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Pharmaceutical Quality Engineer Jobs (NOW HIRING)

Noven Pharmaceuticals

Quality Engineer

Miami, FL · On-site

$68K - $88K/yr

Pharmaceutical Quality System (ICH Q10) * EMA/CHMP/QWP/608924/2014 - Guideline on quality of ... A minimum of a bachelor's degree in science or engineering or associated fields is required.

Noven Pharmaceuticals

Quality Engineer

Miami, FL · On-site

$68K - $88K/yr

Pharmaceutical Quality System (ICH Q10) * EMA/CHMP/QWP/608924/2014 - Guideline on quality of ... A minimum of a bachelor's degree in science or engineering or associated fields is required.

Noven Pharmaceuticals

Quality Engineer

Miami, FL · On-site

$68K - $88K/yr

Develop and maintain quality engineering methodologies, systems, and practices which meet quality ... Pharmaceutical Quality System (ICH Q10) * EMA/CHMP/QWP/608924/2014 - Guideline on quality of ...

Nucleus RadioPharma

Quality Engineer

Rochester, MN · On-site

$100K - $130K/yr

The cGMP Quality Engineer is accountable for ensuring that radiopharmaceutical manufacturing ... Strong attention to detail, problem-solving ability, and knowledge of pharmaceutical quality ...

Stark Pharma Solutions Inc

Quality Engineer

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 ...

Stark Pharma Solutions Inc

Quality Engineer

Newark, NJ · On-site

$75K - $97K/yr

Required Qualifications • Bachelor's Degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, Life Sciences, or a related technical discipline. • 3-5+ years of Quality Engineering ...

LanceSoft Inc

Quality Engineer III

North Haven, CT

$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 ...

kindeva

Supplier Quality Engineer

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 ...

kindeva

Supplier Quality Engineer

Saint Louis, MO

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 ...

kindeva

Supplier Quality Engineer

Saint Louis, MO

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 ...

kindeva

Supplier Quality Engineer

Saint Louis, MO

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 ...

Intellectt INC

Quality Engineer

Chicago, IL · On-site

$74K - $95K/yr

Quality Engineer | Chicago, IL Seeking a Quality Engineer to support a leading medical supply ... Pharmaceuticals, or regulated Healthcare Manufacturing • Strong knowledge of 21 CFR Part 820 and ...

Intellectt INC

Quality Engineer

Plano, TX · On-site

$68K - $89K/yr

We have an urgent opening for a Quality Engineer position based in Texas with one of our ... Experience with combination products (medical device + pharmaceutical components) is highly ...

ATR International

Quality Engineer

Frederick, MD · On-site

$26.28 - $36.28/hr

Demonstrate a deep working knowledge of pharmaceutical relevant standards, principles, and industry best practices. Basic Qualifications * Master's Degree strictly in an Engineering discipline ...

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Pharmaceutical Quality Engineer information

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How much do pharmaceutical quality engineer jobs pay per year?

As of Jul 5, 2026, the average yearly pay for pharmaceutical quality engineer in the United States is $84,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $93,000.00 per year, depending on experience, location, and employer.

What does a Quality Engineer do in the pharmaceutical industry?

A Pharmaceutical Quality Engineer ensures that manufacturing processes and products meet regulatory standards and quality specifications. They develop, implement, and monitor quality systems, perform audits, and analyze data to identify and resolve quality issues, often using tools like GMP and validation protocols. Their role supports compliance with industry regulations such as FDA or EMA requirements.

What is the highest salary in QA Pharma?

The highest salary for a Pharmaceutical Quality Engineer can reach up to $120,000 to $150,000 annually, depending on experience, location, and certifications such as CQE or ASQ. Senior roles or those in highly regulated environments may offer higher compensation, especially with specialized skills in validation, compliance, and quality management systems.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Quality Engineer position, and why are they important?

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.

What is a Pharmaceutical Quality Engineer job?

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).

Is Pharma QA a good career?

A career as a Pharmaceutical Quality Engineer offers stability and opportunities for advancement in the pharmaceutical industry, focusing on ensuring product safety and compliance with regulations. It typically requires knowledge of Good Manufacturing Practices (GMP), quality systems, and relevant certifications, making it a valuable role for those interested in quality assurance and regulatory standards.

What are typical daily responsibilities for a Pharmaceutical Quality Engineer?

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.

What does QA do in pharma?

A Pharmaceutical Quality Engineer is responsible for ensuring that manufacturing processes and products meet quality standards and regulatory requirements. They develop, implement, and monitor quality systems, perform audits, and analyze data to identify and resolve quality issues, often using tools like GMP and validation protocols. Their work helps ensure the safety and efficacy of pharmaceutical products.
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Pharmaceutical Quality Engineer jobs near you
Infographic showing various Pharmaceutical Quality Engineer job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $84,039 per year, or $40.4 per hour.
Quality Engineer - GMP Operations

Quality Engineer - GMP Operations

Dawar Consulting, Inc.

Frederick, MD

$31 - $36/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 8 days ago

Job description

Our client, a world leader 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 Quality Engineering 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:

  • Provide quality oversight for cGMP work orders related to critical equipment, facilities, and utilities.
  • Review and resolve equipment monitoring system (EMS) alarms to ensure uninterrupted manufacturing operations.
  • Support Commissioning, Qualification & Validation (CQV) and Computer System Validation (CSV) activities.
  • Collaborate with Manufacturing, Engineering, Quality Control, Supply Chain, and Product Development teams.
  • Monitor quality metrics, support investigations, and implement quality risk management activities.
  • Ensure compliance with cGMP, FDA regulations, and pharmaceutical quality standards.
  • Support validation, maintenance, calibration, and continuous improvement initiatives.


Qualifications:

  • Bachelor's degree with 2+ years of experience (or equivalent education/experience) in a pharmaceutical or FDA-regulated environment.
  • Experience with cGMP maintenance, calibration, and quality oversight.
  • Familiarity with CMMS systems (e.g., Maximo, BMRAM) and Equipment Monitoring Systems (EMS).
  • Knowledge of CQV, CSV, quality risk management, and GMP compliance.
  • Strong analytical, communication, troubleshooting, and problem-solving skills.


Preferred Qualifications:

  • Experience with Building Management Systems (e.g., Siemens Desigo).
  • Cell & Gene Therapy manufacturing experience is a plus.



If interested, please send us your updated resume at

hr@dawarconsulting.com/akansha@dawarconsulting.com