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 ...
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 ...
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 ...
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 ...
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 ...
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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 ...
Quality Manager
Deerfield, IL · On-site
$50 - $65/hr
The role involves managing regulatory intelligence activities, supporting document control ... Prior experience in pharmaceutical quality systems and proficiency with Veeva are essential.
Quality Manager
Deerfield, IL · On-site
$50 - $65/hr
The role involves managing regulatory intelligence activities, supporting document control ... Prior experience in pharmaceutical quality systems and proficiency with Veeva are essential.
Why this role matters The Manager, Quality & Pharmaceutical Affairs (MQPA) position will support the Quality and Regulatory Compliance of existing commercialized product portfolios: Dietary ...
Why this role matters The Manager, Quality & Pharmaceutical Affairs (MQPA) position will support the Quality and Regulatory Compliance of existing commercialized product portfolios: Dietary ...
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 ...
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 ...
QA Product Manager
Florham Park, NJ · On-site
Overview The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...
QA Product Manager
Florham Park, NJ · On-site
Overview The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...
The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...
The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...
QA Product Manager
Florham Park, NJ · On-site
Overview The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...
QA Product Manager
Florham Park, NJ · On-site
Overview The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...
Quality Manager
Little Rock, AR · On-site
Join My Medical Supply, a leading pharmaceutical warehouse distribution facility committed to ... We are seeking a dedicated and detail-oriented Quality Manager to oversee our quality assurance ...
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Quality Manager
Little Rock, AR · On-site
Join My Medical Supply, a leading pharmaceutical warehouse distribution facility committed to ... We are seeking a dedicated and detail-oriented Quality Manager to oversee our quality assurance ...
Director, Quality Assurance (Quality Systems)
Fort Lauderdale, FL · On-site +1
$2/hr
... Management System (eQMS) for the Drug division. This role will serve as the primary interface and administrator for the Pharmaceutical Quality System (PQS) at Syncromune, with responsibility for ...
Director, Quality Assurance (Quality Systems)
Fort Lauderdale, FL · On-site +1
$2/hr
... Management System (eQMS) for the Drug division. This role will serve as the primary interface and administrator for the Pharmaceutical Quality System (PQS) at Syncromune, with responsibility for ...
... Management System (eQMS) for the Drug division. This role will serve as the primary interface and administrator for the Pharmaceutical Quality System (PQS) at Syncromune, with responsibility for ...
Quick apply
... Management System (eQMS) for the Drug division. This role will serve as the primary interface and administrator for the Pharmaceutical Quality System (PQS) at Syncromune, with responsibility for ...
Sr. Mgr, Commercial Quality Assurance, US
$150K - $185K/yr
Sr. Manager, Commercial Quality Assurance, US The salary range for this position is between $150k ... Ensure all distribution, storage, and commercialization activities for pharmaceutical products ...
Sr. Mgr, Commercial Quality Assurance, US
$150K - $185K/yr
Sr. Manager, Commercial Quality Assurance, US The salary range for this position is between $150k ... Ensure all distribution, storage, and commercialization activities for pharmaceutical products ...
Bilingual Quality Assurance Line Inspector I - Pharmaceutical Manufacturing Location: Miramar, FL ... Work closely with Operations and Management teams to support quality initiatives. * Maintain ...
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Bilingual Quality Assurance Line Inspector I - Pharmaceutical Manufacturing Location: Miramar, FL ... Work closely with Operations and Management teams to support quality initiatives. * Maintain ...
The position works closely with Medical Directors, Pharmacists, data analytics and the care ... Work with Quality Care Managers on overarching goals and best practices from multiple contracts
The position works closely with Medical Directors, Pharmacists, data analytics and the care ... Work with Quality Care Managers on overarching goals and best practices from multiple contracts
Sr. Mgr, Commercial Quality Assurance, US
Morristown, NJ · On-site
$150K - $185K/yr
Implement, maintain, and continuously improve Grünenthal's Pharmaceutical Quality System within ... Manage relationships with external partners, including 3PLs, wholesalers, and distributors ...
Sr. Mgr, Commercial Quality Assurance, US
Morristown, NJ · On-site
$150K - $185K/yr
Implement, maintain, and continuously improve Grünenthal's Pharmaceutical Quality System within ... Manage relationships with external partners, including 3PLs, wholesalers, and distributors ...
Associate Quality Manager, Stability
Cary, IL · On-site
$112K - $188K/yr
Deep expertise in pharmaceutical stability testing aligned with ICH and global regulatory standards, supported by comprehensive knowledge of diverse analytical techniques and instrumentation.
Associate Quality Manager, Stability
Cary, IL · On-site
$112K - $188K/yr
Deep expertise in pharmaceutical stability testing aligned with ICH and global regulatory standards, supported by comprehensive knowledge of diverse analytical techniques and instrumentation.
Associate Quality Manager, Stability
Cary, IL · On-site
$112K - $188K/yr
Deep expertise in pharmaceutical stability testing aligned with ICH and global regulatory standards, supported by comprehensive knowledge of diverse analytical techniques and instrumentation.
