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- Tasks: Lead R&D vendor audits and ensure compliance with global quality standards.
- Company: Join a leading global company focused on innovation and quality.
- Benefits: Competitive salary, professional development, and opportunities for global travel.
- Why this job: Make a real impact in the R&D field while ensuring product quality and compliance.
- Qualifications: Degree in a scientific discipline and experience in quality management required.
- Other info: Dynamic role with opportunities to collaborate globally and drive continuous improvement.
The predicted salary is between 36000 - 60000 £ per year.
The R&D Quality Manager Audit Lead leads the R&D vendor approval for the clinical and quality compliance pillar within the Europe Vendor Quality Team. The role manages all activities associated with the audit programme and related documentation for GxPs (GCP, GVP, GMP) within R&D. The audit team provides support to global R&D colleagues, providing SME audit support when required. The role may also be required to support supplier qualification and audit activities for the wider European Vendor Quality Team, Corporate Audits and release activities and related compliance activities for R&D Hull.
Responsibilities
- Management of External Compliance activities for R&D for all GxP and Core Reckitt products.
- Ability to collaborate with the global audit network to deliver the external audit programme and approve new vendors/ suppliers to R&D.
- Acts as an audit subject matter expert and support global R&D audit teams.
- Provide quality support for compliance activities including deviations, change controls and risk management relating to vendor quality management.
- Actively participates in quality culture and continuous improvement activities.
- Support the technology transfer process from R&D to commercial manufacture.
- Proactively monitors and responds to changes in guidance and legislation issued by Regulatory Authorities.
- Provides data and information to communicate supplier and supplier quality management performance at Quality Management reviews.
- Requires travel to global Reckitt sites and 3rd party vendors.
- Ensure data integrity compliance.
- Support and ensure GxP systems are compliant to global policy and procedures and regulatory standards.
Qualifications
- Trained and experienced lead auditor.
- Degree in a scientific discipline is required.
- Experience of working in a Quality environment for product development is essential.
- An appreciation and understanding of global medicines regulations is required.
- Previous line management experience is required.
- Ability to work cross functionally with global R&D teams and form collaborative relationships.
- Experience across a broad range of therapeutic areas and product classifications is desired.
- Ability to critically apprise Quality impacting regulatory guidance and legislation for internal action.
- Strong project management and organisational skills.
The skills for success: Commercial Awareness, Business Partnership, Collaboration, Partnership building, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Collaborator, R&D, Product Lifecycle Management.
R&D Quality Manager, Compliance - 12 Month Fixed Term Contract in Kingston upon Hull employer: Reckitt Benckiser Group plc.
Contact Detail:
Reckitt Benckiser Group plc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land R&D Quality Manager, Compliance - 12 Month Fixed Term Contract in Kingston upon Hull
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, especially those who work at Reckitt or similar companies. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of GxP regulations and compliance. We want you to be the go-to person for any questions they throw your way, so show off that expertise!
✨Tip Number 3
Don’t forget to showcase your collaboration skills! Highlight examples where you've worked cross-functionally or built partnerships. This role is all about teamwork, so let them know you’re a team player.
✨Tip Number 4
Finally, apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take that extra step to connect with us directly.
We think you need these skills to ace R&D Quality Manager, Compliance - 12 Month Fixed Term Contract in Kingston upon Hull
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the R&D Quality Manager role. Highlight your experience in compliance, auditing, and any relevant scientific qualifications to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality management in R&D and how your background makes you the perfect fit for our team. Keep it engaging and personal!
Showcase Your Collaboration Skills: Since this role involves working with global teams, emphasise your ability to collaborate and build partnerships. Share examples of how you've successfully worked cross-functionally in the past.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Reckitt Benckiser Group plc.
✨Know Your GxP Inside Out
Make sure you brush up on Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), and Good Manufacturing Practice (GMP). Being able to discuss these regulations confidently will show that you’re not just familiar with them, but that you can apply them in real-world scenarios.
✨Showcase Your Audit Experience
Prepare specific examples from your past experiences where you led audits or managed compliance activities. Highlight any challenges you faced and how you overcame them. This will demonstrate your expertise and ability to handle the responsibilities of the R&D Quality Manager role.
✨Emphasise Collaboration Skills
Since this role requires working cross-functionally with global teams, be ready to discuss how you've successfully collaborated in the past. Share stories that illustrate your ability to build partnerships and work effectively with diverse groups.
✨Stay Updated on Regulatory Changes
Research recent changes in regulatory guidance and legislation relevant to the role. Being able to discuss these changes and their implications during the interview will show that you’re proactive and committed to maintaining compliance in a dynamic environment.
