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AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Associate Supervisor, Production

North Chicago, Illinois Req ID 2208906 Category Manufacturing & Operations Division AbbVie

Describes the primary goals,objective or function or outputs of this position.


The Associate Supervisor leads a large team to manufacture Pharmaceutical products in a highly compliant
business. Ensures all aspects of the quality system and Safety programs are followed while meeting
production targets to deliver product to customers on time.

Ensures shift targets are established, met, communicated to all relevant stakeholders. Follows up with line
personnel where actuals fall short of target.
Assists Operations Coordinator with staffing lines appropriately based on training qualifications and
development opportunities.
Works closely with Materials Management to align on priorities throughout the shift and respond
accordingly to ensure customer deliveries are met.
Works with shift Training Specialist to ensure compliance while identifying cross training opportunities that
match department needs and personnel development plans.
Ensures cGMP and safety requirements are being met at all times during shift.
Performs required GEMBA walks and STOP for Supervision
Works with fellow supervisor(s) to assess performance of personnel and processes.

Qualifications:
  • Requires a Bachelor's Degree or Equivalent
  • 0-2 years experience in all aspects of manufacturing/Production processes
  • Computer proficiency and and scheduling experience required; good writing skills required
  • Familiarity with industrial automation (e.g. DCS and PLC based system) preferred
  • Working knowledge of safety, quality systems, and cGMP's is required
Significant Work Activities: Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel: No
Job Type: Experienced
Schedule: Full-time
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