Associate Quality Manager, Stability
Cary, IL · On-site
$112K - $188K/yr
Deep expertise in pharmaceutical stability testing aligned with ICH and global regulatory standards, supported by comprehensive knowledge of diverse analytical techniques and instrumentation.
Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
Quality systems and auditing ... Risk management principles * Pharmaceutical manufacturing operations * Experience supporting API ...
Quick apply
Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
Quality systems and auditing ... Risk management principles * Pharmaceutical manufacturing operations * Experience supporting API ...
Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
Quality systems and auditing ... Risk management principles * Pharmaceutical manufacturing operations * Experience supporting API ...
Director, Quality Compliance (DEA & FDA)
$180K - $220K/yr
Quality systems and auditing ... Risk management principles * Pharmaceutical manufacturing operations * Experience supporting API ...
Pharmaceutical Quality Manager information
See salary details
$24K - $36.2K
12% of jobs
$44.2K is the 25th percentile. Wages below this are outliers.
$36.2K - $48.4K
20% of jobs
$48.4K - $60.5K
14% of jobs
The median wage is $64.6K / yr.
$60.5K - $72.7K
13% of jobs
$72.7K - $84.9K
9% of jobs
$84.9K - $97.1K
5% of jobs
$104.7K is the 75th percentile. Wages above this are outliers.
$97.1K - $109.3K
4% of jobs
$109.3K - $121.5K
4% of jobs
$121.5K - $133.6K
2% of jobs
$133.6K - $145.8K
0% of jobs
$145.8K - $158K
17% of jobs
$24K
$86.2K
$158K
How much do pharmaceutical quality manager jobs pay per year?
What is the difference between Pharmaceutical Quality Manager vs Quality Assurance Specialist?
| Aspect | Pharmaceutical Quality Manager | Quality Assurance Specialist |
|---|---|---|
| Credentials | Typically requires a Bachelor's degree in Pharmacy, Chemistry, or related field; often holds certifications like ASQ CQE or ISO auditor | Usually holds a Bachelor's degree in Life Sciences or related; may also have certifications like ASQ CQPA or ISO auditor |
| Work Environment | Manages quality teams, oversees quality systems, and ensures compliance across manufacturing facilities | Performs audits, reviews documentation, and supports quality processes within labs or production lines |
| Employer & Industry Usage | Commonly employed in pharmaceutical manufacturing, biotech, and healthcare companies | Found in pharmaceutical, biotech, and medical device industries, often within quality departments |
The Pharmaceutical Quality Manager focuses on leading quality management systems and strategic oversight, while the Quality Assurance Specialist handles day-to-day quality checks and documentation. Both roles are essential for ensuring product compliance and safety in the pharmaceutical industry.
How much does a QA manager make at Novartis?
What is the salary of a QA manager?
What are some common challenges faced by Pharmaceutical Quality Managers, and how can they be addressed?
What are the key skills and qualifications needed to thrive as a Pharmaceutical Quality Manager, and why are they important?
What is the role of a pharmaceutical quality manager?
What is the highest salary in QA Pharma?
What does a Pharmaceutical Quality Manager do?

Full-time
Medical, Dental, Vision, PTO
Re-posted 25 days ago
Job description
Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical development and testing processes. The QA Specialist will be responsible for implementing and maintaining quality management systems, conducting inspections and audits, reviewing documentation, and ensuring all activities adhere to regulatory standards, including FDA, DEA, and ISO 17025 requirements. This role requires close collaboration with the development and testing teams to maintain compliance with the regulatory requirements.
Key Responsibilities:
- Ensure adherence to pharmaceutical GMP regulations and internal quality standards.
- Conduct routine and for-cause internal audits and inspections of chemistry, microbiology, and molecular biology laboratories.
- Review and approve GMP-related documentation, including test results, technical reports, investigation reports, and SOPs.
- Coordinate with cross-functional teams to address non-conformities and implement corrective and preventive actions (CAPAs).
- Support regulatory inspections and manage responses to audit findings.
- Monitor quality metrics and report on compliance status.
- Provide training and guidance on GMP requirements to laboratory personnel.
Education & Experience:
- Bachelor's degree in Chemistry or Microbiology.
- Minimum 10 years of experience in pharmaceutical quality assurance with strong knowledge of GMP regulations.
- Experience working within the FDA, DEA, and ISO 17025.
- Proven ability to conduct audits and manage quality documentation.
- Strong communication, analytical, and interpersonal skills.
Requirements
Education:
- Bachelor's degree in Chemistry or Microbiology.
Experience:
- 10 + years of experience in pharmaceutical quality assurance or GMP compliance.
- Familiarity with the FDA, DEA, and the iSO 17025 regulations and requirements.
- Experience in conducting audits and managing quality systems.
Skills:
- Strong analytical and problem-solving abilities.
- Excellent communication and interpersonal skills.
- Ability to work collaboratively in cross-functional teams.
Benefits
- Health Care Plan (Medical, Dental & Vision)
- Paid Time Off (Vacation, Sick & Public Holidays)
- Training & Development
About Synergy BIS
Sourced by ZipRecruiter
Company size
501 - 1,000 Employees
Headquarters location
Reston, VA, US
Year founded
2005