• Job Description

  Req#: R00007268

  Job Summary

  The Manager/Sr. Manager, Manufacturing Specialists is responsible for providing technical leadership and oversight of the quality systems for the Manufacturing department. The Manager leads a team of compliance and technical specialists, possesses proven technical writing and problem-solving skills, and has a drive for continuous improvement. The Manager has experience using single-use disposable technologies and an understanding of upstream processing, downstream processing, and general biomanufacturing support principles.

  From a technical perspective, the Manager leads a team responsible for system ownership activities such as generating manufacturing procedures and records, supporting procurement and enrolling of manufacturing equipment, driving operational excellence initiatives and other activities required of responsible system owners. Team members also serve as a point of contact for equipment issues and inventory management issues.

  From a compliance perspective, the Manager leads a team that supports thorough and robust manufacturing investigations, implement effective corrective/preventative actions, lead manufacturing compliance and safety walkthroughs, oversee internal and external audits, and manage manufacturing change controls. Additionally, the Manager is responsible for performance metrics and oversight for all manufacturing systems. The Manager is responsible for ensuring their staff works cross-functionally with QA, MS&T, Engineering, Supply Chain, IT, AFS and other key departments to ensure manufacturing operations are successful, reliable, and compliant. This requires a drive for continuous improvement, simplicity and superior equipment and human performance.

  Job Responsibilities

  • Manage, train and mentor a team of Manufacturing Specialists that implement thorough and effective corrective and preventative actions, drive training initiatives around compliance and support post-execution review of manufacturing records/data. Oversee the team as they take responsibility for performing area walkthroughs and manage inspection readiness and audit responses and actions.

  • Manage, train and mentor a team of Manufacturing Specialists that generates manufacturing procedures and records, drives operational excellence initiatives, supports procurement and enrollment of manufacturing equipment, support comprehensive investigations to determine root cause/product impact, and performs other activities as responsible system owners.

  • Drive process improvement initiatives, troubleshoot issues, track and trend metrics, and author/review/approve technical documents, procedures, CAPAs, and change controls.

  • Supervise, coach, mentor, and train team members to maintain educated, qualified, and motivated employees. Ensure staff maintain a high level of compliance to procedures and quality expectations.

  Minimum Requirements

  Manager: Bachelor’s degree in a related scientific or engineering discipline is preferred and 8+ years’ experience in related GMP manufacturing operations; 3+ years prior leadership/supervisory experience

  Sr. Manager: Bachelor’s degree in a related scientific or engineering discipline is preferred and 10+ years’ experience in related GMP manufacturing operations; 5+ years prior leadership/supervisory experience (preferred).

  Demonstrated knowledge of cell culture, fermentation, or purification unit operation is preferred. Experience in single-use platform technology is preferred. Excellent written and verbal communication skills are required. Energetic, motivated and dynamic individual. Must be organized and able to focus in a face-paced, multi-tasked environment and maintain operational efficiency and positive demeanor.

  Salary Range: Manager: $118,000 - $162,800 ; Senior Manager ; $133,000 - $183,700

  Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate’s qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.

  About KBI:

  KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit www.kbibiopharma.com .

  KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds – regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status – and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.

  KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.

  KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. 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. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

  I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

• About the company

  KBI Biopharma Inc. is a global Contract development and manufacturing organization (CDMO / CMO) offering Cell Line Development, Process Analytical & Formulation Development, Clinical & Commercial Manufacturing, Characterization & Cell Therapy services,...

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