Advanced level degree preferred * 5+ years of Pharmaceutical or Biotechnology industry experience ... QC management experience * Quality leadership experience working on cross-functional teams to ...
Advanced level degree preferred * 5+ years of Pharmaceutical or Biotechnology industry experience ... QC management experience * Quality leadership experience working on cross-functional teams to ...
Manager, Quality Control
Sacramento, CA · On-site
Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next ... The Manager, Quality Control is responsible for providing oversight for the GMP testing of cell ...
Manager, Quality Control
Sacramento, CA · On-site
Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next ... The Manager, Quality Control is responsible for providing oversight for the GMP testing of cell ...
Manager, Quality Control
Bridgewater, NJ · On-site
$90K - $210K/yr
Create/Review and approve quality control operation procedures * Manage the validation of ... biotech environment * At least 2 years in a managerial role * Prior experience related to method ...
Manager, Quality Control
Bridgewater, NJ · On-site
$90K - $210K/yr
Create/Review and approve quality control operation procedures * Manage the validation of ... biotech environment * At least 2 years in a managerial role * Prior experience related to method ...
Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next ... The Manager, Quality Control is responsible for providing oversight for the GMP testing of cell ...
Quick apply
Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next ... The Manager, Quality Control is responsible for providing oversight for the GMP testing of cell ...
Quality Control Manager
Miami, FL · On-site
The Quality Control (QC) Manager is responsible for leading and managing Quality Control laboratory ... biotech, or related) * Strong working knowledge of cGMPs, FDA regulations, and FDA guidance ...
Quality Control Manager
Miami, FL · On-site
The Quality Control (QC) Manager is responsible for leading and managing Quality Control laboratory ... biotech, or related) * Strong working knowledge of cGMPs, FDA regulations, and FDA guidance ...
Quality Control Manager
High Point, NC · On-site
... biotech industry quality control. • 5+ years of people management experience leading QC ... laboratory teams. • Experience managing laboratory investigations, deviations, and CAPA processes ...
Quality Control Manager
High Point, NC · On-site
... biotech industry quality control. • 5+ years of people management experience leading QC ... laboratory teams. • Experience managing laboratory investigations, deviations, and CAPA processes ...
... biotech industry quality control. • 5+ years of people management experience leading QC ... laboratory teams. • Experience managing laboratory investigations, deviations, and CAPA processes ...
... biotech industry quality control. • 5+ years of people management experience leading QC ... laboratory teams. • Experience managing laboratory investigations, deviations, and CAPA processes ...
Quality control manager
Cambridge, MA · On-site
Our Client is looking for Quality Control Manager-with Small molecules, validation, analytical ... biotechnology industry. Experience directing activities related to analytical method development ...
Quality control manager
Cambridge, MA · On-site
Our Client is looking for Quality Control Manager-with Small molecules, validation, analytical ... biotechnology industry. Experience directing activities related to analytical method development ...
Quality Control Scientist
Vacaville, CA · On-site
$20 - $25/hr
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... Our client is a leading biotechnology company that combines technological insight with world-class ...
Quick apply
Quality Control Scientist
Vacaville, CA · On-site
$20 - $25/hr
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... Our client is a leading biotechnology company that combines technological insight with world-class ...
Description The Quality Control (QC) Manager is responsible for ensuring that all installed systems, components, and assemblies meet or exceed customer specifications, project standards, and ...
Description The Quality Control (QC) Manager is responsible for ensuring that all installed systems, components, and assemblies meet or exceed customer specifications, project standards, and ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
Serves as a resource to cGMP facility management in identifying and assessing the appropriate ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
Serves as a resource to cGMP facility management in identifying and assessing the appropriate ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
Serves as a resource to cGMP facility management in identifying and assessing the appropriate ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
$87K - $92K/yr
Serves as a resource to cGMP facility management in identifying and assessing the appropriate ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
The Director, Quality Control will provide strategic leadership in managing a growing team of ... Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ...
The Director, Quality Control will provide strategic leadership in managing a growing team of ... Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ...
QC Inspector
$41K - $66K/yr
This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...
QC Inspector
$41K - $66K/yr
This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...
QC Inspector
$41K - $66K/yr
This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...
QC Inspector
$41K - $66K/yr
This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...
Quality Control Analyst
Vacaville, CA · On-site
$20 - $25/hr
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... Our client is a leading biotechnology company that combines technological insight with world-class ...
Quick apply
Quality Control Analyst
Vacaville, CA · On-site
$20 - $25/hr
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... Our client is a leading biotechnology company that combines technological insight with world-class ...
cGMP Quality Control (QC) Specialist
Los Angeles, CA · On-site
$87K - $92K/yr
Serves as a resource to cGMP facility management in identifying and assessing the appropriate ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
cGMP Quality Control (QC) Specialist
Los Angeles, CA · On-site
$87K - $92K/yr
Serves as a resource to cGMP facility management in identifying and assessing the appropriate ... Bachelor's degree or higher in biotechnology or closely related field. Demonstrated knowledge of ...
QC Analyst
Chapel Hill, NC · On-site
$33.65 - $36.06/hr
Bachelor's degree in Biology, Microbiology, Biochemistry, Biotechnology, Chemistry, or another related life science field OR * 3+ years of relevant Quality Control, Analytical Development, GMP, or ...
QC Analyst
Chapel Hill, NC · On-site
$33.65 - $36.06/hr
Bachelor's degree in Biology, Microbiology, Biochemistry, Biotechnology, Chemistry, or another related life science field OR * 3+ years of relevant Quality Control, Analytical Development, GMP, or ...
