At a Glance
- Tasks: Lead quality and compliance for new product projects from concept to consumer.
- Company: Join Haleon, a purpose-driven consumer health company with bold ambitions.
- Benefits: Inclusive culture, career growth opportunities, and a chance to impact everyday health.
- Other info: Diverse and inclusive workplace committed to employee belonging and support.
- Why this job: Make a real difference in health products that millions trust and use daily.
- Qualifications: Bachelor’s degree in Pharmacy or Science; experience in Quality Assurance preferred.
The predicted salary is between 60000 - 75000 £ per year.
Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.
The purpose of this role is to manage the overall Quality and Compliance activities from initial concept to consumer for new product introduction and product lifecycle activities. As the R&D Quality representative, this role is an extended core team member and performs the Quality activities in support of the NPI & Maintenance projects. He/she is the single point of contact for Quality during the development, transfer and launch of new products and in addition lifecycle compliance management.
Key Responsibilities
- Lead the Quality / Compliance activities for new product projects, support from initial concept to consumer during the development and product transfer from R&D to site.
- Extended core Team Member of assigned projects and Quality liaison for project from initial concept to consumer. Accountable to ensure all functional Quality support is provided to the project.
- Review and approve project related documents, including product specification, batch documentation, test method, analytical validation report, method transfer, process and product transfer protocol and reports and packaging documentation. Also oversee Change Control, Deviation, and CAPAs for assigned projects.
- Support clinical supplies activities, including providing formal approval and release for clinical supplies, registration samples and consumer test supplies.
- Integration of customer and consumer insights effectively into NPI projects ensuring ongoing innovation and development addresses customer and consumer demands & perform Hypercare following launches.
- Provide leadership in the area of quality compliance. Quality partner to R&D and QSC, building and maintaining effective collaboration, detecting potential issues early, resolving product challenges swiftly, ensuring continuous improvement in our products' reliability, manufacturability, testing capabilities, and usability while maintaining compliance.
Knowledge/Education/Experience Required
- Bachelor’s Degree in Pharmacy, Science, OR equivalent level of knowledge, understanding and hands-on experience in a regulated environment.
- Previous experience in the pharmaceutical industry related to Quality Assurance, Drug Regulatory Affairs, Technical Operations, or Drug Development in a GMP environment.
- Manufacturing site experience.
Equal Opportunities
Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected – all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It’s important to us that Haleon is a place where all our employees feel they truly belong.
Adjustment or Accommodations Request
If you require a reasonable adjustment or accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific adjustments you are requesting. We’ll provide all reasonable adjustments to support you throughout the recruitment process and treat all information you provide us in confidence.
Note to candidates
The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.
R&D Quality Manager (FTC - 12 months) employer: Gsk
At Haleon, we pride ourselves on being a purpose-driven employer that champions everyday health through our renowned portfolio of brands. Our agile and performance-focused culture fosters collaboration and innovation, providing employees with ample opportunities for growth and development in a supportive environment. Located in a vibrant community, we are committed to inclusivity and ensuring that every team member feels valued and empowered to contribute to our mission of delivering better health with humanity.
StudySmarter Expert Advice🤫
We think this is how you could land R&D Quality Manager (FTC - 12 months)
✨Unlock Networking Opportunities
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When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Gsk is looking for. A tailored application can really make you stand out!
We think you need these skills to ace R&D Quality Manager (FTC - 12 months)
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Gsk!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Gsk that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Gsk!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Gsk, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Gsk
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Gsk that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
