Evening QC Lab Supervisor – cGMP Pharma, 2nd Shift

Grand River Aseptic Manufacturing, Inc.; Grand Rapids (MI); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Benefits starting day 1

Paid volunteerism starting day 1

Paid time off (PTO) + Wellness TimeOff

10 paid holidays per year

Job summary

Grand River Aseptic Manufacturing, Inc. (GRAM) seeks a QC Laboratory Supervisor for the 2nd shift to lead the QA/QC lab team in a cGMP environment. The role focuses on prioritizing testing work, ensuring safety, and maintaining documentation and training.

Hours are 4:00 pm to 12:30 am, Monday–Friday, with weekend support as production schedules require. Strong background in chemistry and pharmaceutical testing is essential.

Qualifications

• Bachelor’s degree in Chemistry or related discipline; minimum 5 years pharma/testing experience.
• Proficient computer skills in Microsoft Word, Excel, and Outlook.
• Knowledge of cGMP drug manufacturing environments is preferred.

Responsibilities

• Manage day-to-day prioritization of routine, in-process, stability, and finished product work.
• Supervises lab personnel, schedules overtime/weekend coverage for manufacturing support.
• Maintain working schedule for all work flowing through the QC Analytical Lab.
• Comply with laboratory safety guidelines; inform management of safety concerns.
• Lead training of new employees and maintain training documentation.
• Support OOS system, lab investigations, and assist CAPAs/non-conformances.
• Deliver staff performance evaluations and set individual goals.
• Oversee laboratory chemical handling and equipment use.
• Establish aseptic technique and edit internal methods/SOPs.

Skills

Laboratory supervision

Regulatory knowledge (FDA/ICH/EMA)

Analytical mindset

Education

Bachelor's degree in Chemistry or related

Tools

HPLC

UHPLC

UPLC

GC

UV-Vis

FTIR

Job description

Grand River Aseptic Manufacturing, Inc. (GRAM) seeks a QC Laboratory Supervisor for the 2nd shift to lead the QA/QC lab team in a cGMP environment. The role focuses on prioritizing testing work, ensuring safety, and maintaining documentation and training.

Hours are 4:00 pm to 12:30 am, Monday–Friday, with weekend support as production schedules require. Strong background in chemistry and pharmaceutical testing is essential.