Supervisor, Manufacturing QA (Night Shift)
KBI Biopharma
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Durham, NC
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Mid-Senior level
Posted March 4, 2026
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Responsibilities
Commitments
Responsibilities
- MQA Supervisor routinely collaborates with Manufacturing and work on team initiatives.
- The MQA Supervisor is responsible for coaching and mentoring their teams as needed to foster a GMP compliant site.
- Time Supervise MQA team supporting Manufacturing.
- Provides training, coaching, and mentoring as needed.
- Works directly with MQA team/Manufacturing to resolve deviations and other compliance issues in a timely manner.
- Attend relevant operational meetings as MQA representative
- Perform Change Control assessments for MQA
- Performs client support relating to Batch Record reviews
Commitments
Note: This is a night shift position.
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 authorize KBI Biopharma, Inc. to contact references provided for employment reference checks.
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Requirements
- Bachelor’s Degree or higher degree and appropriate years of experience (at least 6 years) in a Quality or Technical role in a GMP setting required.
- Demonstrated ability to provide leadership to team.
- Strong understanding of technical and compliance regulations for Clinical and Commercial Biopharmaceutical Programs.
- Language Ability: Ability to read and comprehend instructions, correspondence, and memos.
- Ability to write routine correspondence.
- Ability to respond to common inquiries or complaints from employees and/or clients.
- Reasoning Ability: Ability to manage and prioritize multiple efforts independently.
- Ability to write, follow, issue, and explain clear instructions furnished in written and oral form.
- Ability to use risk to make decisions.
- Ability to methodically solve problems to their root causes.
- Math Ability: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.
- Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.
- Physical Demands: Ability to walk job sites, gown into cleanroom areas, lift small equipment and tools.
- Computer Skills: Microsoft Office Programs, E-mail, Electronic Document Management Systems, Electronic Batch Record Systems.
- Equipment Use Computers
Preferred Skills
- 1-2 years of Supervisory experience preferred.
Education
- (Required) – Bachelor’s Degree or higher degree and appropriate years of experience (at least 6 years) in a Quality or Technical role in a GMP setting required.
Note: This is a night shift position.
JOB SUMMARY:
The Manufacturing Quality Assurance (MQA) Supervisor is responsible for supervising the MQA team who supports the Manufacturing Process and Areas as part of a GMP Contract Manufacturing Organization. MQA Supervisors are expected to provide sound guidance to MQA team and Manufacturing with respect to process, SISPQ of product, and risk. The MQA Supervisor’s team shares responsibility for the inspection readiness of the site. MQA Supervisor routinely work on the cleanroom floor directly with the MQA and Manufacturing team to provide real time guidance and support. The Supervisor must adhere to procedures and policies to work on the Manufacturing floor. MQA Supervisor routinely collaborates with Manufacturing and work on team initiatives. The MQA Supervisor is responsible for coaching and mentoring their teams as needed to foster a GMP compliant site.
JOB RESPONSIBILITIES:
Time Supervise MQA team supporting Manufacturing. Provides training, coaching, and mentoring as needed.
Works directly with MQA team/Manufacturing to resolve deviations and other compliance issues in a timely manner.
Attend relevant operational meetings as MQA representative
Perform Change Control assessments for MQA
Performs client support relating to Batch Record reviews
MINIMUM REQUIREMENTS:
Bachelor’s Degree or higher degree and appropriate years of experience (at least 6 years) in a Quality or Technical role in a GMP setting required.
1-2 years of Supervisory experience preferred. Demonstrated ability to provide leadership to team.
Strong understanding of technical and compliance regulations for Clinical and Commercial Biopharmaceutical Programs.
Salary Range: $103,994 - $125,719
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.
Language Ability: Ability to read and comprehend instructions, correspondence, and memos. Ability to write routine correspondence. Ability to respond to common inquiries or complaints from employees and/or clients.
Reasoning Ability: Ability to manage and prioritize multiple efforts independently. Ability to write, follow, issue, and explain clear instructions furnished in written and oral form. Ability to use risk to make decisions. Ability to methodically solve problems to their root causes.
Math Ability: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.
Physical Demands: Ability to walk job sites, gown into cleanroom areas, lift small equipment and tools.
Computer Skills: Microsoft Office Programs, E-mail, Electronic Document Management Systems, Electronic Batch Record Systems.
Equipment Use Computers
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.
JOB SUMMARY:
The Manufacturing Quality Assurance (MQA) Supervisor is responsible for supervising the MQA team who supports the Manufacturing Process and Areas as part of a GMP Contract Manufacturing Organization. MQA Supervisors are expected to provide sound guidance to MQA team and Manufacturing with respect to process, SISPQ of product, and risk. The MQA Supervisor’s team shares responsibility for the inspection readiness of the site. MQA Supervisor routinely work on the cleanroom floor directly with the MQA and Manufacturing team to provide real time guidance and support. The Supervisor must adhere to procedures and policies to work on the Manufacturing floor. MQA Supervisor routinely collaborates with Manufacturing and work on team initiatives. The MQA Supervisor is responsible for coaching and mentoring their teams as needed to foster a GMP compliant site.
JOB RESPONSIBILITIES:
Time Supervise MQA team supporting Manufacturing. Provides training, coaching, and mentoring as needed.
Works directly with MQA team/Manufacturing to resolve deviations and other compliance issues in a timely manner.
Attend relevant operational meetings as MQA representative
Perform Change Control assessments for MQA
Performs client support relating to Batch Record reviews
MINIMUM REQUIREMENTS:
Bachelor’s Degree or higher degree and appropriate years of experience (at least 6 years) in a Quality or Technical role in a GMP setting required.
1-2 years of Supervisory experience preferred. Demonstrated ability to provide leadership to team.
Strong understanding of technical and compliance regulations for Clinical and Commercial Biopharmaceutical Programs.
Salary Range: $103,994 - $125,719
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.
Language Ability: Ability to read and comprehend instructions, correspondence, and memos. Ability to write routine correspondence. Ability to respond to common inquiries or complaints from employees and/or clients.
Reasoning Ability: Ability to manage and prioritize multiple efforts independently. Ability to write, follow, issue, and explain clear instructions furnished in written and oral form. Ability to use risk to make decisions. Ability to methodically solve problems to their root causes.
Math Ability: Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.
Physical Demands: Ability to walk job sites, gown into cleanroom areas, lift small equipment and tools.
Computer Skills: Microsoft Office Programs, E-mail, Electronic Document Management Systems, Electronic Batch Record Systems.
Equipment Use Computers
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.