At a Glance
- 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 pharmaceutical safety and quality while being valued for your contributions.
- Qualifications: 2-4 years of QA experience in a GMP-regulated environment is essential.
- Other info: Gain exposure to diverse projects and clients in a supportive team.
The predicted salary is between 36000 - 60000 £ per year.
Senior QA Officer – Pharmaceutical Manufacturing – Wiltshire (On-site)
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:
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2-4 years of QA experience within a GMP-regulated pharmaceutical environment
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Strong working knowledge of GMP and pharmaceutical quality systems
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Experience working cross-functionally with QA/QC and operational teams
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Confident in coaching, training, and supporting junior staff
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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.
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Senior QA Officer employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QA Officer
✨Tip Number 1
Familiarise yourself with the specific GMP regulations and quality systems relevant to the pharmaceutical industry. This knowledge will not only help you in 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 industry peers can provide valuable insights and may even lead to referrals for the position.
✨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 results will resonate well with the hiring team.
✨Tip Number 4
Showcase your coaching and mentoring experience during discussions. Being able to illustrate how you've supported junior staff will align perfectly with the expectations of this role and demonstrate your leadership potential.
We think you need these skills to ace Senior QA 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 quality assurance and continuous improvement. Mention specific examples of how you've coached or supported junior staff and contributed to audit readiness in previous roles.
Highlight Relevant Skills: Clearly outline your skills that align with the job description, such as your proactive mindset and ability to drive compliance. Use keywords from the job posting to ensure your application stands out.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. A polished application reflects your attention to detail, which is crucial in a 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 the 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 Skills
As you'll be expected to coach and support junior team members, think of examples where you've trained or mentored others. Highlight your approach to fostering a supportive learning environment.
✨Express Your Passion for Continuous Improvement
The company values a proactive mindset, so come prepared with ideas on how you can contribute to continuous improvement initiatives. Discuss any past experiences where you've implemented changes that enhanced quality or efficiency.