Production Operative

My client based in Beeston is currently recruiting for multiple production operatives to work across various different sectors within the manufacturing plant. This role requires people who are flexible and able to work days, afternoons and nights you will receive notice of a shift change within 2 weeks, it is imperative that you are able to work ALL shifts. Weekly pay ongoing work. Role Overview As a Production Operative in a pharmaceutical manufacturing environment, you will be responsible for operating production equipment, monitoring processes, and ensuring the consistent manufacture of products in accordance with Good Manufacturing Practice (GMP) standards. This role requires precision, attention to detail, and a strong commitment to quality, safety, and continuous improvement. Key Responsibilities Manufacturing Operations Operate, monitor, and maintain pharmaceutical production machinery according to Standard Operating Procedures (SOPs). Perform equipment setup, changeovers, and cleaning following validated procedures. Weigh, measure, and dispense raw materials and components accurately as per batch documentation. Conduct in-process checks (e.g., weight, fill volume, visual inspection) and record data accurately. Quality and Compliance Maintain cleanliness and organisation of the work area in line with Good Housekeeping. Complete batch records, cleaning logs, and material traceability forms accurately and in real time. Support audits and assist in the implementation of corrective and preventive actions (CAPAs). Handle materials and products according to contamination control, product segregation, and hygiene standards. Health, Safety & Environment (HSE) Follow all Health, Safety, and Environmental policies and site procedures. Use personal protective equipment (PPE) correctly and report any unsafe conditions immediately. Support a zero-incident culture through hazard identification, near-miss reporting, and safe working practices. Manage waste and recycling in compliance with environmental and sustainability policies. Continuous Improvement & Teamwork Collaborate with Engineering, Quality, and Supply Chain teams to resolve issues efficiently. Suggest and implement improvements to product quality, process efficiency, and workplace safety. Support the training and development of new or less experienced team members. Skills, Experience & Qualifications Essential High attention to detail and accuracy in completing documentation. Ability to follow written and verbal instructions precisely. Strong communication and teamwork skills. Basic IT literacy (e.g., experience using production or quality systems such as SAP or MES). Good numeracy and literacy skills. Personal Attributes Reliable, punctual, and safety-conscious. Proactive and able to identify and solve problems effectively. Adaptable and able to work in a fast-paced, regulated environment. Flexible to work rotating shifts, weekends, or overtime as required. Takes pride in producing high-quality products and maintaining compliance. Working Conditions Cleanroom or controlled pharmaceutical manufacturing environment. Shift-based work (e.g., rotating day/night shifts). Physically active role involving standing for long periods and manual handling of up to 25kg. Strict hygiene and gowning requirements. Benefits Competitive salary and shift allowance. Training and career development opportunities. Supportive team environment with strong focus on safety and quality. Contribution to manufacturing products that improve health and wellbeing globally. IF THIS ROLE IS OF INTEREST PLEASE CALL RUBIE ON (phone number removed) OR APPLY ONLINE NOW #J-18808-Ljbffr