to the Research and Development Academy to support your growth.

About the role

This role is responsible for Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) compliance of the Reckitt Benckiser ENA B.V. and RBNL Brands B.V. sites. This role will ensure the Quality Management Systems are implemented and maintained, ensuring the compliance of medicinal products imported into the EU for onward supply.

This role is responsible for the activities relating to operational quality for the EU Supply of medicinal products.

You will take accountability for the legal and routine duties of the QP role and therefore need to be eligible to be named as Qualified Person on the Manufacturing Importation Authorisation (MIA). You will take accountability for the legal and routine duties of the RP role and therefore need to be eligible to be named as Responsible Person on the Wholesale Distribution Authorisation (WDA).

You will form strong working relationships with the Reckitt Nottingham and Hull sites, the UK QPs, the UK RPs, the EU Supply Services and Commercial Quality teams to ensure the effective onward supply of medicines across Europe.

A strong working knowledge of EU GMP/GDP, the ability to communicate proactively, influence with impact, clearly and concisely both internally and externally are key to this role.

Your responsibilities

• Lead all Quality activities for the ENA BV Core Hub, including full ownership of the QMS, maintenance of MIA/WDA, Quality KPIs, documentation governance, and oversight of product complaints and recalls.
• Manage and develop the Quality Assurance team (three direct reports), ensuring GMP/GDP compliance, batch certification readiness, and effective training programmes across ENA BV.
• Act as QP and RP, ensuring all activities meet EU GMP/GDP requirements, national legislation, and MA expectations — including batch certification, safety features, supplier approvals, self-inspections, and recall execution.
• Partner cross-functionally with Supply, Finance, Tax, IT&D, Legal, Regulatory, R&D, Medical and Procurement to ensure compliant supply routes, NPD/EPD readiness, and robust CEP investigations and audit support.
• Drive continuous improvement, analysing KPIs, leading Quality Improvement Projects, managing risk assessments, adopting new technologies, and ensuring strong governance over subcontracted and GDP-relevant activities.

The experience we're looking for

• Qualified and experienced QP/RP with at least 3 years of practical QP experience in the EU, a scientific degree, and eligibility to act as QP/RP under EU/NL legislation; minimum 8 years in the Healthcare/Pharma environment.
• Strong GMP/GDP expertise, including deep understanding of EU and Dutch regulatory frameworks and requirements for products supplied from third countries (e.g., UK, Thailand).
• Proven leadership and partnership capabilities, able to work effectively across functions, influence at all levels, and facilitate alignment in a complex organisation.
• Strategic thinker with excellent execution skills, capable of turning strategy into actionable plans, managing multiple priorities, and maintaining a calm, logical, structured approach.
• Excellent communicator, with strong presentation skills and Quality Assurance experience (policies, procedures, audits, deviations, change control, CAPA), and the ability to build strong relationships internally and externally.

The skills for success

• Strategic Quality Leadership
• Regulatory & Compliance Expertise
• Operational Excellence & Continuous Improvement
• Effective People Leadership
• Cross-Functional Collaboration
• Risk Management & Decision-Making
• Investigation & Problem-Solving Skills
• Audit & Inspection Readiness
• Strong Communication & Stakeholder Management
• Project Management Capabilities

What we offer

We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.

We recognise that great people do not always tick every box. If this role and our company feel like a good fit, we still encourage interest from candidates who may not meet every requirement.