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- Tasks: Lead daily quality assurance activities and support the QA Manager in a hands-on role.
- Company: Join a rapidly growing pharmaceutical CDMO focused on innovation and quality.
- Benefits: Enjoy a collaborative environment with opportunities for growth and development.
- Why this job: Make a real impact on the safety and quality of pharmaceutical products.
- Qualifications: 2-4 years of QA experience in a GMP-regulated environment is essential.
- Other info: Gain exposure to diverse projects and clients while coaching junior team members.
The predicted salary is between 36000 - 60000 £ per year.
I am partnered exclusively with a well-established and rapidly growing pharmaceutical CDMO that continues to invest in innovation, quality, and expansion across the UK. This hire will play a key role in supporting the QA Manager by taking ownership of day-to-day quality assurance activities and contributing to the development of the wider QA function. You’ll be working closely with manufacturing and QC teams, helping to drive compliance, training, and continuous improvement across the site. This is a hands-on QA role where your experience in GMP environments will be essential. You’ll be expected to coach and support junior team members, contribute to audit readiness, and ensure that quality systems are maintained to the highest standards. If you’re looking for a role where your work directly impacts the safety and quality of pharmaceutical products – and where your contributions are visible and valued, this is a fantastic opportunity to grow within a collaborative, agile, and innovation-driven environment.
Key experience:
- 2-4 years of QA experience within a GMP-regulated pharmaceutical environment
- Strong working knowledge of GMP and pharmaceutical quality systems
- Experience working cross-functionally with QA/QC and operational teams
- Confident in coaching, training, and supporting junior staff
- A proactive mindset with a passion for continuous improvement
If you’re interested in joining a company where you’re not just a number and where you’ll gain exposure to a wide variety of projects and clients - please apply.
Senior Quality Assurance Officer employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Quality Assurance Officer
✨Tip Number 1
Familiarise yourself with the latest GMP regulations and quality systems in the pharmaceutical industry. This knowledge will not only help you during interviews but also demonstrate your commitment to maintaining high standards in quality assurance.
✨Tip Number 2
Network with professionals in the pharmaceutical QA field, especially those who have experience in CDMO environments. Engaging with them can provide insights into the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to continuous improvement initiatives in previous roles. Highlighting your proactive mindset and ability to coach junior staff will resonate well with the hiring team.
✨Tip Number 4
Research the company’s recent projects and innovations in the pharmaceutical sector. Being knowledgeable about their work will allow you to tailor your conversation during interviews and show genuine interest in their mission and values.
We think you need these skills to ace Senior Quality Assurance Officer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your 2-4 years of QA experience in a GMP-regulated pharmaceutical environment. Emphasise your knowledge of GMP and quality systems, as well as any relevant cross-functional work with QA/QC teams.
Craft a Compelling Cover Letter: In your cover letter, express your passion for continuous improvement and how your proactive mindset aligns with the company's values. Mention specific examples of how you've coached or supported junior staff in previous roles.
Highlight Relevant Skills: Clearly outline your skills related to compliance, training, and audit readiness. Use bullet points to make these stand out, ensuring they match the key experience mentioned in the job description.
Showcase Your Impact: Demonstrate how your contributions have directly impacted the safety and quality of pharmaceutical products in your past roles. Use quantifiable achievements where possible to illustrate your effectiveness in a hands-on QA role.
How to prepare for a job interview at RBW Consulting
✨Showcase Your GMP Knowledge
Make sure to highlight your experience in GMP-regulated environments during the interview. Be prepared to discuss specific examples of how you've ensured compliance and maintained quality systems in your previous roles.
✨Demonstrate Cross-Functional Collaboration
Since this role involves working closely with manufacturing and QC teams, be ready to share instances where you've successfully collaborated across departments. This will show your ability to work effectively in a team-oriented environment.
✨Emphasise Coaching Experience
As you'll be expected to coach and support junior team members, talk about your previous mentoring experiences. Highlight any training programmes you've led or contributed to, showcasing your leadership skills.
✨Express Your Passion for Continuous Improvement
Convey your proactive mindset by discussing initiatives you've taken to drive continuous improvement in your past roles. Share specific examples of how your contributions have positively impacted quality assurance processes.
