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- Tasks: Join us as a Validation Specialist, ensuring our medical cannabis production meets EU GMP standards.
- Company: Be part of the only Scottish medical cannabis company with EU GMP certifications and domestic cultivation licenses.
- Benefits: Enjoy a competitive salary, hybrid work options, pension, and free on-site parking.
- Why this job: Make a real impact in the medical cannabis industry while working with a top-tier quality team.
- Qualifications: Must have 2+ years of validation experience in GMP-regulated pharmaceutical environments.
- Other info: Opportunity to help shape the future of medical cannabis access in the UK.
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 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 will 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 Quality/ Validation Engineer
✨Tip Number 1
Familiarise yourself with the specific EU GMP standards relevant to medical cannabis production. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to compliance and quality assurance.
✨Tip Number 2
Network with professionals in the pharmaceutical and medical cannabis sectors. Attend industry events or join online forums to connect with others who have experience in GMP environments, as they may provide valuable insights or even 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, as this will showcase your hands-on experience.
✨Tip Number 4
Research the company’s recent developments and their approach to medical cannabis. Being knowledgeable about their operations and future plans will allow you to tailor your conversation during interviews and show genuine interest in their mission.
We think you need these skills to ace Quality/ Validation Engineer
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasise your experience in GMP-regulated environments, particularly within the pharmaceutical or medical cannabis sectors. Use specific examples that demonstrate your expertise in validation activities.
Tailor Your CV: Customise your CV to align with the job description. Focus on your validation skills, any relevant certifications, and your ability to work collaboratively with Quality, Engineering, and Production teams.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your passion for the medical cannabis industry and your understanding of EU GMP standards. Mention how your background makes you a perfect fit for the role.
Showcase Soft Skills: In addition to technical skills, highlight your soft skills such as teamwork, communication, and training abilities. These are crucial for collaborating with various teams and upskilling operational staff.
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 Specialist position.
✨Understand the Company’s Mission
Familiarise yourself with the company's goals and their role in the medical cannabis industry. Demonstrating knowledge about their operations and how they contribute to patient access will show your genuine interest in the position and the company.
✨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 these queries.
✨Emphasise Team Collaboration Skills
Since the role involves working closely with Quality, Engineering, and Production teams, be ready to discuss your experience in collaborative environments. Share examples of how you've successfully worked with cross-functional teams to achieve common goals.
