QC Laboratory Supervisor - 2nd Shift (Pharma)

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); Hybrid; USD 90,000 - 110,000; Full time

Benefits offered by this job

Benefits from day 1

Paid volunteer time

PTO + WTO

Paid holidays

Job summary

Grand River Aseptic Manufacturing (GRAM) seeks a QC Laboratory Supervisor (2nd shift) to lead the Quality Control Lab in Grand Rapids, MI. The role focuses on ensuring accurate testing, safety, and regulatory compliance in a cGMP environment.

Hours are 4:00 pm to 12:30 am, Monday–Friday, with weekend support as needed. You will supervise staff, prioritize work, maintain training records, and drive investigations and CAPAs while upholding safety and quality standards.

Qualifications

• Bachelor’s degree in Chemistry or related discipline with at least 5 years pharmaceutical or testing experience.
• Proficiency in Microsoft Word, Excel, and Outlook.

Responsibilities

• Manage day to day prioritization of routine, in-process, stability, and finished product work.
• Supervises lab personnel, including staff performance and scheduling for coverage.
• Maintain working schedule of all work flowing through the QC Analytical Lab.
• Comply with laboratory safety guidelines; inform management of safety concerns.
• Lead training of all new employees and maintain training records.
• Support OOS system, Laboratory Investigations, CAPAs, and non-conformances.
• Work with management to deliver staff performance evaluations and goal setting.
• Oversee laboratory chemical and equipment use; maintain aseptic technique.
• Independently author or edit internal test methods and SOPs.

Skills

Leadership

Staff scheduling

Laboratory safety

MS Word

MS Excel

MS Outlook

Education

Bachelor’s degree in Chemistry and related discipline

Tools

HPLC

UHPLC

UPLC

GC

UV-Vis

FTIR

Job description

Grand River Aseptic Manufacturing (GRAM) seeks a QC Laboratory Supervisor (2nd shift) to lead the Quality Control Lab in Grand Rapids, MI. The role focuses on ensuring accurate testing, safety, and regulatory compliance in a cGMP environment.

Hours are 4:00 pm to 12:30 am, Monday–Friday, with weekend support as needed. You will supervise staff, prioritize work, maintain training records, and drive investigations and CAPAs while upholding safety and quality standards.