Pharma 2 Operator

About the role

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs. Cambrex strives to build a culture where colleagues engage in work that matters to customers and patients, learn new skills, enjoy new experiences in an engaging and safe environment, and strengthen connections with coworkers and the community. The company offers a competitive benefits package that includes healthcare, life insurance, retirement planning, and more, and is committed to attracting and nurturing a passionate team of valued professionals in its fast‑paced, growing company. Reporting to the shift supervisor, the Reactor Operator will be expected to successfully produce chemical and pharmaceutical products in the manufacturing environment.

Responsibilities

• Operate batch and continuous type reactors, high pressure reactors, centrifuges, filters, solvent distillation equipment and supporting equipment involved in testing, all according to designated procedures.
• Monitor the equipment; setting controls on valves, vacuums, pumps, pressures, etc., according to designated procedures to achieve desired results.
• Monitors the process variables and makes process control adjustments to maintain the proper process control.
• Use manual and computer-controlled devices to monitor and control the process.
• Clean all equipment used (boil, scrape or scrub out) following designated procedures.
• Assist in training new Pharma Reactor Operators.
• Drum compounds and hazardous waste; label according to set standards; transport to assigned areas.
• Assure area is kept clean and all precautions are taken to prevent environmental spills and control discharge to WWTP at acceptable limits.
• Interpret results and monitor processes using computer-controlled devices.
• Responsible for safe handling of hazardous materials including loading/unloading trucks, processing, packaging and cleanup of equipment.
• Responsible for completion of all operation log books in Pharma area.
• Troubleshoot production line and equipment problems in a safe and effective manner.
• Assist lab personnel with implementing new processes or process changes.
• Complete line entry, confined space, and hot work permits.
• Assist in writing and updating process procedures and SOP’s.
• Adhere to all EPA, FDA and cGMP regulations as they relate to the operation of the chemical production facility.
• Take samples for in-process and Quality Control analysis.
• Perform