At a Glance
- Tasks: Manage quality systems, conduct audits, and ensure compliance in a dynamic environment.
- Company: Leading UK manufacturer of cannabis-based medicines with a sustainability focus.
- Benefits: Competitive salary, hands-on experience, and opportunities for professional growth.
- Why this job: Join a pioneering company making a real difference in patient care and sustainability.
- Qualifications: Relevant scientific degree or equivalent experience in a GMP production environment.
- Other info: Dynamic workplace with training support and career advancement opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Location: Wiltshire (on‐site)
The Opportunity
We are 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 is carbon‐negative by design and is scaling to meet growing patient demand.
What you will 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.
- Comfortable working in a dynamic, change‐driven setting.
- 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.
QA Associate in London employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Associate in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by practising common questions related to QA and GMP. We recommend doing mock interviews with friends or using online resources to get comfortable with your responses.
✨Tip Number 3
Showcase your passion for quality assurance! During interviews, share specific examples of how you've contributed to quality improvements in past roles. This will help you stand out as a candidate who truly cares about the field.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take that extra step to engage with us directly.
We think you need these skills to ace QA Associate in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QA Associate role. Highlight your experience in GMP environments and any relevant qualifications. We want to see how your background fits with what we’re doing at StudySmarter!
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 engaging and personal – we love a good story!
Showcase Your Skills: Don’t forget to showcase your skills related to quality management systems and compliance. Mention any specific tools or methodologies you’ve used, as this will help us see how you can hit the ground running in our dynamic environment.
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing applications come directly from our site!
How to prepare for a job interview at SRG
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practice (GMP) principles before the interview. Familiarise yourself with the specific regulations and standards that apply to the cannabis-based medicines sector, as this will show your potential employer that you're serious about quality assurance.
✨Prepare for Scenario Questions
Expect to be asked about how you would handle specific quality events or deviations. Think of examples from your past experience where you've successfully identified issues, led root cause analyses, or implemented corrective actions. This will demonstrate your problem-solving skills and your ability to drive inspection readiness.
✨Show Your Passion for Sustainability
Since the company is focused on sustainability, be ready to discuss your views on environmentally friendly practices in the pharmaceutical industry. Share any relevant experiences or ideas you have about how quality assurance can align with sustainability goals, which will resonate well with their mission.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions. Inquire about their current challenges in maintaining compliance or how they approach training for new SOPs. This shows your genuine interest in the role and helps you gauge if the company culture aligns with your values.