API Manufacturing Technician

Job description

Join a multi-disciplinary team supporting the cGMP production of clinical-scale Active Pharmaceutical Ingredients (APIs). In this hands-on manufacturing role, you'll support API development through equipment operation, batch execution, documentation, and continuous improvement activities. Typical process operations include: • Charging solids and liquids to vessels • Distillation, extraction, and phase separation • Crystallization, filtration, and drying • Equipment cleaning and preparation Key Responsibilities • Execute process instructions and batch records in a cGMP environment. • Prepare, operate, monitor, sample, and clean pharmaceutical manufacturing equipment. • Support equipment commissioning, qualification, and troubleshooting activities. • Complete manufacturing documentation, including batch records, cleaning records, and in-process sampling documentation. • Follow cGMP, safety, environmental, and site procedures at all times. • Report deviations, safety concerns, and quality observations promptly. • Manage manufacturing waste according to approved procedures. • Participate in shift handovers and maintain clear communication across teams. • Collaborate with Quality, Compliance, Process Chemistry, Tech Transfer, and Production teams. • Support SOP reviews and continuous improvement initiatives. • Manage priorities independently and assist less-experienced team members as needed. • Complete required training and participate in site safety programs. • Perform routine material handling activities, including lifting and moving items up to 50 lbs. • High School Diploma or GED required. • 4+ years of experience in pharmaceutical, chemical, biotech, or related manufacturing environments. • Experience working in a cGMP-regulated setting. • Working knowledge of production control systems and manufacturing operations. • Strong troubleshooting, problem-solving, and critical-thinking skills. • Highly organized with strong attention to detail and the ability to manage multiple priorities. • Ability to work independently while collaborating effectively within cross-functional teams. • Comfortable working in a manufacturing environment, including standing for extended periods, wearing required PPE, handling hazardous materials, and lifting up to 50 lbs. • Strong written and verbal communication skills. • Proficiency in Microsoft Office applications, including Word and Excel. • Authorization to work in the United States without current or future sponsorship requirements. Preferred Qualifications: • Associate degree (Science or technical discipline) • Strong mechanical aptitude and desire to execute hands on manual labor • Experience with Delta V Production Control System • Experience in a Pharmaceutical cGMP manufacturing environment • Experience performing large scale distillations / Filtrations / milling At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries. PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.