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- Tasks: Ensure quality management and compliance in a cutting-edge cannabis production facility.
- Company: Join a dynamic startup focused on high-quality, UK-produced cannabis medicines.
- Benefits: Competitive salary, hands-on experience, and growth in a fast-paced environment.
- Why this job: Be part of an innovative team making a real difference in patient care.
- Qualifications: Experience in GxP environments and a relevant degree required.
- Other info: Must be a strong communicator and own a car for site travel.
The predicted salary is between 36000 - 60000 £ per year.
Cpl Life Sciences is collaborating with a growing organisation that meets patient demand for a dependable supply of high quality, UK produced, cannabis-based medicines. The business operates a brand-new state of the art growing facility, processing environment, and laboratory.
Primary responsibilities:
- Ensuring the maintenance and inspection readiness of our GMP quality management system
- Managing Quality Events such as deviations, CAPAs, and change controls
- Managing the GACP QMS
- Assisting with Home Office licensing compliance where required
- Writing, updating and reviewing records, SOPs, and other documents
- Working with the Production Manager and the Quality Control Manager to ensure compliance with the QMS and Good Documentation Practice
- Track and ensure compliance with SOP review cycles and training
- Quality Event Management:
- Identifying and raising deviations
- Leading root cause analysis
- Generating and implementing CAPA plans
- Change management and post-implementation review
- Tracking QE metrics and reporting them to the business
- Oversee the approval of Customers and Suppliers
- Where required, communicate and work with the external supplier's QA functions
- Working closely and communicating effectively with the Growing, Production, Quality Control and Commercial functions to ensure the product is released safely and efficiently
- Assisting with Home Office licensing compliance where required
Desired Qualifications and Experience:
- Experience in a GxP environment
- Management of a QMS and quality events
- Relevant degree
This role is working for a startup organisation, so you must be a strong communicator who is dynamic and able to pick up things quickly. Due to the nature of the work, this will be on site, and you must own your own car to travel to the site. The working hours are 8am till 5pm and it is a 42hr week.
QA Associate employer: CPL
Contact Detail:
CPL Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Associate
✨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 that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP and QMS. We want you to show off your expertise! Practise common interview questions and think about how your experience aligns with the role of a QA Associate.
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can keep you fresh in their minds. It shows you're genuinely interested in the position and helps build a connection.
✨Tip Number 4
Apply through our website! We make it super easy for you to find and apply for roles that match your skills. Plus, it’s a great way to ensure your application gets seen by the right people.
We think you need these skills to ace QA Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QA Associate role. Highlight your experience in GxP environments and any relevant qualifications. We want to see how your skills match what we're looking for!
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 mission. Keep it concise but impactful – we love a good story!
Showcase Your Communication Skills: Since this role involves working closely with various teams, make sure to highlight your communication skills in your application. We value strong communicators who can collaborate effectively across departments.
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 – just a few clicks and you’re done!
How to prepare for a job interview at CPL
✨Know Your GMP Basics
Make sure you brush up on Good Manufacturing Practice (GMP) principles before the interview. Understanding how these regulations apply to quality management systems will show that you're serious about the role and can hit the ground running.
✨Prepare for Quality Event Scenarios
Think of examples from your past experience where you've managed quality events like deviations or CAPAs. Be ready to discuss how you identified issues, led root cause analyses, and implemented corrective actions. This will demonstrate your hands-on experience in a GxP environment.
✨Show Off Your Communication Skills
Since this role requires effective communication with various teams, prepare to discuss how you've successfully collaborated with different departments in the past. Highlight any experiences where your communication made a significant impact on project outcomes.
✨Stay Updated on Regulatory Requirements
Familiarise yourself with the latest regulatory requirements related to cannabis-based medicines and quality assurance. Being knowledgeable about current regulations will not only impress your interviewers but also show that you're proactive and committed to compliance.
