Sterling Engineering
Pharmaceutical Manufacturing Supervisor
Sterling Engineering, Chicago, Illinois, United States, 60290
Title:
Pharmaceutical Manufacturing SupervisorLocation:
Chicago, ILHire Type:
Direct HireShift:
1st and 3rd shift roles are availableTarget Pay Range:
$40.00 - $50.00/hour + plus overtime pay + bonus
Job Summary:The Manufacturing Supervisor will lead manufacturing operations to produce high-quality, cGMP-compliant pharmaceutical products. Will supervise teams, ensure safety, and meet production goals.
Job Duties:Supervise daily operations and ensure efficient use of resources.Train, develop, and review staff performance.Enforce safety standards and company policies.Oversee SOP training and process compliance.Monitor processes and maintain accurate documentation.Investigate issues, propose solutions, and lead CAPA initiatives.Collaborate cross-functionally to maintain production flow.
Qualifications:Bachelor’s (5+ years’ experience) or Master’s (2+ years’ experience) in Engineering, Pharma, or Life Sciences.Aseptic processing experience preferred.Strong leadership, communication, and problem-solving skills.Proficiency with FDA cGMPs and MS Office.Ability to write technical documents and lead teams.
Pharmaceutical Manufacturing SupervisorLocation:
Chicago, ILHire Type:
Direct HireShift:
1st and 3rd shift roles are availableTarget Pay Range:
$40.00 - $50.00/hour + plus overtime pay + bonus
Job Summary:The Manufacturing Supervisor will lead manufacturing operations to produce high-quality, cGMP-compliant pharmaceutical products. Will supervise teams, ensure safety, and meet production goals.
Job Duties:Supervise daily operations and ensure efficient use of resources.Train, develop, and review staff performance.Enforce safety standards and company policies.Oversee SOP training and process compliance.Monitor processes and maintain accurate documentation.Investigate issues, propose solutions, and lead CAPA initiatives.Collaborate cross-functionally to maintain production flow.
Qualifications:Bachelor’s (5+ years’ experience) or Master’s (2+ years’ experience) in Engineering, Pharma, or Life Sciences.Aseptic processing experience preferred.Strong leadership, communication, and problem-solving skills.Proficiency with FDA cGMPs and MS Office.Ability to write technical documents and lead teams.