About Us
Qmed Pharmaceuticals is a growing MHRA-regulated pharmaceutical company specialising in the Over-labelling and distribution of UK licenced medicinal products. Our mission is to deliver safe, high-quality healthcare products while maintaining the highest standards of GMP, GDP, and regulatory compliance.
We recognise that our people are fundamental to our success. We invest in training, development, and continuous improvement, providing employees with opportunities to build their skills and develop rewarding careers within a fast-paced and highly regulated environment.
Job Purpose
The Production Operator is responsible for carrying out batch preparation, over-labelling, packing, re-work, and associated production activities in accordance with approved procedures, Good Manufacturing Practice (GMP), and batch-specific requirements.
The role plays a critical part in ensuring medicinal products are prepared, labelled, packed, and handled accurately while maintaining product quality, patient safety, regulatory compliance, and batch traceability.
Key ResponsibilitiesProduction Activities
· Perform batch preparation activities in accordance with approved SOPs and Work Instructions.
· Select and prepare raw materials, labels, and batch-specific components required for production activities.
· Carry out over-labelling activities in accordance with approved batch documentation and specifications.
· Perform packing, sealing, and labelling activities as instructed.
· Complete approved re-work activities in accordance with authorised procedures.
· Transfer materials and batches between production stages in accordance with approved procedures.
Batch Control & Traceability
· Maintain control and traceability of all batch-specific materials and documentation.
· Ensure materials remain correctly identified, segregated, and secure throughout production activities.
· Ensure only authorised materials are used during production operations.
· Maintain batch integrity and minimise the risk of product mix-ups or contamination.
Documentation & Data Integrity
· Complete Batch Manufacturing Records (BMRs) and associated production documentation accurately and contemporaneously.
· Record production activities clearly, legibly, and in accordance with GMP requirements.
· Follow approved GMP correction practices when completing documentation.
· Ensure all records remain complete, accurate, and traceable.
· Comply with ALCOA+ principles and company data integrity requirements.
Quality & Compliance
· Follow all approved SOPs, Work Instructions, and company procedures.
· Comply with GMP, GDP, Health & Safety, and company quality requirements.
· Identify and report defects, discrepancies, damaged materials, and quality concerns.
· Immediately escalate any issue that may affect product quality, patient safety, compliance, or batch traceability.
· Support investigations by providing factual information when requested.
Health, Safety & Housekeeping
· Follow all Health & Safety policies, procedures, and site rules.
· Wear required personal protective equipment (PPE).
· Maintain clean, organised, and compliant workstations and production areas.
· Report hazards, near misses, accidents, and unsafe conditions promptly.
· Participate in cleaning and housekeeping activities.
Teamwork & Continuous Improvement
· Work collaboratively with Production, QA, Warehouse, and other operational teams.
· Attend and complete required training and competency assessments.
· Support continuous improvement initiatives within the production department.
· Promote a positive, professional, and compliant working environment.
Knowledge, Skills & ExperienceEssential
· Good attention to detail and accuracy.
· Ability to follow written procedures and instructions.
· Good communication and teamwork skills.
· Ability to maintain accurate records and documentation.
· Basic literacy and numeracy skills.
· Ability to work in a structured and regulated environment.
Desirable
· Experience working within a GMP, pharmaceutical, healthcare, food, or regulated manufacturing environment.
· Understanding of Good Manufacturing Practice (GMP) requirements.
· Experience completing production or quality documentation.
Personal Attributes
· High attention to detail.
· Reliable and dependable.
· Quality focused.
· Organised and methodical.
· Able to work effectively as part of a team.
· Committed to maintaining compliance and patient safety standards.
Working Conditions
· Primarily based within GMP-controlled production facilities.
· Regular standing, walking, lifting, and manual handling activities.
· Requirement to wear PPE and comply with hygiene controls.
· May involve handling ambient, cold-chain, and controlled drug products in accordance with approved procedures.
Career Progression
Qmed Pharmaceuticals is committed to developing employees through training and competency programmes. Opportunities may be available to progress into Production Supervisor, Quality Assurance (QA) or other operational and commercial roles based on performance, competency, and business requirements.
Pay: £26,436.80 per year
Benefits:
- Canteen
- Company pension
- Cycle to work scheme
- Free parking
- On-site parking
Work Location: In person
