What are the responsibilities and job description for the Manager / Sr. Manager, Manufacturing Specialists position at KBI Biopharma?
At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.
Position 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. 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. The Manager is responsible for ensuring their staff works crossfunctionally 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.
Responsibilities:
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:
XXXXXXXXXX For Manager
XXXXXXXXXX For Senior Manager
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, 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.
Position 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. 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. The Manager is responsible for ensuring their staff works crossfunctionally 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.
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.
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:
XXXXXXXXXX For Manager
XXXXXXXXXX For Senior Manager
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, 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.