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- Tasks: Plan and execute validation activities for a new medical cannabis production facility.
- Company: Join the only Scottish medical cannabis pharmaceutical company with EU GMP certifications.
- Benefits: Enjoy a competitive salary, hybrid work options, and a company pension.
- Why this job: Be part of a pioneering team shaping the future of medical cannabis access in the UK.
- Qualifications: Must have 2+ years of experience in a GMP-regulated pharmaceutical environment.
- 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, with 12 employees, 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. For the past two years, they’ve been importing EU GMP medical cannabis medicines from global partners and supplying to the UK market for patients. 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.
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 medical cannabis industry. This knowledge will not only help you understand the role better but also demonstrate your commitment and expertise during discussions.
✨Tip Number 2
Network with professionals in the pharmaceutical and medical cannabis sectors. Attend industry events or join relevant online forums to connect with others who can provide insights or even referrals to the company.
✨Tip Number 3
Prepare to discuss your previous validation experiences in detail, particularly any challenges you faced and how you overcame them. This will showcase your problem-solving skills and practical knowledge in a GMP environment.
✨Tip Number 4
Research the company’s recent developments and their approach to medical cannabis production. Being well-informed about their operations and goals will allow you to tailor your conversation and show genuine interest in contributing to their mission.
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 environments, particularly within the pharmaceutical or medical cannabis sectors. Use specific examples of validation activities you've been involved in to demonstrate your expertise.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for the medical cannabis industry. Mention how your skills align with the company's mission and the specific role of Validation Specialist.
Highlight Relevant Experience: In your application, emphasise any previous roles where you conducted validation activities, risk assessments, or collaborated with cross-functional teams. This will show that you have the necessary background for the position.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a GMP-regulated environment.
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 challenges you've faced and how you overcame them, as this will demonstrate your expertise and suitability for the role.
✨Understand the Company’s Mission
Familiarise yourself with the company's goals and values, especially their focus on medical cannabis. Showing that you understand their mission and are passionate about contributing to it can set you apart from other candidates.
✨Prepare for Technical Questions
Expect technical questions related to validation processes, risk assessments, and EU GMP standards. Brush up on these topics and be ready to explain your thought process and methodologies clearly.
✨Demonstrate Team Collaboration Skills
Since the role involves working closely with various teams, be prepared to discuss your experience in collaborative environments. Share examples of how you've successfully worked with Quality, Engineering, and Production teams in the past.
