GMP Manufacturing Operator Location: Berlin, Germany Our client is a global powerhouse in the pharmaceutical sector, dedicated to developing and producing high-quality medicines that improve patient health worldwide. With a strong focus on innovation, safety, and operational excellence, the company ensures full compliance with Good Manufacturing Practices (GMP) and all relevant regulatory requirements. Role Summary We are seeking a Manufacturing Operator to join the production team at the Berlin site. This position plays a key role in the reliable and efficient manufacture of pharmaceutical products. You will be directly involved in operating equipment, maintaining strict GMP compliance, and supporting the delivery of safe, effective medicines. Main Responsibilities Operate, monitor, and troubleshoot production equipment in accordance with GMP and company procedures. Carry out equipment cleaning, sterilisation, and set-up for production campaigns. Document all manufacturing activities accurately in line with SOPs and good documentation practice. Execute batch production records (BPR) and maintain related manufacturing documentation. Conduct routine checks and preventative maintenance on equipment. Identify deviations or issues during production and escalate appropriately. Support root-cause investigations and contribute to corrective and preventive actions. Ensure compliance with workplace safety requirements and maintain a clean production environment. Participate in continuous improvement projects and share feedback to optimise efficiency. Assist in onboarding and training of new operators. Skills & Experience Completed vocational training, technical certification, or equivalent qualification in a relevant field. 2–3 years of professional experience in pharmaceutical or biotech manufacturing, ideally in a GMP environment. Hands-on experience with production equipment and cleanroom operations. Strong knowledge of GMP and regulatory compliance in pharmaceutical manufacturing. High attention to detail, accuracy, and responsibility for quality. Team-oriented with strong communication skills. Capable of working independently in a structured, safe, and compliant manner. Flexibility to work in a fast-paced, highly regulated environment. What’s on Offer Competitive remuneration and benefits package. Long-term career prospects with structured development opportunities. A collaborative and international work environment in Berlin. Email applicants; Jake.tookey@discoverinternational.com GMP Drugsubstance Manufacturing Pharmamanufacturing biotechmanufacturing