Manufacturing Technician

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : www.piramalpharmasolutions.com Job Title Manufacturing Technician Job Description Adhere to defined cGMP procedures to manufacture high potency ADC/APIs in support of launched products and clinical trial programmes. Proactive approach to suite readiness, structured monitoring, line clearance, BOM/stock levels, sample control and SAP inventory. Complete GMP documentation accurately Maintain high ESH standards, carrying out all work in accordance with appropriate ESH systems. Adhere to 5s and housekeeping standards so that suites are audit ready at all times. Job Summary** Piramal Healthcare UK Limited is seeking a dedicated Manufacturing Technician to support the production of high-quality pharmaceutical products. This role is crucial for ensuring efficient operation of manufacturing processes and adherence to stringent quality standards within a cGMP environment. Job Responsibilities**

• Operate and monitor manufacturing equipment and machinery according to Standard Operating Procedures (SOPs).
• Perform in-process checks and record data accurately, ensuring compliance with quality control specifications.
• Execute batch record documentation meticulously, including calculations and reconciliation of materials.
• Assist in the setup, changeover, and cleaning of manufacturing equipment and production areas.
• Identify and troubleshoot minor equipment malfunctions, escalating complex issues to appropriate personnel.
• Maintain a clean and organized work environment in accordance with cGMP guidelines.
• Adhere to all health, safety, and environmental regulations and company policies.
• Participate in continuous improvement initiatives to enhance manufacturing efficiency and product quality.
• Collaborate effectively with team members, supervisors, and other departments.

Job Qualifications**

• High School Diploma or equivalent; a technical qualification in a relevant field (e.g., engineering, chemistry, pharmaceuticals) is a plus.
• Previous experience (1-3 years) in a manufacturing or production environment, preferably within the pharmaceutical, biotech, or a highly regulated industry.
• Familiarity with Good Manufacturing Practices (GMP) and Quality Management Systems.
• Ability to read, understand, and accurately follow detailed instructions and SOPs.
• Strong attention to detail and a commitment to producing high-quality work.
• Basic mechanical aptitude and troubleshooting skills.
• Proficient in basic math calculations.
• Good written and verbal communication skills.
• Ability to work effectively in a team-oriented environment.
• Physical ability to stand for extended periods, lift moderate weights, and wear required personal protective equipment (PPE).
• Flexibility to work various shifts, including nights and weekends, as required by production schedules.