Night-Shift Biopharma Manufacturing Supervisor

KBI Biopharma

North Carolina

On-site

USD 85,000 - 110,000

Full time

14 days+

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Job summary

KBI Biopharma in North Carolina is seeking a Solution Prep Manufacturing Supervisor for the 12-hour night shift (2-2-3). You will lead a team responsible for upstream and downstream preparation of solutions and growth media used to process biopharmaceutical products, ensuring Right First Time execution and strict compliance with cGMP.

Responsibilities include coaching staff, authoring SOPs, CAPAs, and coordinating with MS&T, PD, QA, and Facilities.

Qualifications

Bachelor’s degree in a related scientific or engineering field with 4+ years of cGMP manufacturing experience or equivalent.
Preferred knowledge of mammalian cell culture or microbial fermentation for biopharmaceutical production.
Experience with single-use platform technology is preferred.
Knowledge of quality systems and regulatory expectations is preferred.
Excellent written and verbal communication skills in English.
Organized and able to maintain efficiency in a fast-paced environment.
Fluency in reading/writing English; ability to read safety and operation manuals and write routine reports.

Responsibilities

Support daily production tasks to maintain schedule adherence in a cGMP environment.
Supervise, coach, mentor, and train team members for compliant execution.
Ensure equipment and facilities are maintained and work orders are completed.
Author, train, and review manufacturing procedures.
Drive process improvements; troubleshoot issues; track metrics; manage deviations and CAPAs.