... change control, corrective and preventative actions, and assay validation planning to ensure ... In addition, the position is responsible for providing QA support for clinical trial assay ...
... change control, corrective and preventative actions, and assay validation planning to ensure ... In addition, the position is responsible for providing QA support for clinical trial assay ...
Quality Control Analyst
$24.25 - $32.50/hr
Mallinckrodt Pharmaceuticals is a multibillion dollar specialty pharmaceutical company focused on ... TRUSTWORTHY - We consistently model our values The Quality Control (QC) Analyst will work both ...
Quality Control Analyst
$24.25 - $32.50/hr
Mallinckrodt Pharmaceuticals is a multibillion dollar specialty pharmaceutical company focused on ... TRUSTWORTHY - We consistently model our values The Quality Control (QC) Analyst will work both ...
Quality Control Analyst
Madison, WI · On-site
$24.25 - $32.50/hr
Mallinckrodt Pharmaceuticals is a multibillion dollar specialty pharmaceutical company focused on ... TRUSTWORTHY - We consistently model our values The Quality Control (QC) Analyst will work both ...
Quality Control Analyst
Madison, WI · On-site
$24.25 - $32.50/hr
Mallinckrodt Pharmaceuticals is a multibillion dollar specialty pharmaceutical company focused on ... TRUSTWORTHY - We consistently model our values The Quality Control (QC) Analyst will work both ...
Quality Control (QC) Engineer / Analyst
Concord, NC · On-site
$22.25 - $30/hr
We are seeking a Quality Control (QC) professional to support laboratory testing and quality assurance activities within a GMP-regulated pharmaceutical manufacturing environment. This role will focus ...
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Quality Control (QC) Engineer / Analyst
Concord, NC · On-site
$22.25 - $30/hr
We are seeking a Quality Control (QC) professional to support laboratory testing and quality assurance activities within a GMP-regulated pharmaceutical manufacturing environment. This role will focus ...
Quality Control Chemist
$25 - $32/hr
Open (please include requirements with resume) We are a growing OTC contract manufacturer serving the pharmaceutical and personal care industry. This is a hands-on QC role at the center of our ...
Quick apply
Quality Control Chemist
$25 - $32/hr
Open (please include requirements with resume) We are a growing OTC contract manufacturer serving the pharmaceutical and personal care industry. This is a hands-on QC role at the center of our ...
Quality Control Chemist
Yonkers, NY · On-site
$25 - $32/hr
Open (please include requirements with resume) We are a growing OTC contract manufacturer serving the pharmaceutical and personal care industry. This is a hands-on QC role at the center of our ...
Quick apply
Quality Control Chemist
Yonkers, NY · On-site
$25 - $32/hr
Open (please include requirements with resume) We are a growing OTC contract manufacturer serving the pharmaceutical and personal care industry. This is a hands-on QC role at the center of our ...
Quality Control Chemist
$25 - $32/hr
Open (please include requirements with resume) We are a growing OTC contract manufacturer serving the pharmaceutical and personal care industry. This is a hands-on QC role at the center of our ...
Quick apply
Quality Control Chemist
$25 - $32/hr
Open (please include requirements with resume) We are a growing OTC contract manufacturer serving the pharmaceutical and personal care industry. This is a hands-on QC role at the center of our ...
Deviation Investigations Specialist
Davie, FL · On-site
$35/hr
Experience supporting investigations within pharmaceutical manufacturing, engineering, or QC laboratory environments. * Strong knowledge of cGMP regulations, pharmaceutical quality systems, and data ...
Quick apply
Deviation Investigations Specialist
Davie, FL · On-site
$35/hr
Experience supporting investigations within pharmaceutical manufacturing, engineering, or QC laboratory environments. * Strong knowledge of cGMP regulations, pharmaceutical quality systems, and data ...
Quality Control Manager
High Point, NC · On-site
... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...
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Quality Control Manager
High Point, NC · On-site
... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...
Director of Quality (Pharmaceutical Manufacturing)
$125K - $145K/yr
Responsible for the organizational elements of First Priority's Quality Control, Quality Assurance ... Minimum of 10 years of pharmaceutical experience * Must have FDA regulatory knowledge and ...
Director of Quality (Pharmaceutical Manufacturing)
$125K - $145K/yr
Responsible for the organizational elements of First Priority's Quality Control, Quality Assurance ... Minimum of 10 years of pharmaceutical experience * Must have FDA regulatory knowledge and ...
... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...
... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...
Quality Control Manager
High Point, NC · On-site
... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...
Quality Control Manager
High Point, NC · On-site
... Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following ... Quality Control Manager Summary: We are seeking a Quality Control Manager for a 6 month contract to ...
Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
The ideal candidate will bring deep expertise in pharmaceutical quality systems, regulatory ... Change control * Deviations * CAPAs * Document management * Supplier quality * Escalation ...
Quick apply
Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
The ideal candidate will bring deep expertise in pharmaceutical quality systems, regulatory ... Change control * Deviations * CAPAs * Document management * Supplier quality * Escalation ...
Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
The ideal candidate will bring deep expertise in pharmaceutical quality systems, regulatory ... Change control * Deviations * CAPAs * Document management * Supplier quality * Escalation ...
Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
The ideal candidate will bring deep expertise in pharmaceutical quality systems, regulatory ... Change control * Deviations * CAPAs * Document management * Supplier quality * Escalation ...
Academic Worker - Quality (QA/QC)
Elwood, KS · On-site
This role offers a comprehensive introduction to the pharmaceutical quality environment, providing ... Understand and analyze QA/QC workflows to create visual process flows and updated Standard ...
Academic Worker - Quality (QA/QC)
Elwood, KS · On-site
This role offers a comprehensive introduction to the pharmaceutical quality environment, providing ... Understand and analyze QA/QC workflows to create visual process flows and updated Standard ...
Quality Control Supervisor
Jersey Shore, PA · On-site
Manage teams of QC Technicians & Team Leads in execution of QC processes, schedule and personnel to ... Preferably with exposure to medical device, pharmaceutical or related manufacturing environment.
Quality Control Supervisor
Jersey Shore, PA · On-site
Manage teams of QC Technicians & Team Leads in execution of QC processes, schedule and personnel to ... Preferably with exposure to medical device, pharmaceutical or related manufacturing environment.
Director of Quality (Pharmaceutical Manufacturing)
Elgin, IL · On-site
$125K - $145K/yr
Responsible for the organizational elements of First Priority's Quality Control, Quality Assurance ... Minimum of 10 years of pharmaceutical experience * Must have FDA regulatory knowledge and ...
Quick apply
Director of Quality (Pharmaceutical Manufacturing)
Elgin, IL · On-site
$125K - $145K/yr
Responsible for the organizational elements of First Priority's Quality Control, Quality Assurance ... Minimum of 10 years of pharmaceutical experience * Must have FDA regulatory knowledge and ...
Manage teams of QC Technicians & Team Leads in execution of QC processes, schedule and personnel to ... Preferably with exposure to medical device, pharmaceutical or related manufacturing environment.
Manage teams of QC Technicians & Team Leads in execution of QC processes, schedule and personnel to ... Preferably with exposure to medical device, pharmaceutical or related manufacturing environment.
QC Analyst
Miami, FL · On-site
$23 - $30.75/hr
The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on ...
QC Analyst
Miami, FL · On-site
$23 - $30.75/hr
The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on ...
QC Analyst
Miami, FL · On-site
$23 - $30.75/hr
The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on ...
QC Analyst
Miami, FL · On-site
$23 - $30.75/hr
The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on ...
Pharmaceutical Quality Control information
See salary details
$10.82 - $14.42
9% of jobs
$14.42 - $18.03
12% of jobs
$18.80 is the 25th percentile. Wages below this are outliers.
$18.03 - $21.63
22% of jobs
The median wage is $23.44 / hr.
$21.63 - $25.24
16% of jobs
$25.24 - $28.85
9% of jobs
$32.34 is the 75th percentile. Wages above this are outliers.
$28.85 - $32.45
9% of jobs
$32.45 - $36.06
11% of jobs
$36.06 - $39.66
5% of jobs
$39.66 - $43.27
5% of jobs
$43.27 - $46.88
2% of jobs
$46.88 - $50.48
1% of jobs
$10
$27
$50
How much do pharmaceutical quality control jobs pay per hour?
As of Jun 9, 2026, the average hourly pay for pharmaceutical quality control in the United States is $27.14, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $33.65 per hour, depending on experience, location, and employer.
What are some typical daily tasks for someone working in Pharmaceutical Quality Control?
