Experience

Bioserv Corporation

• United States
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Manufacturing Associate 1

  • Sep 2022 - Present

  GENERAL PURPOSE OF JOB: The Manufacturing Associate I is responsible for performing semi-routine procedures and analysis, associated with the manufacturing process. Champion safety, process improvement and compliance. This role is responsible for the manufacture of products in compliance with current Good Manufacturing Practice (GMP), regulatory entities, supporting the implementation of new equipment processes, and industry best practices in support of the organization's goals and objectives. ESSENTIAL DUTIES AND RESPONSIBILITIES: Participate in cGMP manufacturing processes. Maintain GMP-controlled environments in clean rooms and equipment. Stage materials and equipment prior to manufacturing activities. Responsible for supporting essential supply inventory and equipment. Review and revise current Good Manufacturing Practice (cGMP), Batch Production Records, SOPs, protocols, and reports. Perform daily monitoring of equipment and assist Facilities and Engineering personnel as necessary on equipment maintenance and calibration. Adhere to good documentation practices that meet GMP guidelines. Provide support to cross-functional teams to meet production or timeline demands. Perform environmental monitoring, identify discrepancies, and complete associated documents. Perform aseptic filtration, filling and crimping of product. Support the introduction of new manufacturing equipment. Performs other duties as assigned. Show less



Genalyte, Inc.

• United States
• Biotechnology
• 1 - 100 Employee

• Manufacturing Technician

  • Oct 2019 - Sep 2022



GenMark Diagnostics

• United States
• Medical Equipment Manufacturing
• 300 - 400 Employee

• Manufacturing Technician

  • Nov 2017 - Oct 2019