Manufacturing Team Lead

Piramal Enterprises Ltd. Lexington , KY 40598

Posted 4 weeks ago

Business: Pharma Solution

Department: Operations

Location: Lexington

Job Overview

The Manufacturing Team Lead serves the point person and on-the-floor resource for manufacturing operators, as well as performs all activities related to the preparation, filling, capping, autoclaving, terminal sterilization, compounding, and lyophilization production.

Responsibilities

  • Assists operators by accurately checking processes and tasks or setting-up, trouble-shooting and product change-overs

  • Ensure housekeeping activities are completed, ensure cleanliness and orderliness of manufacturing area at all times

  • Ensure correctness of team's manufacturing documentation

  • Coordinate and provide on-the-job training to new hires

  • Perform end-of-shift reports, as needed

  • Performs line clearances, cleaning/sanitization, cleaning, preparing and sterilization of fill equipment, sterilization of components, operation of aseptic filling equipment, filter testing, operation vial washing equipment

  • Operate and maintain production related equipment

  • Weigh, measure and check raw materials to assure batches manufactured contain proper ingredients and quantities

  • Execute validation protocols for processes and equipment

  • Maintain records and a clean environment to comply with regulatory requirements

  • Read, understand, and comply with Good Manufacturing Practices and Standard Operating Procedures.

  • Assists operators by accurately checking processes and tasks or setting-up, trouble-shooting and product change-overs

  • Monitor and may perform daily operations and provide direction to staff as needed to maintain safe and cGMP compliant work environment.

  • Monitor batch production records and documentation entries throughout the manufacturing/packaging/inspection process to ensure timely closure.

  • Helps to ensure compliance with all government and company regulatory requirements to ensure applications of cGMP compliance with respect to staff, areas, documentation, and quality requirements.

  • Other duties as assigned

Education

  • High School education or equivalent

Experience

  • Minimum 2 years of experience in an aseptic, or other cGMP pharmaceutical manufacturing environment

Competencies

  • Ability to communicate effectively and lead a team

  • Mechanical aptitude, ability to operate processing equipment

  • Prior knowledge and/or ability to understand and follow job related regulatory requirements (cGMP, OSHA, FDA)

  • Ability to read, interpret, and follow written instructions

  • Team player committed to quality and working effectively with others

  • Track record of consistent attendance and overall reliability

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