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Manufacturing Supervisor ; 2nd Shift

Job in North Chicago, Lake County, Illinois, 60086, USA
Listing for: BioSpace
Full Time position
Listed on 2026-07-08
Job specializations:
  • Manufacturing / Production
    Regulatory Compliance Specialist, Production Manager
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Supervisor I (2nd Shift-2:30pm-11pm)

About Abb Vie

Abb Vie’s mission is to discover and deliver innovative medicines and solutions 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 including immunology, oncology, neuroscience, and our Allergan Aesthetics portfolio.

Job Description

The Manufacturing Supervisor I works the A2 Shift from 2:30 PM to 11:00 PM, Monday through Friday. The supervisor leads and facilitates safe operations in line with safety, regulatory and operational requirements, ensuring high customer service, product quality, compliance, financial performance and a culture of high performance for the team.

Responsibilities
  • Lead safety initiatives, promote zero safety incidents, conduct safety checks and ensure compliance with all EHS requirements.
  • Manage team deployment, delegate tasks to meet the production schedule, ensure training standards, conduct regular 1:1s, performance reviews and survey action plans.
  • Coordinate shift activities to meet the production schedule and ensure smooth handover to the next manager.
  • Maintain compliance with applicable regulatory agencies, conduct material checks, line clearance checks and spot checks.
  • Manage cycle time and change‑over time, continuously seek and implement improvements.
  • Develop direct reports through training and challenging tasks, maintain development plans and encourage self‑development.
  • Participate in process improvement initiatives to support operational excellence (OpEx).
  • Generate and manage non‑hazardous and hazardous waste in compliance with internal procedures and local and federal regulations.
Qualifications
  • Bachelor’s degree required; degree in sciences or engineering preferred.
  • Pharmaceutical industry experience preferred.
  • Two years of manufacturing or related experience required; supervisory experience preferred.
  • Proficiency in Microsoft Office, SAP and other manufacturing systems.
  • Working knowledge of safety, quality systems and cGMP; strong writing skills.
  • Experience working in an aseptic production environment desirable.
Compensation and Benefits

The base pay range for this position is disclosed based on job grade. Compensation may vary by geographic location. The company offers a comprehensive benefits package, including paid time off (vacation, holidays, sick), medical, dental, vision insurance and eligibility for participation in short‑term incentive programs.

Equal Opportunity Employer

Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.

Reasonable Accommodation

US & Puerto Rico applicants seeking a reasonable accommodation may follow the link provided in the original posting.

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