At a Glance
- Tasks: Lead a QA team, manage compliance, and oversee quality improvements in pharmaceutical manufacturing.
- Company: Join a leading pharmaceutical manufacturer focused on quality and employee development.
- Benefits: Enjoy competitive salary, permanent position, and opportunities for professional growth.
- Why this job: Shape the future of pharma with a supportive culture and hands-on leadership role.
- Qualifications: Experience in QA management, strong knowledge of GMP regulations, and a science degree preferred.
- Other info: Contact Gareth Gooley for a confidential chat about this exciting opportunity.
The predicted salary is between 36000 - 60000 £ per year.
Are you an experienced QA professional ready to take the next step in your career? Smart4 Sciences are working with a leading pharmaceutical manufacturing company in Northamptonshire that's on the lookout for a skilled QA Manager to join their growing team.
This is a fantastic opportunity to take ownership of the Quality Assurance function on a busy GMP site, support a collaborative and quality-driven culture, and help shape the future of pharmaceutical manufacturing.
The Role:
As QA Manager, you'll lead a small but experienced QA team and take responsibility for the site's QMS, GMP compliance, and internal audit programme. You'll work closely with production, QC, and supply chain teams to ensure products meet regulatory standards and are released efficiently, working alongside the QP.
This is a hands-on leadership role in a company that values continuous improvement and employee development.
What You'll Be Doing:
- Managing and mentoring the QA team
- Leading GMP compliance across manufacturing and packaging operations
- Owning and developing the Quality Management System
- Hosting and supporting audits (MHRA, client, internal)
- Overseeing deviations, CAPAs, change controls, and batch review
- Working cross-functionally to drive quality improvements
What We're Looking For:
- Solid QA background in pharmaceutical manufacturing
- Proven experience managing or leading a QA team
- Strong knowledge of EU GMP and GDP regulations
- Comfortable leading audits and interfacing with regulatory bodies
- A science degree (or equivalent experience) is preferred
Why Apply?
- Be part of a forward-thinking and supportive company
- Take ownership of quality strategy and improvements
- Enjoy a stable, permanent position with real development prospects
Interested? If you're a passionate QA professional looking for a new challenge in the Northamptonshire area, we'd love to hear from you. Apply today or contact Gareth Gooley for a confidential chat about the role.
QA Manager - Pharmaceuticals employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Manager - Pharmaceuticals
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who work in quality assurance. Attend industry events or join relevant online forums to connect with potential colleagues and learn about the latest trends and challenges in QA.
✨Tip Number 2
Familiarise yourself with the specific GMP regulations and standards that are relevant to the company you're applying to. This will not only help you in interviews but also demonstrate your commitment to understanding their operational environment.
✨Tip Number 3
Prepare to discuss your leadership style and experiences in managing QA teams. Think of specific examples where you've successfully led a team through challenges or implemented improvements in quality processes.
✨Tip Number 4
Research the company’s recent projects or initiatives in quality assurance. Being knowledgeable about their current focus areas can help you tailor your conversation during interviews and show that you’re genuinely interested in contributing to their goals.
We think you need these skills to ace QA Manager - Pharmaceuticals
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in QA within the pharmaceutical sector. Emphasise your leadership skills and any specific achievements related to GMP compliance and quality management systems.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance and your understanding of the pharmaceutical industry. Mention specific examples of how you've led teams or improved processes in previous roles.
Highlight Relevant Qualifications: Clearly state your educational background, especially if you have a science degree or equivalent experience. Include any certifications related to quality assurance or regulatory compliance that may set you apart.
Showcase Your Leadership Experience: In your application, provide examples of how you've managed or mentored QA teams. Discuss your approach to fostering a collaborative culture and driving continuous improvement within your team.
How to prepare for a job interview at Smart4Sciences
✨Showcase Your QA Expertise
Make sure to highlight your solid background in quality assurance within the pharmaceutical manufacturing sector. Be prepared to discuss specific examples of how you've managed or led QA teams and ensured compliance with EU GMP and GDP regulations.
✨Demonstrate Leadership Skills
As a QA Manager, you'll be leading a team, so it's crucial to convey your leadership style. Share experiences where you've successfully mentored team members or driven quality improvements, showcasing your ability to foster a collaborative and quality-driven culture.
✨Prepare for Audit Scenarios
Since hosting and supporting audits is a key part of the role, prepare to discuss your experience with audits, including MHRA and internal audits. Be ready to explain how you handle deviations, CAPAs, and change controls, as well as your approach to ensuring compliance.
✨Understand Cross-Functional Collaboration
The role requires working closely with production, QC, and supply chain teams. Be prepared to talk about how you've successfully collaborated across functions in the past to drive quality improvements and ensure products meet regulatory standards.