At a Glance
- Tasks: Lead the Quality Assurance function in a dynamic pharmaceutical manufacturing environment.
- Company: Established pharmaceutical manufacturer with a focus on Oral Solid Dose production.
- Benefits: Competitive salary, comprehensive benefits, and a strategic leadership role.
- Other info: Join a collaborative team and drive continuous improvement in a highly regulated setting.
- Why this job: Make a significant impact on quality culture and regulatory compliance in a vital industry.
- Qualifications: Degree in relevant scientific discipline and extensive QA leadership experience.
The predicted salary is between 80000 - 100000 £ per year.
An established pharmaceutical manufacturer is seeking a Director of Quality Assurance to lead the QA function across a complex Oral Solid Dose (OSD) manufacturing operation. This is a strategic leadership position responsible for driving quality culture, regulatory compliance, inspection readiness, and continuous improvement while partnering with Manufacturing, Supply Chain, Technical Operations and senior site leadership.
The successful candidate will provide direction to multiple QA teams, ensuring products are manufactured in accordance with GMP requirements and global regulatory expectations.
Key Responsibilities- Provide strategic leadership for the site Quality Assurance function across OSD manufacturing operations.
- Lead and develop multiple QA teams, fostering a strong quality culture and high-performance environment.
- Ensure ongoing compliance with EU GMP, FDA and other applicable regulatory requirements.
- Maintain inspection readiness and lead regulatory inspections from agencies including FDA, MHRA and EMA.
- Oversee batch disposition processes and ensure robust quality decision-making.
- Drive continuous improvement initiatives across Quality Systems and manufacturing processes.
- Provide oversight of deviations, CAPAs, change controls, investigations and risk management activities.
- Partner closely with Manufacturing, MS&T, Engineering, Validation, QC and Supply Chain to support operational excellence.
- Review quality metrics and identify trends to proactively improve performance.
- Ensure effective implementation and maintenance of the site's Quality Management System (QMS).
- Support new product introductions, technology transfers and commercial manufacturing activities.
- Manage quality-related risks and ensure appropriate governance across the site.
- Act as a key member of the site leadership team, influencing business strategy from a quality perspective.
- Degree in Pharmacy, Chemistry, Pharmaceutical Sciences or another relevant scientific discipline.
- Extensive Quality Assurance leadership experience within a GMP-regulated pharmaceutical manufacturing environment.
- Significant experience supporting Oral Solid Dose (OSD) manufacturing.
- Strong working knowledge of EU GMP, FDA regulations, ICH guidelines and global quality standards.
- Demonstrated experience leading regulatory inspections and managing audit responses.
- Proven ability to lead large multidisciplinary QA teams.
- Experience working with complex manufacturing operations and cross-functional stakeholders.
- Strong leadership, communication and stakeholder management skills.
- Strategic mindset with the ability to balance quality, compliance and business objectives.
- Experience within a multinational pharmaceutical manufacturing environment.
- Exposure to new product introduction (NPI), technology transfer or site expansion programmes.
- Knowledge of digital quality systems and continuous improvement methodologies (Lean/Six Sigma).
- Senior leadership opportunity within a highly regulated pharmaceutical manufacturing site.
- Strategic role with significant influence across site operations.
- Opportunity to lead a well-established Quality organisation supporting complex OSD manufacturing.
- Competitive salary and comprehensive benefits package.
Director of Quality Assurance in England employer: Thor
Join an esteemed pharmaceutical manufacturer as the Director of Quality Assurance, where you will lead a dynamic QA function in a collaborative and innovative environment. With a strong commitment to quality culture and regulatory compliance, this role offers significant opportunities for professional growth and influence within a highly regulated industry. Enjoy a competitive salary, comprehensive benefits, and the flexibility of a hybrid work model, all while contributing to the advancement of Oral Solid Dose manufacturing.
StudySmarter Expert Advice🤫
We think this is how you could land Director of Quality Assurance in England
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Thor. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Thor.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Thor. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
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 Thor is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Director of Quality Assurance in England
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 Thor!
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 Thor 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 Thor!
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 Thor, 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 Thor
✨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 Thor that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
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
Take some time to familiarise yourself with Thor’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
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.
