Supervisor, Manufacturing Operations (ILP) 2nd Shift

QuVa - Advancing Healthcare Possibilities
Any Location, NJ
Category Operations
Job Description
Supervise ILP operations, label printing activities, and production schedule in accordance with customer demand, prepare reports, and identify continuous improvement opportunities. Develop training programs and conduct training. Work in a safety-sensitive position with a set, consistent schedule.

Requirements

  • High school Diploma or GED from recognized institution or organization
  • 2-3 years prior experience in cGMP / FDA regulated industry
  • 1 year of supervisory or management experience required
  • Successful completion of certified in-house qualification programs
  • Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs.

Benefits

  • Comprehensive health and wellness benefits including medical, dental and vision
  • 401k retirement program with company match
  • 22 paid days off plus 8 paid holidays per year
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