Quality Assurance Specialist - Pharmaceutical / Medical Cannabis / GMP

JR United Kingdom; Langholm; Hybrid; GBP 30,000 - 60,000; Full time

Job summary

An innovative company in the medical cannabis sector is seeking a Quality Assurance Specialist to enhance GMP operations and manage the Quality Management System. This role is crucial for ensuring compliance with rigorous regulatory standards as the company prepares to launch its own production facility. As part of a small, dynamic team, you will conduct inspections, implement improvements, and train staff, contributing to the pioneering efforts in medical cannabis access in the UK. Join a forward-thinking organization where your expertise will make a significant impact.

Benefits

Company pension

Free on-site parking

1-day work from home

Qualifications

• Proven experience in a Quality Assurance role in Pharmaceuticals.
• Strong knowledge of GMP and hands-on experience with QMS systems.

Responsibilities

• Conduct regular inspections and audits of production processes.
• Implement and monitor GxP systems to ensure compliance.
• Train staff on QA protocols and promote compliance culture.

Skills

GMP

Quality Management Systems (QMS)

Analytical Skills

Collaboration

Attention to Detail

Education

Experience in Pharmaceuticals / Medical Cannabis / Biotech

1-2 years in Quality Assurance

Tools

GxP Systems

SOPs

Job description

Social network you want to login/join with:

Quality Assurance Specialist - Pharmaceutical / Medical Cannabis / GMP, langholm

col-narrow-left

Client:

Lumino

Location:

langholm, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Views:

3

Posted:

05.05.2025

Expiry Date:

19.06.2025

col-wide

Job Description:

Quality Assurance Specialist (GMP)

Medical Cannabis Industry / Pharmaceutical

Location: Dumfries & Galloway, Langholm, Scotland (Hybrid: 4 days on-site, 1 day remote)

Please only apply if you have experience with GMP in a Pharmaceutical company.

Company Overview

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 them 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

Job Summary

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 Quality Assurance Specialist to support GMP operations, manage the QMS system, and help prepare for the final stages of launching their own internal medical cannabis production operations. This will enable the company to offer both UK-produced medical cannabis and internationally sourced products to patients across the country

This is a pivotal role for someone with a strong understanding of GMP principles and Quality Management Systems (QMS), who wants to play an integral role in launching a fully integrated, EU GMP-certified medical cannabis facility.

You will be working closely with the senior QA team to oversee and enhance all QA processes, ensuring the organisation not only maintains its high standards but also meets the rigorous regulatory requirements as they begin production. Experience in validation would be a strong bonus.

Key Responsibilities

• Conduct regular inspections and audits of production processes to ensure compliance with quality standards.
• Implement and monitor GxP systems and identify opportunities for improvement (GMP is essential)
• Analyse quality data and generate reports to track trends and highlight areas of improvement.
• Collaborate with cross-functional teams to implement corrective actions for quality issues.
• Train staff on QA protocols and promote a culture of compliance and continuous improvement.
• Maintain accurate and detailed documentation to ensure traceability and audit readiness.
• Support the validation of systems, equipment, and production rooms in preparation for active manufacturing.
• Assist in the development and refinement of quality procedures and SOPs

Qualifications & Experience

• You must have proven experience in a Quality Assurance role in Pharmaceuticals / Medical Cannabis / Biotech in a GMP environment with at least 1-2 years’ experience.
• You must have a strong knowledge of GMP (Good Manufacturing Practice) and hands-on experience with QMS systems is essential.
• An analytical mindset with strong attention to detail, with a growth mindset
• Effective communicator with excellent collaboration skills.
• Comfortable working in a small startup, where you must be extremely hands on, and roll up your sleeves. We are looking for people who are happy to wear multiple hats.
• Bonus Points for experience with Validation
• Bonus points for experience with GDP
• 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.

How to Apply

If you are interested and would like more information, please apply through this site or email me at [emailprotected]