Manufacturing Supervisor I (2nd Shift-2:30pm-11pm)

BioSpace; North Chicago (IL); On-site; USD 68,000 - 92,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Performance incentives

Job summary

AbbVie is hiring a Manufacturing Supervisor I to lead safe, compliant production operations on multiple shifts. You will drive team performance, ensure quality and regulatory compliance, and manage resources to meet the production schedule.

The role emphasizes developing staff through training, conducting performance reviews, and implementing process improvements within a regulated environment. A strong emphasis on safety and operational excellence is required.

Qualifications

• Bachelor's degree required; sciences/engineering preferred.
• Pharmaceutical industry experience strongly preferred.
• Two years of manufacturing or related experience required; supervisor experience preferred.
• Proficient in Microsoft Office and other manufacturing systems, such as SAP.
• Working knowledge of safety, quality systems, and cGMPs; strong writing skills.
• Aseptic production experience desirable.

Responsibilities

• Lead safe operations and ensure compliance with safety, regulatory, and operational requirements.
• Deploy and develop team members; conduct 1:1s and performance reviews; manage attendance and communicate information effectively.
• Coordinate shift activities to meet production schedule and ensure smooth handovers.
• Maintain compliance with regulatory agencies; perform material checks, line clearance, and spot checks.
• Manage cycle time and change-over improvements; drive OpEx initiatives.
• Develop direct reports with training and growth opportunities; foster growth mindset.
• Participate in process improvement initiatives.
• Generate and manage waste per internal procedures and regulations.

Skills

Safety leadership

Team coordination

Regulatory awareness

Education

Bachelor's degree in science or engineering

Tools

SAP

Microsoft Office

Job description

About AbbVie

AbbVie'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 and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Company Description

About AbbVie

AbbVie'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 and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Job Description

The role of the Manufacturing Supervisor I has basic knowledge and experience in its field and develops competence by performing structured work. Receives guidance and direction from more senior peers. Lead and facilitate safe operations in line with all safety, regulatory and operational requirements. Assure the delivery of high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build a culture of high performance for the team.

Available Shifts

1st Shift- 6:30am-3:00pm
2nd Shift- 2:30pm-11:00pm
3rd Shift- 10:30pm-7:00am

Responsibilities

• Safety: Create an environment where safety is the number one priority in every activity that you do, driving safety improvements and conducting safety checks routinely. Be present on the floor promoting a culture of zero safety incidents in compliance with all EHS requirements.
• People: Responsible for daily effective deployment of team members and ensure tasks are appropriately delegated to meet the production schedule. Ensure that team members are trained to the required standards of their job. Drives engagement with team by having regular 1:1s, conducts performance reviews and has survey actions plans in place. Ensure time and attendance is approved on time each week so that employees are paid correctly. Communicating effectively with team cascading important info.
• Operational: Responsible for the effective coordination of the activities within the shift to meet the production schedule. Ensure a smooth shift handover with the next manager to ensure departmental activities are planned and executed safely.
• Compliance: Ensure compliance with applicable regulatory agencies. Execute a proactive compliance management process where material checks, line clearance checks and spot checks are conducted routinely. Effectively manage any compliance issue that arises during shift that could potentially impact on lot completion.
• Performance: Responsible for complete cycle time management and continuously seek to identify improvements. Responsible for change-over time management and continuously seek to identify improvements.
• Development: Develop direct reports by securing appropriate training and assigning progressively challenging tasks. Ensures all personnel has development actions/ plans in place and arranging opportunities for growth. Be proactive in self-development by having a growth mindset towards personal development.
• Operation Excellence (OpEx): Participates in process improvement initiatives.
• Generates and manages non-hazardous and hazardous waste, according with the internal operating procedures and in compliance with local and federal regulations.
  

Qualifications

• Bachelors degree is required. A degree in sciences or engineering is strongly preferred.
• Pharmaceutical Industry experience is strongly preferred.
• Two years of manufacturing or related experience required. Supervisor experience preferred.
• Experience Systems: Proficient in Microsoft Office and other manufacturing systems, such as SAP.
• Experience Regulatory: Working knowledge of safety, quality systems, and cGMPs is required. Familiarity with documentation in a highly regulated environment; good writing skills.
• Experience Aseptic (If applicable): Experience working in an aseptic production environment desirable.
  

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this roleat thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on manyfactors including geographiclocation,andwemay ultimately pay more or less than the posted range. This range may bemodified in thefuture.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
• This job is eligible toparticipate in our short-term incentiveprograms.
  

Note: No amount of payis considered to bewages or compensation until such amount isearned, vested, anddeterminate.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat areallocable to a particular employeeremains in the Company'ssoleandabsolutediscretion unless and until paid andmay bemodified at the Companys sole and absolutediscretion, consistent withapplicable law.

AbbVie 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.

US & Puerto Rico only - to learn more, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html