Manufacturing Supervisor I (2nd Shift-2:30pm-11pm)
AbbVie
August 20, 2026
On-site
North Chicago, IL
$75,000 - $142,500 USD yearly
Operations
This is for the A2 Shift 2:30PM–11pm, Monday–Friday.
Role Overview:
The Manufacturing Supervisor I has basic knowledge and experience in its field and develops competence by performing structured work. Lead and facilitate safe operations in line with all safety, regulatory and operational requirements; assure delivery of high customer service, ensure product/service quality, comply with regulatory requirements, achieve financial performance (including cost reductions), and build a culture of high performance.
Responsibilities:
- Safety: Drive safety improvements; conduct routine safety checks; promote zero safety incidents in compliance with all EHS requirements.
- People: Deploy team members daily to meet production schedule; delegate tasks; ensure required training; conduct 1:1s, performance reviews, and survey action plans; ensure weekly time & attendance approval; cascade important information.
- Operational: Coordinate shift activities to meet production schedule; ensure smooth shift handover.
- Compliance: Ensure compliance with regulatory agencies; perform material/line clearance/spot checks; manage compliance issues impacting lot completion.
- Performance: Manage cycle time and change-over time; identify improvements.
- Development: Secure training, assign progressively challenging tasks; maintain development plans; demonstrate a growth mindset.
- OpEx: Participate in process improvement initiatives.
- Waste Management: Generate and manage non-hazardous/hazardous waste per internal procedures and local/federal regulations.
Qualifications:
- Bachelor’s degree required; sciences or engineering strongly preferred.
- Pharmaceutical industry experience strongly preferred.
- Two years manufacturing or related experience required; supervisor experience preferred.
- Proficient in Microsoft Office and manufacturing systems (e.g., SAP).
- Working knowledge of safety/quality systems and cGMPs required; familiarity with regulated documentation; good writing skills.
- Aseptic production environment experience desirable (if applicable).
Role Overview:
The Manufacturing Supervisor I has basic knowledge and experience in its field and develops competence by performing structured work. Lead and facilitate safe operations in line with all safety, regulatory and operational requirements; assure delivery of high customer service, ensure product/service quality, comply with regulatory requirements, achieve financial performance (including cost reductions), and build a culture of high performance.
Responsibilities:
- Safety: Drive safety improvements; conduct routine safety checks; promote zero safety incidents in compliance with all EHS requirements.
- People: Deploy team members daily to meet production schedule; delegate tasks; ensure required training; conduct 1:1s, performance reviews, and survey action plans; ensure weekly time & attendance approval; cascade important information.
- Operational: Coordinate shift activities to meet production schedule; ensure smooth shift handover.
- Compliance: Ensure compliance with regulatory agencies; perform material/line clearance/spot checks; manage compliance issues impacting lot completion.
- Performance: Manage cycle time and change-over time; identify improvements.
- Development: Secure training, assign progressively challenging tasks; maintain development plans; demonstrate a growth mindset.
- OpEx: Participate in process improvement initiatives.
- Waste Management: Generate and manage non-hazardous/hazardous waste per internal procedures and local/federal regulations.
Qualifications:
- Bachelor’s degree required; sciences or engineering strongly preferred.
- Pharmaceutical industry experience strongly preferred.
- Two years manufacturing or related experience required; supervisor experience preferred.
- Proficient in Microsoft Office and manufacturing systems (e.g., SAP).
- Working knowledge of safety/quality systems and cGMPs required; familiarity with regulated documentation; good writing skills.
- Aseptic production environment experience desirable (if applicable).