AL Solutions
Associate | Sales & Business Development | CDMO/CRO & Biopharma
We are looking for an experienced and hands-on Manufacturing Supervisor to lead daily operations in our drug substance manufacturing facility. In this role, you’ll oversee shift activities and ensure that production meets quality standards, safety requirements, and scheduled timelines. You'll work directly with manufacturing staff, guide day-to-day execution, and contribute to continuous improvement initiatives in a cGMP environment. This is a working supervisor role, meaning you’ll be actively involved on the production floor while also managing personnel and processes Location : Chicago, IL 2nd Shift:
2pm-10pm Responsibilities: Lead and supervise manufacturing activities during assigned shifts. Oversee production of drug substances (upstream and/or downstream), ensuring compliance with batch records and cGMP guidelines. Support and train staff in proper use of equipment, safety procedures, and documentation practices. Review and verify production documentation for completeness and accuracy. Participate in equipment qualifications, validations, and process monitoring. Lead or support investigations and implement corrective and preventive actions (CAPAs). Write and review SOPs and manufacturing records; support process improvements. Collaborate across departments to ensure production schedules and goals are met. Promote safety, compliance, and accountability on the manufacturing floor. Qualifications: Bachelor’s degree in Life Sciences, Engineering, or related field with 5+ years of manufacturing experience Strong hands-on experience in upstream and downstream Familiarity with aseptic processing and cGMP regulations Previous experience leading or supervising manufacturing teams Able to train, motivate, and hold team members accountable Willingness to work assigned shifts and overtime when needed Ability to work in both cleanroom and office environments
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We are looking for an experienced and hands-on Manufacturing Supervisor to lead daily operations in our drug substance manufacturing facility. In this role, you’ll oversee shift activities and ensure that production meets quality standards, safety requirements, and scheduled timelines. You'll work directly with manufacturing staff, guide day-to-day execution, and contribute to continuous improvement initiatives in a cGMP environment. This is a working supervisor role, meaning you’ll be actively involved on the production floor while also managing personnel and processes Location : Chicago, IL 2nd Shift:
2pm-10pm Responsibilities: Lead and supervise manufacturing activities during assigned shifts. Oversee production of drug substances (upstream and/or downstream), ensuring compliance with batch records and cGMP guidelines. Support and train staff in proper use of equipment, safety procedures, and documentation practices. Review and verify production documentation for completeness and accuracy. Participate in equipment qualifications, validations, and process monitoring. Lead or support investigations and implement corrective and preventive actions (CAPAs). Write and review SOPs and manufacturing records; support process improvements. Collaborate across departments to ensure production schedules and goals are met. Promote safety, compliance, and accountability on the manufacturing floor. Qualifications: Bachelor’s degree in Life Sciences, Engineering, or related field with 5+ years of manufacturing experience Strong hands-on experience in upstream and downstream Familiarity with aseptic processing and cGMP regulations Previous experience leading or supervising manufacturing teams Able to train, motivate, and hold team members accountable Willingness to work assigned shifts and overtime when needed Ability to work in both cleanroom and office environments
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