Frederick, MD · On-site
$70 - $85/hr
Quality Engineer - GMP Operations Frederick, United States | Posted on 06/26/2026 Our client, a ... Ensure compliance with cGMP, FDA regulations, and pharmaceutical quality standards. * Support ...
Frederick, MD · On-site
$70 - $85/hr
Quality Engineer - GMP Operations Frederick, United States | Posted on 06/26/2026 Our client, a ... Ensure compliance with cGMP, FDA regulations, and pharmaceutical quality standards. * Support ...
Irvine, CA · On-site
$120K/yr
Pay Rate Low: 100000 | Pay Rate High: 120000 Opportunity to join a rapidly growing pharmaceutical organization in a highly impactful Quality Engineer capacity. Salary: $100-120k/yr Hybrid (Irvine OR ...
Irvine, CA · On-site
$120K/yr
Pay Rate Low: 100000 | Pay Rate High: 120000 Opportunity to join a rapidly growing pharmaceutical organization in a highly impactful Quality Engineer capacity. Salary: $100-120k/yr Hybrid (Irvine OR ...
Philadelphia, PA · On-site
$72K - $93K/yr
Pharmaceutical Quality Engineer Consultant Location: Southern New Jersey Work Arrangement: Onsite Duration: 6-7 months Start: Early October Schedule: 24-40 hours per week Travel: Local candidates ...
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Philadelphia, PA · On-site
$72K - $93K/yr
Pharmaceutical Quality Engineer Consultant Location: Southern New Jersey Work Arrangement: Onsite Duration: 6-7 months Start: Early October Schedule: 24-40 hours per week Travel: Local candidates ...
Cambridge, MA · On-site
$78K - $101K/yr
Medical Device / Pharmaceutical Job Summary We are seeking a highly motivated and detail-oriented Quality Engineer to support quality assurance and compliance activities within a GMP-regulated ...
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Cambridge, MA · On-site
$78K - $101K/yr
Medical Device / Pharmaceutical Job Summary We are seeking a highly motivated and detail-oriented Quality Engineer to support quality assurance and compliance activities within a GMP-regulated ...
$36 - $41/hr
Job Title: Quality Engineer The Quality Engineer will maintain and improve quality systems ... Experience in regulated industries such as medical devices, aerospace, pharmaceuticals, or ...
New
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$36 - $41/hr
Job Title: Quality Engineer The Quality Engineer will maintain and improve quality systems ... Experience in regulated industries such as medical devices, aerospace, pharmaceuticals, or ...
New
Newark, NJ · On-site
$75K - $97K/yr
Bachelor's Degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, Life Sciences, or a related technical discipline. * 3-5+ years of Quality Engineering, Quality Assurance, Validation, or ...
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Newark, NJ · On-site
$75K - $97K/yr
Bachelor's Degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, Life Sciences, or a related technical discipline. * 3-5+ years of Quality Engineering, Quality Assurance, Validation, or ...
Position Summary Quality Engineer II-III, Quality Assurance is responsible for designing ... Knowledge of Pharmaceutical Quality Management Systems requirements and execution * Demonstrated ...
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Position Summary Quality Engineer II-III, Quality Assurance is responsible for designing ... Knowledge of Pharmaceutical Quality Management Systems requirements and execution * Demonstrated ...
Durham, NC · On-site
$90 - $120/hr
Position Summary Quality Engineer II-III, Quality Assurance is responsible for designing ... Knowledge of Pharmaceutical Quality Management Systems requirements and execution * Demonstrated ...
Durham, NC · On-site
$90 - $120/hr
Position Summary Quality Engineer II-III, Quality Assurance is responsible for designing ... Knowledge of Pharmaceutical Quality Management Systems requirements and execution * Demonstrated ...
Position Summary Quality Engineer II-III, Quality Assurance is responsible for designing ... Knowledge of Pharmaceutical Quality Management Systems requirements and execution * Demonstrated ...
Position Summary Quality Engineer II-III, Quality Assurance is responsible for designing ... Knowledge of Pharmaceutical Quality Management Systems requirements and execution * Demonstrated ...
Saint Louis, MO · On-site
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
Saint Louis, MO · On-site
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
El Paso, TX · On-site
$65K - $84K/yr
Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...
Saint Louis, MO · On-site
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
Saint Louis, MO · On-site
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...
$45K - $51.7K
1% of jobs
$51.7K - $58.5K
3% of jobs
$58.5K - $65.2K
7% of jobs
$65.2K - $71.9K
13% of jobs
$72.2K is the 25th percentile. Wages below this are outliers.
$71.9K - $78.6K
18% of jobs
The median wage is $81.4K / yr.
$78.6K - $85.4K
19% of jobs
$90.9K is the 75th percentile. Wages above this are outliers.
$85.4K - $92.1K
17% of jobs
$92.1K - $98.8K
9% of jobs
$98.8K - $105.5K
6% of jobs
$105.5K - $112.3K
4% of jobs
$112.3K - $119K
2% of jobs
$45K
$84K
$119K
A Pharmaceutical Quality Engineer ensures that pharmaceutical manufacturing processes, products, and systems comply with regulatory standards and quality requirements. They develop and implement quality control procedures, conduct audits, and troubleshoot production issues to maintain compliance. Their role involves working closely with cross-functional teams to improve product quality and efficiency. They also analyze data, oversee validation processes, and ensure adherence to Good Manufacturing Practices (GMP).
Pharmaceutical Quality Engineers typically spend their days performing process validations, analyzing production data, and conducting root cause investigations of quality issues. They collaborate closely with manufacturing, laboratory, and regulatory teams to ensure products comply with internal standards and external regulations. The role often involves writing and reviewing documentation, supporting audits, and recommending improvements to manufacturing processes. This position blends hands-on problem-solving with cross-functional communication, making it both dynamic and impactful on the overall quality and safety of pharmaceutical products.
To thrive as a Pharmaceutical Quality Engineer, you need a solid background in quality assurance, problem-solving, and process improvement, often supported by a degree in engineering, pharmacy, or a related scientific field. Familiarity with regulatory standards (such as GMP, FDA, or ISO 9001), validation software, and quality management systems (QMS) is essential, and certifications like Six Sigma or ASQ CQE can be advantageous. Attention to detail, strong communication, and collaboration skills are crucial for effective cross-functional teamwork and continuous quality improvement. These skills ensure products consistently meet strict regulatory standards for safety and efficacy while supporting efficient and compliant manufacturing operations.
Cities with the most Pharmaceutical Quality Engineer job openings:
The most popular types of Pharmaceutical Quality Engineer jobs are:
States with the most job openings for Pharmaceutical Quality Engineer jobs include:
The top searched job categories for Pharmaceutical Quality Engineer jobs are:
$70 - $85/hr
Other
Medical, Dental, Vision, Retirement
Posted 4 days ago
Frederick, United States | Posted on 06/26/2026
Our client, a worldleader in biotechnology and gene therapy, is looking for a “Quality Engineer - GMP Operations” based in Frederick, MD.
Job Duration: Long Term Contract (Possibility Of Extension)
Pay Rate: $36/hr on W2
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K
Provide QualityEngineering oversight for cGMP maintenance, validation, and equipment monitoring activities supporting commercial and clinical manufacturing. Ensure compliance with regulatory requirements by reviewing work orders, supporting qualification and validation activities, managing quality risks, and collaborating with cross‑functional teams to maintain reliable facility, utility, and equipment performance.
Key Responsibilities
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It services
11 - 50 Employees
Newark, CA, US
2009