A typical day in Pharmaceutical Quality Control involves performing laboratory tests and analyses on raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with safety and regulatory standards. You may prepare and calibrate lab equipment, document test results, review batch records, and assist in investigations of deviations or out-of-specification findings. Additionally, collaboration with production, research, and quality assurance teams is common to maintain continuous improvement and address any quality issues quickly. This role is detail-oriented and often includes both routine testing and problem-solving activities, making each day varied and impactful.
What are the key skills and qualifications needed to thrive in the Pharmaceutical Quality Control position, and why are they important?
Pharmaceutical Quality Control professionals need a solid background in chemistry, biology, or pharmacy, often supported by a relevant degree and industry knowledge. Familiarity with laboratory instrumentation, Good Manufacturing Practices (GMP), and quality management systems, along with certifications like ASQ or GxP training, is highly beneficial. Attention to detail, strong analytical thinking, and clear communication are key soft skills that drive accuracy and collaboration. These competencies are crucial for ensuring that pharmaceutical products meet strict safety, efficacy, and regulatory standards.
What is a Pharmaceutical Quality Control job?
A Pharmaceutical Quality Control (QC) job involves ensuring that medications meet required safety, efficacy, and quality standards before distribution. Professionals in this field conduct tests, analyze raw materials and finished products, and ensure compliance with regulatory guidelines like Good Manufacturing Practices (GMP). They use analytical techniques such as HPLC, spectroscopy, and microbiological testing. QC specialists also document findings, investigate deviations, and collaborate with other departments to resolve quality issues. Their work helps maintain product integrity and patient safety.
More about Pharmaceutical Quality Control jobs
What cities are hiring for Pharmaceutical Quality Control jobs? Cities with the most Pharmaceutical Quality Control job openings:
What are the most commonly searched types of Pharmaceutical Quality Control jobs? The most popular types of Pharmaceutical Quality Control jobs are:
What states have the most Pharmaceutical Quality Control jobs? States with the most job openings for Pharmaceutical Quality Control jobs include:
What job categories do people searching Pharmaceutical Quality Control jobs look for? The top searched job categories for Pharmaceutical Quality Control jobs are:
Job description
Job Description
Job Description:
The individual in this position is responsible for performing day-to-day quality assurance (QA) activities, managing QA processes such as document management, internal audits, instrumentation change control, corrective and preventative actions, and assay validation planning to ensure compliance to GCLP requirements as the Client Oncology Clinical Research Laboratory (POCRL) develops, validates, and performs clinical trial assays. In addition, the position is responsible for providing QA support for clinical trial assay activities, including receipt, accessioning, and internal tracking of clinical trial biospecimens.
RESPONSIBILITIES:
Maintain, troubleshoot, and monitor the effectiveness of the POCRL's Quality Management System (QMS)
Ensure that POCRL activities conform with the requirements of the laboratory QMS
Coordinate creation, approval, implementation, and periodic reviews of Client Standard Operating Procedures for the POCRL according to GCLP guidelines
Review and approve new assay validation plans and reports according to GCLP guidelines with reference to CAP/CLIA regulations for molecular assay validation
Draft, review and approve continuing quality improvement documentation
Maintain laboratory QMS documentation in Client's document management system
Conduct annual QA audits of the POCRL & clinical trial assay processes, document findings, compose and execute Corrective and Preventative Action Plans as appropriate
Coordinate external QA audits as required and advise laboratory director of appropriate corrective actions
Serve as the POCRL's point of contact with clinical Biomarker Assay Specialist groups withing early- and late-clinical development
Ensure that the maintenance/calibration status of POCRL equipment is monitored and current
TECHNICAL SKILLS:
Ability to create and enforce laboratory standard operating procedures
Knowledge of molecular biology and laboratory safety procedures for handling hazardous chemicals and biosafety level 2 biohazard materials
Knowledge of standard molecular biology laboratory equipment
Excellent written and verbal communication skills
Ability to work independently
Ability to interface with clinical research teams
Proficiency with standard office software (Microsoft Office, Adobe Acrobat)
What is the minimum education experience required?:
BS/MS in a biological science, pharmacy, medical technology, or a related field
Medical Technology, MT (ASCP) license or equivalent (preferred)
At least 2 years' experience working in a laboratory setting that included a QMS
Good working knowledge of GCP/GCLP guidelines
Experience working in a GCP/GCLP environment (preferred)
Additional Information
All your information will be kept confidential according to EEO guidelines.
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996