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- Tasks: Ensure quality standards in a cutting-edge cannabis medicine facility and manage quality events.
- Company: Innovative UK manufacturer focused on sustainability and patient care.
- Benefits: Competitive salary, training opportunities, and a chance to work in a unique industry.
- Why this job: Join a forward-thinking team and make a real difference in the healthcare sector.
- Qualifications: Relevant scientific degree and experience in GMP quality roles.
- Other info: Dynamic work environment with a commitment to sustainability and growth.
The predicted salary is between 36000 - 60000 ÂŁ per year.
We’re supporting a UK manufacturer of cannabis‑based medicines that has recently brought a new, state‑of‑the‑art growing, processing and lab facility online in the Southwest. The organisation runs a sustainability‑led operation that’s carbon‑negative by design and is scaling to meet growing patient demand.
You’ll report into the Head of Quality and help keep the site inspection‑ready by strengthening the Quality Management System (QMS), managing quality events, and collaborating across Production, QC, and Growing teams.
What you’ll be doing:
- Own core elements of the GMP QMS—write, update and review SOPs/records; ensure Good Documentation Practice; track SOP review cycles and training; and maintain complete, compliant records.
- Manage quality events—identify and raise deviations, lead root cause analysis, define and implement CAPAs, oversee change control and complete post‑implementation reviews, track metrics and report into the business.
- Drive inspection readiness—plan and run self‑inspections, conduct independent audits and risk assessments, and keep current with relevant regulatory requirements.
- Supplier & customer oversight—support approvals and liaise with external supplier QA where needed.
- Controlled drugs compliance—assist with Home Office licensing requirements as needed.
- Broader quality support—help maintain the GACP QMS alongside GMP activities.
About you:
- A relevant scientific or technical degree (or equivalent experience).
- Experience in a quality focused position within a GMP production environment.
- Experience of GMP QMS.
- Knowledge of GACP would be advantageous but training and support will be provided.
Please note – to be considered for this position you will need to pass an enhanced DBS Check.
Quality Assurance Associate in Hounslow employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Associate in Hounslow
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those working in quality assurance or related fields. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP QMS and relevant regulations. We recommend practising common interview questions and scenarios that might come up, so you can showcase your expertise confidently.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website for the best chance at landing the job! We keep our listings updated, and applying directly can sometimes give you an edge over other candidates.
We think you need these skills to ace Quality Assurance Associate in Hounslow
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Assurance Associate role. Highlight your experience in GMP environments and any relevant qualifications. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance and how you can contribute to our sustainability-led operation. Keep it concise but impactful.
Showcase Relevant Experience: When detailing your experience, focus on specific examples that demonstrate your knowledge of QMS and GMP practices. We love seeing how you've tackled challenges in previous roles!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at SRG
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practice (GMP) and Quality Management Systems (QMS). Be ready to discuss your previous experiences in these areas, as well as any specific SOPs you've worked with. This will show that you’re not just familiar with the concepts but can apply them effectively.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've identified quality events and led root cause analyses in past roles. Highlight your experience with CAPAs and how you’ve implemented changes based on your findings. This will demonstrate your proactive approach to quality assurance.
✨Stay Current with Regulations
Familiarise yourself with the latest regulatory requirements relevant to the cannabis-based medicine industry. Being able to discuss these during your interview will show that you’re serious about compliance and can help keep the organisation inspection-ready.
✨Collaborate and Communicate
Since the role involves working across various teams, think of examples where you’ve successfully collaborated with others. Be prepared to discuss how you’ve communicated quality issues and solutions to different stakeholders, as this is key in a quality assurance position.
