KBI
Manager/Sr Manager, Manufacturing (Purification)
USA - NC - Durham - Hamlin Rd · Senior
Sponsorship not specifiedDetected 19 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.
Responsibilities
- 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:
Requirements
- 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.
Nice to have
- 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.
Benefits
- 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.
Company info
- 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.
Equal opportunity
- KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force.
This listing is sourced directly from KBI's careers page and normalized into a canonical job model.