Manufacturing Associate I/II – Night Shift

Manufacturing Associate I/II – Night Shift

Requirements

• High school diploma.
• Experience in a regulated industry or demonstrated knowledge of downstream or purification unit operations.
• Ability to follow written instructions.
• Excellent written and verbal communication skills.
• Must be organized and able to focus in a fast-paced, multi-tasked environment and maintain operational efficiency and positive demeanor.
• Energetic, motivated and dynamic individual.
• Must have high attention to detail.
• Ability to work a 12-hour schedule to include weekends, nights and Holidays.

Responsibilities

• Purification of cell culture products per manufacturing batch records in compliance with quality standards, company policies and current regulations. The duties required include, but are not limited to, purification processing using various chromatography, filtration, and viral reduction techniques up through bulk fill of drug product/intermediate.
• Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures.
• Document each task involving manufacturing procedures (i.e. SR’s, EPR’s and BR’s) following GDP at the time of execution.
• Ensure all materials/items are issued and accounted for during the execution of a record (i.e. SR, EPR and BR)
• Demonstrate and apply understanding of current Good Manufacturing Practices (cGMP) and how they apply to specific tasks and responsibilities.
• Participate and be accountable for room 5S.
• Utilize and perform maintenance on equipment per applicable SOP’s.

Preferred Qualifications

• Associates or Bachelor’s degree in a related scientific or engineering discipline
• Biowork certification.
• Experience in single-use platform technology.
• Experience in a CDMO.