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Pharmaceutical Quality Engineer Jobs (NOW HIRING)

Astrix Inc

Quality Engineer (Pharmaceutical)

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 ...

Noven Pharmaceuticals

Quality Engineer

Miami, FL

$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 ...

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 ...

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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 ...

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 ...

Intellectt INC

Quality Engineer

Northfield, IL · On-site

$74K - $96K/yr

We have an urgent opening for a Quality Engineer position based in Northfield, IL or Chicago, IL ... Medical device or pharmaceutical industry experience required * Strong knowledge of 21 CFR Part 820 ...

Stark Pharma Solutions Inc

Quality Engineer

Lafayette, IN · On-site

$69K - $89K/yr

... pharmaceutical, biotechnology, and medical device roles. I came across your profile and wanted to ... Quality Engineer Location: Lafayette, IN Duration: 6-12 Month Contract Job Summary We are seeking a ...

McKesson

Sr Associate Quality Engineer

Louisville, KY

$65K - $109K/yr

The Senior Associate Quality Engineer is responsible for advanced quality oversight across daily ... Critical Skills: * 3-5 years in a pharmaceutical quality/regulatory environment, preferred

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Pharmaceutical Quality Engineer information

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How much do pharmaceutical quality engineer jobs pay per year?

As of Jun 12, 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 quality standards and regulatory requirements. They develop, implement, and monitor quality systems, perform audits, analyze data, and collaborate with production teams to improve product safety and efficacy. Proficiency in GMP, validation, and quality management tools is essential for this role.

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 growth opportunities within the pharmaceutical industry, focusing on ensuring product quality 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 engineers make $500,000?

Senior engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $500,000 or more annually, often through a combination of base salary, bonuses, and stock options. Achieving this level typically requires extensive experience, advanced skills, and working in high-demand industries or leadership roles.

What does QA 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 is essential for maintaining product safety and compliance throughout the production cycle.
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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 99% Full Time, and 1% Nights. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $84,039 per year, or $40.4 per hour.
Quality Engineer (Pharmaceutical)

Quality Engineer (Pharmaceutical)

Astrix Inc

Irvine, CA • On-site

$120K/yr

Full-time

Posted 17 days ago

Job description

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 LA)
Position Overview
We are looking for a Quality Engineer to support quality assurance, process optimization, and regulatory compliance within a regulated manufacturing environment. This role works closely with cross-functional teams to identify quality concerns, improve operational processes, and ensure products consistently meet safety and compliance standards.
Primary Responsibilities
  • Lead investigations into manufacturing deviations and quality issues, including root cause analysis and corrective/preventive actions (CAPA).
  • Monitor and improve quality performance metrics to support continuous improvement initiatives.
  • Create, revise, and maintain SOPs to enhance efficiency and regulatory compliance.
  • Perform risk assessments (FMEA) and assist with implementation of quality-related projects.
  • Manage product specifications, supplier qualification activities, and third-party audits.
  • Coordinate external product certifications such as Halal, Kosher, and NSF.
  • Support recall readiness, mock recalls, and post-market quality monitoring activities.
  • Review new products and formulations to ensure compliance with quality and regulatory standards.
Required Qualifications
  • Bachelor's degree in Biology, Chemical Engineering, or a related scientific discipline.
  • Minimum of 3 years of experience in quality assurance within regulated industries such as pharmaceuticals, medical devices, food, cosmetics, or dietary supplements.
  • Hands-on experience with validation processes, risk management, and quality systems.
  • Strong understanding of cGMP regulations, FDA requirements (21 CFR 111, 117, 210, 211), and ISO 22716 standards.
  • Knowledge of Six Sigma principles and statistical analysis tools.
  • Willingness to travel domestically and internationally when required.

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