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- Tasks: Join us as a Validation Quality Engineer, ensuring our medical cannabis production meets GMP standards.
- Company: Be part of the only Scottish medical cannabis company with EU GMP certifications and domestic cultivation licenses.
- Benefits: Enjoy hybrid work options, competitive salary, pension, and free on-site parking.
- Why this job: Contribute to a pioneering company shaping the future of medical cannabis access in the UK.
- Qualifications: Must have 2+ years in validation within GMP-regulated pharmaceuticals or medical cannabis.
- Other info: Bonus points for QA experience and managing a QMS system.
The predicted salary is between 28000 - 42000 £ per year.
Validation Specialist (GMP) Pharmaceutical Industry / Medical Cannabis Dumfries & Galloway, Langholm, Scotland DG13 (Hybrid: 4 days on-site, 1 day remote)
Please only apply if you have experience with GMP in a Pharmaceutical company.
Founded in 2019, my client is the only Scottish & UK-based medical cannabis pharmaceutical company that holds both EU GMP certifications and licenses to cultivate medical cannabis domestically in the UK, whilst also holding the licences to import and distribute medical cannabis.
Over the past four years, they’ve built a brand-new, EU GMP-certified medical cannabis production facility in Scotland — including a large-scale, high-tech greenhouse. With all infrastructure and approvals now in place, they’re preparing to launch their first in-house cultivated and manufactured medical cannabis medicines into the UK market.
Since 2020, the business has taken a dual-track approach: building out its domestic cultivation and medical cannabis pharmaceutical production capabilities—including hiring a top-tier team, establishing R&D operations, implementing SOPs, and securing full Home Office and MHRA approvals—while simultaneously running an active medical cannabis importation and distribution operation.
This hybrid model ensures they can provide UK patients access to both internationally sourced and soon, UK-grown medical cannabis medicines.
With an experienced and senior Quality team of three already in place — including both an RP and a QP— they are now looking for a dedicated Validation Specialist to help them validate their GMP production facility, to enable internal manufacturing and production of medical cannabis. This is a critical role for a Validation Specialist with strong experience working in GMP-regulated pharmaceutical environments.
You will be responsible for planning, executing, and documenting validation activities for the company’s new medical cannabis production facility and cleanrooms. This includes facility, software, equipment, and process validation, all in compliance with EU GMP standards.
You’ll work alongside the existing Quality team (including a QP and RP) to ensure all new production areas are fully qualified & validated for medical cannabis manufacturing.
- Ensure all validation activities are aligned with EU GMP and regulatory requirements.
- Conduct risk assessments to determine appropriate validation strategies.
- Support the commissioning and qualification of new production areas.
- Collaborate closely with Quality, Engineering, and Production teams.
- Provide training and guidance to operational teams on validation requirements.
- Help upskill the team.
You must have proven experience in a validation-focused role in Pharmaceuticals / Medical Cannabis / Biotech in a GMP environment with at least 2 years’ experience.
Bonus Points for experience with QA activities and managing a QMS system.
Bonus points for experience with GDP.
Compensation & Benefits:
- ~£35,000–£50,000 base depending on experience (Potential flexibility for Validation superstars)
- ~1-day WFH
- ~ Company pension (All Legal UK Benefits)
- ~ Free on-site parking
- ~ Be part of a pioneering UK company shaping the future of medical cannabis access.
Validation Quality Engineer employer: Lumino
Contact Detail:
Lumino Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Quality Engineer
✨Tip Number 1
Familiarise yourself with the specific EU GMP regulations and guidelines relevant to the pharmaceutical industry, especially those pertaining to medical cannabis. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality.
✨Tip Number 2
Network with professionals in the pharmaceutical and medical cannabis sectors. Attend industry events or join online forums where you can connect with others who have experience in GMP environments. This could lead to valuable insights and potential referrals.
✨Tip Number 3
Prepare to discuss specific validation projects you've worked on in the past. Be ready to explain your role, the challenges you faced, and how you ensured compliance with GMP standards. Real-life examples will make you stand out as a candidate.
✨Tip Number 4
Research the company’s recent developments and their approach to medical cannabis production. Understanding their mission and values will allow you to tailor your conversation during interviews, showing that you're genuinely interested in being part of their pioneering team.
We think you need these skills to ace Validation Quality Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in GMP-regulated environments, particularly in the pharmaceutical or medical cannabis sectors. Emphasise any specific validation projects you've worked on and the skills you've developed.
Craft a Strong Cover Letter: Write a cover letter that directly addresses the job description. Mention your relevant experience, particularly in validation activities and compliance with EU GMP standards. Show enthusiasm for the role and the company's mission in the medical cannabis industry.
Highlight Relevant Experience: In your application, clearly outline your experience with validation processes, risk assessments, and collaboration with quality and engineering teams. Use specific examples to demonstrate your expertise and how it aligns with the company's needs.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a validation role.
How to prepare for a job interview at Lumino
✨Showcase Your GMP Experience
Make sure to highlight your experience in GMP-regulated environments during the interview. Be prepared to discuss specific projects or roles where you ensured compliance with EU GMP standards, as this is crucial for the Validation Quality Engineer position.
✨Understand the Company’s Mission
Familiarise yourself with the company's journey and its role in the medical cannabis industry. Understanding their dual-track approach and recent developments will help you align your answers with their goals and demonstrate your genuine interest in the position.
✨Prepare for Technical Questions
Expect technical questions related to validation processes, risk assessments, and compliance strategies. Brush up on your knowledge of facility, software, equipment, and process validation to confidently answer any queries that may arise.
✨Emphasise Team Collaboration Skills
Since the role involves working closely with Quality, Engineering, and Production teams, be ready to discuss your experience in cross-functional collaboration. Share examples of how you've successfully worked with diverse teams to achieve common goals in previous roles.
