KBI Biopharma

Manager/Sr Manager, Manufacturing (Purification)

USA - NC - Durham - Hamlin Rd · Senior

Sponsorship not specifiedDetected 20 days ago

Process ImprovementGMPCell CultureLeadershipCommunicationMentoring

About the role

The individual will ensure that manufacturing records and materials are available for timely execution of activities to meet production schedules.
The ideal candidate will be both technically sound as well as an experienced team motivator and coach.

Strategic lead on high-profile projects
Inter Departmental coordination and scheduling support.
Support operations to ensure MRP transactions, manufacturing record reviews, and maintenance activities are completed timely and thoroughly.
Support operations to ensure deviations, CAPAs, and Change Controls are completed timely and thoroughly.
Identify and implement continuous improvement projects to increase safety, reliability, speed, and quality.
Direct support to Director, Manufacturing on daily tasks.
Manufacturing Operations Support:

Excellent written and verbal communication skills with application in a team-oriented environment are required.
Must be organized and able to focus in a face-paced, multi-tasked environment and maintain operational efficiency and positive demeanor
This proven and qualified candidate will use their past experiences, depth and knowledge of biopharmaceutical operations to teach, troubleshoot, and continuously improve the production operations at the facility.
Demonstrated knowledge of mammalian cell culture, purification, and solution preparation activities is expected as the Manager/Sr.

Bachelor's degree in a related scientific or engineering discipline is preferred and 8+ years' experience in related GMP manufacturing operations
3+ years prior supervisory experience.
Bachelor's degree in a related scientific or engineering discipline is preferred and 10+ years' experience in related GMP manufacturing operations
5+ years prior supervisory experience preferred.
Working conditions associated with this position include working 8-hour shifts M-F.
The job requires working within a cGMP manufacturing biotechnology facility which requires clean room operations.
Clean room operations require donning clean room attire when entering clean room areas and maintaining good personal hygiene.
While performing the duties of this job the employee oversees staff who utilize equipment and materials which include mechanical hazards, chemical hazards, electricity hazards, and tripping and falling hazards.

Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force.

This listing is sourced directly from KBI Biopharma's careers page and normalized into a canonical job model.