Miltenyi Biotec Brand
Supervisor, Quality Control CGT (Swing Shift) *PC 1551
Miltenyi Biotec Brand, Gaithersburg, Maryland, us, 20883
Supervisor, Quality Control CGT (Swing Shift) *PC 1551
Job Category
: Manufacturing
Requisition Number
: SUPER003499
Posted : November 19, 2025
Full-Time
On-site
Locations Gaithersburg, MD 1201 Clopper Road Gaithersburg, MD 20878, USA
This position is primarily responsible for the scheduling and coordination of the daily Quality Control activities and GMP release testing. Leading QC team and facilitating training for QC team members.
Essential Duties and Responsibilities
Supervise Quality Control (QC) team, oversees the day-to-day activities including review and approval for QC data, and facilitates training for QC team.
Identify and mitigate risks in QC labs that could negatively impact the safety or quality of the product.
Responsible for the proper maintenance and use of equipment in strict accordance with cGMPs, SOPs and safety policies.
Assist with writing and revising Standard Operating Procedures (SOP).
Prepare protocols or report for prospective new process/equipment for validation and qualification activities.
Coordinate the ordering of supplies and proper waste management.
Coordinate all aspects of incoming samples, sample load, and segregation.
Coordinate assay qualification and validation activities, as relevant.
Support career growth and development for QC team.
Participate and present during scheduled meetings (internal and external), as appropriate.
Lead and perform investigations, as required.
Provide cross-functional support to other departments, as required.
Support other aspects of Quality Control, as qualified and necessary.
Requirements
Bachelor’s (B.S.) or Master’s (M.S.) degree in the life sciences or related concentration from a four‑year college or university, with a minimum of 5 years of experience working in the biotech industry with demonstrated GMP/GLP experience and 0‑2 years' experience in a supervisory role.
Must have strong demonstrated experience building and/or leading QC team. Hands on experience with cell culture and aseptic technique is required.
Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel; reach with hands and arms, talk, and hear. The employee is required to stand; climb or balance and stoop, kneel, crouch. The employee must occasionally lift and/or move up to 20 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Must have ability to handle more than one task at a time and must work at a rapid pace while maintaining attention to detail.
Work Environment Characteristics The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This job is performed in a temperature‑controlled facility without exposure to extreme hot or cold temperatures. Generally, this job is performed in a clean laboratory setting and routinely uses standard equipment such as centrifuges, biosafety cabinets, microscopes, incubators, pipettes and computers. While performing the duties of this job, the employee is frequently exposed to viruses. Employees entering the laboratory must wear appropriate clothing and protective equipment such as lab coats, glasses and gloves. The noise level in the work environment is usually moderate.
Hiring Range The hiring range for this position is expected to fall between $88,100 - $103,650/year, reflecting the range candidates can reasonably expect to be considered for at time of offer, based on factors such as experience, internal equity, and qualifications.
Benefits In addition to your salary, the Company offers a comprehensive benefits package, including health, vision, and dental insurance, as well as a 401(k) plan. All benefits are subject to eligibility requirements. Certain positions may also be eligible for additional compensation such as bonuses or commissions.
Equal Opportunity Employer Miltenyi Biotec is an EO Employer – M/F/Veteran/Disability/Sexual Orientation/Gender Identity. Miltenyi Biotec, Inc. participates in E-Verify. Equal Opportunity Employer. This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
#J-18808-Ljbffr
: Manufacturing
Requisition Number
: SUPER003499
Posted : November 19, 2025
Full-Time
On-site
Locations Gaithersburg, MD 1201 Clopper Road Gaithersburg, MD 20878, USA
This position is primarily responsible for the scheduling and coordination of the daily Quality Control activities and GMP release testing. Leading QC team and facilitating training for QC team members.
Essential Duties and Responsibilities
Supervise Quality Control (QC) team, oversees the day-to-day activities including review and approval for QC data, and facilitates training for QC team.
Identify and mitigate risks in QC labs that could negatively impact the safety or quality of the product.
Responsible for the proper maintenance and use of equipment in strict accordance with cGMPs, SOPs and safety policies.
Assist with writing and revising Standard Operating Procedures (SOP).
Prepare protocols or report for prospective new process/equipment for validation and qualification activities.
Coordinate the ordering of supplies and proper waste management.
Coordinate all aspects of incoming samples, sample load, and segregation.
Coordinate assay qualification and validation activities, as relevant.
Support career growth and development for QC team.
Participate and present during scheduled meetings (internal and external), as appropriate.
Lead and perform investigations, as required.
Provide cross-functional support to other departments, as required.
Support other aspects of Quality Control, as qualified and necessary.
Requirements
Bachelor’s (B.S.) or Master’s (M.S.) degree in the life sciences or related concentration from a four‑year college or university, with a minimum of 5 years of experience working in the biotech industry with demonstrated GMP/GLP experience and 0‑2 years' experience in a supervisory role.
Must have strong demonstrated experience building and/or leading QC team. Hands on experience with cell culture and aseptic technique is required.
Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel; reach with hands and arms, talk, and hear. The employee is required to stand; climb or balance and stoop, kneel, crouch. The employee must occasionally lift and/or move up to 20 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Must have ability to handle more than one task at a time and must work at a rapid pace while maintaining attention to detail.
Work Environment Characteristics The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This job is performed in a temperature‑controlled facility without exposure to extreme hot or cold temperatures. Generally, this job is performed in a clean laboratory setting and routinely uses standard equipment such as centrifuges, biosafety cabinets, microscopes, incubators, pipettes and computers. While performing the duties of this job, the employee is frequently exposed to viruses. Employees entering the laboratory must wear appropriate clothing and protective equipment such as lab coats, glasses and gloves. The noise level in the work environment is usually moderate.
Hiring Range The hiring range for this position is expected to fall between $88,100 - $103,650/year, reflecting the range candidates can reasonably expect to be considered for at time of offer, based on factors such as experience, internal equity, and qualifications.
Benefits In addition to your salary, the Company offers a comprehensive benefits package, including health, vision, and dental insurance, as well as a 401(k) plan. All benefits are subject to eligibility requirements. Certain positions may also be eligible for additional compensation such as bonuses or commissions.
Equal Opportunity Employer Miltenyi Biotec is an EO Employer – M/F/Veteran/Disability/Sexual Orientation/Gender Identity. Miltenyi Biotec, Inc. participates in E-Verify. Equal Opportunity Employer. This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
#J-18808-Ljbffr