Teva Manufacturing Associate II 

United States, Pennsylvania, East Bradford Township 

404877962

ESSENTIAL DUTIES
• Perform routine manufacturing operations related to the preparation of GMP solutions such as handling of raw materials (sampling, weighing, dispensing, formulating), pipetting, titration, filtration and filter integrity testing, and cleaning and disinfection of materials and equipment.
• Set up, operate, and maintain complex manufacturing equipment such as mixers, balances, autoclaves, and parts washers.
• Lead and train junior associates in manufacturing processes and activities.
• Perform all work in a compliant manner in alignment with current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
• Draft, revise, and follow Standard Operating Procedures (SOP’s) and batch records using good documentation practices.
• Identify opportunities for continuous improvement and improved quality compliance.
• Support area management in deviation investigations, change controls, validation protocols, and other activities as needed.
• Collaborate within assigned team and other stakeholders to build a positive and high performing collaborative culture.

MINIMUM REQUIREMENTS
• BS in science or a related field and 3+ years relevant experience in pharmaceutical manufacturing OR 6 + years relevant experience in a pharmaceutical manufacturing environment.
• 1+ years direct experience formulating media and buffer solutions for use in biologics manufacturing.
• Routine use of full face and/or positive air pressure (PAPR) respirators.
PREFERRED REQUIREMENTS
• Experience in upstream, downstream, and/or aseptic fill/finish processing operations
• Experience leading a team or in a supervisory role (formal or informal)
• Experience writing SOP’s, batch records, change controls, and/or deviation investigations.
• Experience or training in Lean Sigma principles and continuous improvement and/or Leadership.

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