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Manufacturing Maintenance Supervisor - 3rd Shift Full-time

at TRIS PHARMA INC in New Jersey (Published at 08-03-2019)

Tris Pharma, Inc. (www.trispharma.com) is a rapidly growing, technology-driven pharmaceutical company engaged in branded and generic product development. Located in Monmouth Junction, New Jersey, Tris has an immediate opening for a Manufacturing Supervisor ? 3rdt shift.

The Manufacturing Supervisor oversees all aspects of manufacturing methods and processes for new or existing products, implements and maintains production schedules and manpower requirements to meet scheduling needs. This is a 3rd Shift Position.

Responsibilities include but not limited to:

  • Accomplishes manufacturing staff results by communicating job expectations; planning, monitoring, and appraising job results; coaching and counseling employees; initiating, coordinating, and enforcing systems, policies, and procedures; Provides guidance, support and direction through positive interactions with manufacturing associates during daily operations
  • Organizes the daily schedule and assigns personnel to the various work spaces to meet the demand of planning
  • Works collectively with the other Supervisors to assist in setting up the daily schedule and providing coverage for absenteeism
  • Assures that all Drug Enforcement Agency (DEA) requirements are being followed with respect to the production of controlled substances
  • Reports and investigates any deviations from processes or procedures
  • Maintains a presence on the production floor at all times; Trains new employees and mentors lower level technicians as appropriate
  • Assists with the development and writing of SOPs and investigation reports and contributes to the circulation of the documents under approved procedures
  • Possesses total comprehension and working knowledge of the manufacturing equipment and manufacturing processes in designated areas
  • Maintains safe and clean work environment by educating and directing personnel on the use of all control points, equipment, and resources; maintaining compliance with established policies and procedures
  • Issues work orders, as required
  • Works extra hours or weekends as required by management to meet the demands of the schedule

Qualifications:

High School diploma or equivalent AND minimum 10 years related work experience OR Associates degree AND 7 years related work experience OR Bachelors degree AND minimum 5 years related work experience . Related work experience must include multiple aspects of the manufacturing process in a pharmaceutical or biotechnology cGMP regulated environment.

  • Working knowledge of manufacturing procedures and federal regulations pertaining to manufacturing processes
  • Working knowledge of good manufacturing systems and familiarity with regulatory and manufacturing SOPs and cGMPs
  • Demonstrated ability to read and interpret documents such as safety and environmental policies, operating and maintenance instructions and procedure manuals, etc.
  • Strong record keeping skills
  • Prior pharmaceutical manufacturing group lead or supervisory experience
  • Ability to train, motivate, direct and supervise manufacturing personnel
  • Proficiency with Microsoft Office

Tris Pharma, Inc. offers a highly competitive compensation and benefits package. Tris Pharma, Inc. is an Equal Opportunity Employer.



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