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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 cannabis-based medicines.
- Benefits: Competitive salary, hands-on experience, and growth in a unique industry.
- Why this job: Be part of an innovative team making a real difference in patient care.
- Qualifications: Experience in GxP environments and strong communication skills required.
- Other info: 100% on-site role with excellent career development opportunities.
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
Self-inspection
- Oversee self-inspections of the quality system and conduct independent audits and risk assessments for all relevant activities
- Maintain knowledge and understanding of regulatory requirements in relation to the role
Supplier Management
- Oversee the approval of Customers and Suppliers
- Where required, communicate and work with the external supplier's QA functions
Communication:
- Working closely and communicating effectively with the Growing, Production, Quality Control and Commercial functions to ensure the product is released safely and efficiently
Controlled Drugs
- 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 100% 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.
Quality Assurance Associate in Swindon employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Associate in Swindon
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their products and values, especially since they focus on cannabis-based medicines. Tailor your answers to show how you fit into their mission.
✨Tip Number 3
Practice common interview questions related to quality assurance and GMP compliance. We recommend doing mock interviews with friends or mentors to build confidence and refine your responses.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Quality Assurance Associate in Swindon
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Assurance 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 Life Sciences
✨Know Your GMP Basics
Make sure you brush up on Good Manufacturing Practices (GMP) before the interview. Understanding how these practices apply to cannabis-based medicines 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.
✨Familiarise Yourself with Regulatory Requirements
Research the regulatory landscape surrounding cannabis-based medicines and quality management systems. Being knowledgeable about compliance will not only impress your interviewers but also show that you're proactive and ready to tackle the challenges of the role.
