Manufacturing Operations Supervisor

1 week ago


Durham, North Carolina, United States KBI Biopharma Full time

Job Overview

The Manufacturing Operations Supervisor plays a crucial role in guiding a team of production associates engaged in the upstream or downstream processing of bulk intermediates and/or bulk drug substances within the biopharmaceutical sector. This position entails planning, delegating, and overseeing daily operations to ensure timely execution while adhering to safety and quality standards, including current Good Manufacturing Practice (cGMP).

In addition to managing daily responsibilities, the Supervisor will spearhead project teams, develop standard operating procedures (SOPs) and Master Batch Records (MBRs), implement corrective and preventive actions (CAPAs), and contribute to the qualification of facilities and equipment.

A successful Supervisor will leverage their knowledge of upstream and downstream processing equipment to mentor colleagues, troubleshoot issues, and optimize daily workflows. The role also includes overseeing personnel tasked with maintaining the cleanliness of GMP facilities.

Key Responsibilities:

  • Plan and schedule daily production activities.
  • Facilitate manufacturing processes while ensuring compliance with established procedures.
  • Supervise and mentor team members to enhance their skills and performance.
  • Oversee the maintenance and operation of equipment and facilities.
  • Drive initiatives for process improvement and operational efficiency.

Qualifications:

Candidates should possess a Bachelor's degree in a relevant field along with several years of experience in cGMP manufacturing environments. Leadership or supervisory experience is highly desirable. Strong communication abilities, organizational skills, and proficiency in English, both written and verbal, are essential for success in this role.



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