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Pharmaceutical Qa Manager Jobs (NOW HIRING)

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced ... The QA Specialist will be responsible for implementing and maintaining quality management systems ...

General (8:30 AM - 5:00 PM; flexibility required as per business needs) Reports To: QA Manager Job ... Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related discipline (Master ...

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced ... The QA Specialist will be responsible for implementing and maintaining quality management systems ...

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ... Pharmaceutical Sciences, or related field . * 7+ years of experience in quality assurance within ...

Quality Assurance Manager

Taylor, MS · On-site

$90K - $105K/yr

Manager, Quality Assurance Kelly ® Science & Clinical is seeking a Quality Assurance Manager for a direct hire position with a national pharmaceutical leader at their site in Taylor, MS. If you're ...

Job Title: QA Manager Job Title: Quality Assurance Manager Reports to: Director of Quality ... customers (including pharmaceutical partners), business partners, and third-party vendors.

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Pharmaceutical Qa Manager information

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$24K

$86.2K

$158K

How much do pharmaceutical qa manager jobs pay per year?

As of Jun 16, 2026, the average yearly pay for pharmaceutical qa manager in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 per year, depending on experience, location, and employer.

What does a Pharmaceutical QA Manager do?

A Pharmaceutical QA (Quality Assurance) Manager is responsible for overseeing all aspects of quality assurance within a pharmaceutical company. This includes developing and implementing quality management systems, ensuring compliance with regulatory standards (such as FDA or EMA), and supervising audits and inspections. QA Managers work closely with production, quality control, and regulatory affairs teams to ensure that all products meet strict safety and efficacy standards before reaching the market. Their role is vital in maintaining product integrity and protecting patient safety.

What are the most common challenges faced by a Pharmaceutical QA Manager during regulatory audits?

Pharmaceutical QA Managers often face challenges such as ensuring documentation is consistently accurate and up-to-date, managing cross-functional team preparedness, and addressing any identified gaps in compliance swiftly during regulatory audits. Auditors may request detailed evidence of adherence to Good Manufacturing Practices (GMP) and quality systems, requiring a deep understanding of both internal processes and current regulatory expectations. Proactive communication, regular internal audits, and continuous training are key strategies to overcome these challenges and maintain a state of audit readiness.

What is the difference between Pharmaceutical Qa Manager vs Pharmaceutical Quality Control Analyst?

AspectPharmaceutical Qa ManagerPharmaceutical Quality Control Analyst
CredentialsBachelor's/Master's in Pharmacy, Chemistry, or related field; GMP certification often preferredBachelor's in Chemistry, Pharmacy, or related field; GMP training beneficial
Work EnvironmentOversees quality systems, manages teams, and ensures compliance in manufacturing facilitiesPerforms laboratory testing, analyzes samples, and documents results in QC labs
Employer & Industry UsageUsed in pharmaceutical manufacturing companies, regulatory agencies, and quality assurance departmentsCommonly employed in QC laboratories within pharmaceutical companies and contract labs

The Pharmaceutical Qa Manager focuses on overseeing quality assurance processes, managing teams, and ensuring compliance with regulations. In contrast, the Pharmaceutical Quality Control Analyst primarily conducts laboratory testing and analyzes samples to verify product quality. Both roles require relevant certifications and are integral to maintaining high standards in pharmaceutical production.

What are the key skills and qualifications needed to thrive as a Pharmaceutical QA Manager, and why are they important?

To thrive as a Pharmaceutical QA Manager, you need in-depth knowledge of pharmaceutical regulations, quality assurance processes, and a relevant science degree, often supported by experience in GMP environments. Familiarity with quality management systems (QMS), documentation tools, and certifications such as Six Sigma or ISO 9001 are commonly required. Strong leadership, attention to detail, problem-solving abilities, and effective communication are standout soft skills in this role. These competencies are crucial for ensuring product quality, regulatory compliance, and maintaining the integrity of pharmaceutical operations.
What cities are hiring for Pharmaceutical Qa Manager jobs? Cities with the most Pharmaceutical Qa Manager job openings:
What states have the most Pharmaceutical Qa Manager jobs? States with the most job openings for Pharmaceutical Qa Manager jobs include:
Pharmaceutical - Quality Assurance

Pharmaceutical - Quality Assurance

Integrated Resources INC

San Diego, CA • On-site

Contractor

Posted 3 hours ago


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.


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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