QC Inspector
$41K - $66K/yr
This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...
QC Inspector
$41K - $66K/yr
This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...
QC Inspector
Bothell, WA · On-site
$41K - $66K/yr
This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...
QC Inspector
Bothell, WA · On-site
$41K - $66K/yr
This position reports into the Sr. Quality Manager which is part of Quality organization and ... Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or ...
Manager Biotech Quality Control information
See salary details
$30.5K - $39.5K
5% of jobs
$39.5K - $48.5K
5% of jobs
$48.5K - $57.5K
11% of jobs
$60.3K is the 25th percentile. Wages below this are outliers.
$57.5K - $66.5K
13% of jobs
$66.5K - $75.5K
14% of jobs
The median wage is $77.5K / yr.
$75.5K - $84.5K
12% of jobs
$84.5K - $93.5K
13% of jobs
$96.4K is the 75th percentile. Wages above this are outliers.
$93.5K - $102.5K
11% of jobs
$102.5K - $111.5K
7% of jobs
$111.5K - $120.5K
5% of jobs
$120.5K - $129.5K
5% of jobs
$30.5K
$81.3K
$129.5K
How much do manager biotech quality control jobs pay per year?
What is the difference between Manager Biotech Quality Control vs Quality Control Specialist?
| Aspect | Manager Biotech Quality Control | Quality Control Specialist |
|---|---|---|
| Credentials | Bachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE) | Bachelor's in Life Sciences or related field, Quality Certifications preferred |
| Work Environment | Oversees QC teams, manages testing processes, and ensures compliance | Performs testing, data analysis, and reports results |
| Employer & Industry Usage | Biotech companies, pharmaceutical firms, contract labs | Biotech, pharma, and manufacturing sectors |
The Manager Biotech Quality Control typically oversees testing teams and ensures compliance with quality standards, while the Quality Control Specialist focuses on executing tests and analyzing data. Both roles require relevant scientific credentials, but the manager has additional responsibilities in team leadership and process management.
What does a Manager Biotech Quality Control do?
What are the most common challenges faced by a Manager in Biotech Quality Control, and how are they typically addressed?
What are the key skills and qualifications needed to thrive as a Manager Biotech Quality Control, and why are they important?

Key responsibilities
Provide Quality Control oversight of all cGMP testing of raw materials, in process, product release, clean utility, and environmental monitoring testing.
Review and approve all QC related investigations, including deviations, OOS/OOT, and environmental monitoring investigations, with internal and external laboratories.
Manage and develop the professional and technical skills and performance of department members.
PCI Pharma Services rating
6.7
Based on 42 frontline employees who took The Breakroom Quiz
426th of 521 rated manufacturers
Job description
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
This position is responsible for the daily QC oversight of PCI's laboratory functions. This includes all operational and technical activities in delivering quality chemical, biopharmaceutical and microbiologic testing services to our customers. This position oversees core activities such as in process testing and micro testing. The role includes oversight of raw material, in process, and reviewing release testing of GMP products to support our clients, interacting with Clients concerning project specific QC issues, approving department cGMP documents, contributing to cGMP reports, and managing QC staff as necessary to achieve these tasks.
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ESSENTIAL DUTIES AND RESPONSIBILITIES:
- Provides Quality Control oversight of all cGMP testing of raw materials, in process, product release, clean utility and environmental monitoring testing. Review and approve all QC related investigations (deviations, OOS/OOT, EM Investigations, etc.) both with internal and external laboratories
- Maintains good relations and communications with clients as a primary technical interface
- Interact with customers to identify opportunities to improve quality and establish feedback with manufacturing personnel
- Interface with supplier and customer quality representatives concerning problems with quality control and assure that effective corrective action is implemented
- Working with project teams to represent Quality Control, conducting risk assessments and introducing best practices into the Quality Control processes
- Leading customer interaction on all QC related projects including routine testing updates
- Manage and develop professional and technical skills and performance of department members
- Assure all QC functions and testing are being performed according to FDA, EMA, ICH and other international regulations, as deemed necessary
- Supporting regulatory information requests from customers as it pertains to QC. Supporting Operations, Project Management Staff and Quality Assurance as needed
- Drive technical troubleshooting, operational improvements, and efficiency improvements while working within cGMP and global regulatory compliance
- Demonstrate substantial knowledge of subject matter, industry best practices and trends
- Other tasks as assigned by management.
QUALIFICATIONS:
Required:
- BS in Chemistry, Biochemistry, Microbiology, Biology or related life sciences field. Advanced level degree preferred
- 5+ years of Pharmaceutical or Biotechnology industry experience
- Experience in leading a commercial, aseptic drug product quality control team,
- 5+ years previous QC management experience
- Quality leadership experience working on cross-functional teams to harmonize operational, testing and compliance processes
- Experience in the Management of +5 people
Preferred:
- Prior experience in a CMO or dealing with CMOs preferred
- Demonstrates excellent verbal, written, and interpersonal communication skills
- Demonstrated ability to perform in a fast-paced environment
- Highly developed leadership capabilities to motivate and inspire teams
- Independently motivated, detail oriented and good problem-solving ability.
- Demonstrates a strong customer service orientation with effective follow through
- Driven to excellence while encouraging others to engage in process improvement and innovation
- A leader who inspires and motivates, through excellent listening skills and a willingness to mentor team members
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Join us and be part of building the bridge between life changing therapies and patients. Let's talk future
Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
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