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 ...
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 ...
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 ...
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 ...
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 ...
Position Summary Quality Engineer II-III, Quality Assurance is responsible for designing ... Knowledge of Pharmaceutical Quality Management Systems requirements and execution * Demonstrated ...
Quick apply
Position Summary Quality Engineer II-III, Quality Assurance is responsible for designing ... Knowledge of Pharmaceutical Quality Management Systems requirements and execution * Demonstrated ...
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 ...
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 ...
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 ...
North Haven, CT · On-site
$71K - $92K/yr
... Pharmaceutical & IT services to a diverse set of customers across various industries around the ... Performs Quality Engineering functions in support of projects associated to product development ...
North Haven, CT · On-site
$71K - $92K/yr
... Pharmaceutical & IT services to a diverse set of customers across various industries around the ... Performs Quality Engineering functions in support of projects associated to product development ...
$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
Cities with the most Afternoon Pharmaceutical Quality Engineer job openings:
The most popular types of Pharmaceutical Quality Engineer jobs are:
States with the most job openings for Afternoon Pharmaceutical Quality Engineer jobs include:
$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
