• AbbVie
  • $99,000.00 -130,420.00/year*
  • Calumet City, IL
  • Manufacturing
  • Full-Time
  • 736 Campbell Ave

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About AbbVie

is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the worlds most complex and critical conditions. The companys mission is to use its expertise, dedicated people and unique approach to innovation to markedly improve treatments across four primary therapeutic areas: immunology, oncology, virology and neuroscience. In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world. For more information about AbbVie, please visit us at

AbbVie: Determined to Make a Difference [Updated]

People. Passion. Possibilities. Those three simple words mean everything at AbbVie, where patients always come first. So do cutting-edge science and innovation, which fuel our expanding pipeline as we take on the world's toughest health challenges in oncology, immunology, liver disease, women's health and beyond. Together, we strive to make a difference for patients around the world. For more visit: www.abbvie.com.

Responsible for the daily supervision and training of operating personnel in the production of clinical or commercial products. Works in concert with other supervisors. Responsible for the accurate and timely completion of production related cGMP documentation. Responsible for implementation of manufacturing procedures. Ensures the effective use of material, equipment, and personnel in producing quality products. Key Responsibilities Include: Key Responsibilities Include: Reviews daily production schedule and priorities to determine unit (suite) assignments and critical actions. Reviews all materials and batch records required to support shift and any off-shift needs for the day. Provides on the floor training to support formalized technical and cGMP training. Checks that operator training files match and support the processes they are required to carry out. Monitors operator training files and works with compliance specialist to keep files up to date. Works with QA and Subject Matter Expert (Tech Ops or Process Sciences) to resolve exceptions. Works with technology transfer team to incorporate new processes in the plant. Reviews new Batch records and SOPs. Provides supervision primarily to skilled nonexempt and junior level exempt employees. Acts as advisor to unit or sub-unit, becomes actively involved as required. Acts as mentor for less senior personnel. Evaluates staff performance. Basic: Requires a Bachelors degree or equivalent. Five plus years experience in all aspects of manufacturing/ production processes Computer proficiency and scheduling experience required; good writing skills required. Familiarity with industrial automation (e.g., distributed control and PLC-based systems) Working knowledge of safety, quality systems, and cGMPs is required Equal Opportunity Employer Minorities/Women/Veterans/Disabled

Additional Information

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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