At a Glance
- Tasks: Lead quality initiatives and ensure compliance in a dynamic manufacturing environment.
- Company: Join a global leader in hygiene, health, and nutrition with a strong purpose.
- Benefits: Enjoy competitive pay, wellness support, and opportunities for professional growth.
- Why this job: Make a real impact on product quality and consumer safety in a collaborative team.
- Qualifications: Experience in pharmaceutical manufacturing and strong leadership skills required.
- Other info: Diverse workplace with a focus on inclusion and personal development.
The predicted salary is between 50000 - 65000 £ per year.
Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.
In Research and Development, we’re full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals – all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you’ll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
Location: Hull, HU8 7DS
We are looking for a Qualified Person (QP) to join our Quality Leadership Team as a strong quality leader. In addition to performing batch certification and release activities, you’ll work closely with cross‑functional teams to oversee a variety of GxP activities in our non‑sterile manufacturing facility to maintain compliance to GMP and drive continuous improvement. You will work with the Quality and Site Leadership teams to support the execution of the QMS and ongoing maintenance of the MIA, whilst delivering quality improvement initiatives. The role is proactive in identifying, communicating, and mitigating quality and compliance risks and driving continuous improvement.
Your responsibilities:
- Member of the site Quality leadership team, influencing the site's quality strategy and priorities.
- QP certification and release of finished product batches produced at the Hull site.
- Ensuring regulatory and corporate GMP requirements are maintained for all factory activities.
- Facilitate the identification, communication and the ongoing removal of identified quality and compliance risks.
- Communication to Site Lead/Operations Manager, Site Quality Director and other key function heads as appropriate.
- Provide instruction and support on guidance to all areas of the site on GxP to ensure compliance with UK and any required International GxP Regulations and Guidelines.
- Communication and cascade of performance indicators identifying outstanding risks to key stakeholders.
- Interact with the Reckitt quality system to ensure change controls, quality event investigations and CAPAs are raised, managed, and closed out in line with company expectations.
- Providing support and leadership during regulatory inspections, maintain manufacturing authorisations and implement changes in legislation and regulatory guidance to ensure the ongoing compliance of the QMS.
The experience we're looking for:
- Eligible to undertake the duties of a Qualified Person as defined in SI 2012-1916 and Directive 2001/83/EC.
- Thorough knowledge of the legal requirements, rules and guidance covering the manufacture of pharmaceutical products.
- Experience in pharmaceutical manufacturing of non‑sterile dosage forms.
- Demonstrated experience in risk management, change management and validation.
- Experience of hosting Health Authority inspections.
- Highly developed leadership, critical thinking, communication, interpersonal, influencing and negotiating skills.
- Innovative and able to identify new approaches and ways of working.
- Strong planning, organisational and data analysis/interpretation skills.
- Familiar with modern business management techniques, methodology and tools.
- A positive willing and reliable attitude, providing good customer service to internal and external customers.
- Attention to detail and accuracy, strong time management skills, ability to work in a fast‑paced environment.
- Confidence, drive and ambition to make an impact on the business.
What we offer:
With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. 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.
Equality:
We recognise that in real life, great people don’t always ‘tick all the boxes’. That’s why we hire for potential as well as experience. Even if you don’t meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.
Qualified Person (QP) - Quality Manager employer: Reckitt Benckiser LLC
Contact Detail:
Reckitt Benckiser LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP) - Quality Manager
✨Tip Number 1
Network like a pro! Reach out to current employees on LinkedIn or at industry events. Ask them about their experiences and any tips they might have for getting your foot in the door.
✨Tip Number 2
Prepare for interviews by researching the company’s values and recent projects. Show how your skills align with their mission to create a cleaner, healthier world. We want to see your passion!
✨Tip Number 3
Practice your responses to common interview questions, especially around quality management and compliance. We love candidates who can articulate their experience clearly and confidently.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team.
We think you need these skills to ace Qualified Person (QP) - Quality Manager
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience and skills that align with the Qualified Person role. We want to see how your background fits into our mission of creating a cleaner, healthier world.
Showcase Your Leadership Skills: As a key player in our Quality Leadership Team, it’s important to demonstrate your leadership abilities. Share examples of how you've influenced quality strategies or led teams in previous roles to show us you’re the right fit.
Be Clear and Concise: When writing your application, keep it straightforward and to the point. We appreciate clarity, so make sure your achievements and experiences are easy to read and understand. This helps us see your potential quickly!
Apply Through Our Website: We encourage you to submit your application through our website. It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Reckitt Benckiser LLC
✨Know Your Regulations
Make sure you brush up on the legal requirements and guidelines surrounding pharmaceutical manufacturing, especially those related to GxP. Being able to discuss these confidently will show that you’re not just familiar with the role but also committed to maintaining compliance.
✨Showcase Your Leadership Skills
As a Qualified Person, you'll be part of the Quality Leadership Team. Prepare examples of how you've influenced quality strategies in previous roles. Highlight your experience in risk management and how you've led teams through challenges—this will demonstrate your capability to drive continuous improvement.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific quality or compliance risks. Think about past experiences where you identified and mitigated risks, and be ready to explain your thought process. This will help interviewers see your critical thinking and problem-solving skills in action.
✨Communicate Effectively
Strong communication is key in this role. Practice articulating complex ideas clearly and concisely. Be prepared to discuss how you’ve communicated performance indicators and risks to stakeholders in the past, as this will highlight your interpersonal skills and ability to influence others.