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Pharmaceutical Quality Engineer Jobs (NOW HIRING)

Quality Engineer

Cambridge, MA ยท 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 ...

Quality Engineer

Newark, NJ ยท 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 ...

Quality Engineer

Ormond Beach, FL ยท On-site

$63K - $81K/yr

Quality Engineer ยท Department: Quality Engineering ยท Location: Ormond Beach, FL (USA) ยท ... Labs, Pharmaceutical Isolators, Biosafety Cabinets, Modular & Mobile Controlled Environments ...

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 ...

Quality Engineer III

North Haven, CT ยท 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 ...

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 ...

Sturtevant, WI Pay Rate: $40-50/hrThis position is responsible for providing Quality Engineering ... Knowledge of quality requirements for medical device / pharmaceutical organization.Strong technical ...

Quality Engineer

Lafayette, IN ยท 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 ...

Sturtevant, WI Pay Rate: $40-50/hrThis position is responsible for providing Quality Engineering ... Knowledge of quality requirements for medical device / pharmaceutical organization.Strong technical ...

Quality Engineer (MN)

Moundsview, MN ยท On-site

$80K - $120K/yr

As a Quality Engineer, you will provide hands-on quality engineering and compliance support to pharmaceutical and medical device manufacturing clients. This role partners with client quality ...

Quality Engineer

El Paso, TX ยท On-site

$34 - $35/hr

Title: Engr 1, Quality Client: Medical Device Manufacturing domain Location: El Paso, TX 79912 ... pharmaceutical, or equivalent industry Required. JOB OVERVIEW This position assists in the ...

Quality Engineer

Buena, NJ ยท On-site

$71K - $92K/yr

QUALITY ENGINEER At Comar, we're passionate about progress and finding opportunity in new ideas. In ... pharmaceutical industry best practices. Identify needs, aid development and presentation of ...

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Quality Engineer

Hayward, CA ยท On-site

$76.54/hr

Title: Quality Engineer (Contract) Pay Rate: $76.54/hour (W-2) plus benefits About the Role: Our ... Source One provides a full range of professionals to the Pharmaceutical & Healthcare, Defense ...

Quality Engineer

San Juan, PR ยท On-site

$70K - $91K/yr

Position Summary The Quality Engineer will support quality and compliance activities within a ... Required experience in the Medical Device or Pharmaceutical industry. * Strong knowledge and ...

Senior Quality Engineer

Englewood, CO ยท On-site

$95K - $121K/yr

The Senior Quality Engineer plays a critical role in ensuring that products and processes meet the ... At Leiters Health, we're not just another pharmaceutical company - we're pioneers in the field ...

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Pharmaceutical Quality Engineer information

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$45K

$84K

$119K

How much do pharmaceutical quality engineer jobs pay per year?

As of Aug 16, 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 is a pharmaceutical quality engineer?

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).

What are the daily responsibilities of 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 skills and qualifications are needed to be a pharmaceutical quality engineer?

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.

Is pharmaceutical quality engineer a good career?

A pharmaceutical quality engineer plays a key role in ensuring the safety and compliance of pharmaceutical products by developing and maintaining quality systems, conducting audits, and working with regulatory standards like GMP. The profession offers strong job stability, competitive salaries, and opportunities for advancement, especially with relevant certifications and technical skills. It is suitable for individuals interested in science, quality assurance, and regulatory compliance within the pharmaceutical industry.

What does a Pharmaceutical Quality Engineer do in the pharmaceutical industry?

A Pharmaceutical Quality Engineer is responsible for developing, implementing, and maintaining quality systems to ensure pharmaceutical products meet safety and efficacy standards. They conduct audits, review manufacturing processes, and ensure compliance with regulatory requirements such as Good Manufacturing Practices (GMP). The role often involves analyzing data, troubleshooting quality issues, and collaborating with cross-functional teams to improve product quality and process efficiency.
More about Pharmaceutical Quality Engineer jobs

What cities are hiring for Pharmaceutical Quality Engineer jobs?

Cities with the most Pharmaceutical Quality Engineer job openings:

What are the most commonly searched types of Pharmaceutical Quality Engineer jobs?

The most popular types of Pharmaceutical Quality Engineer jobs are:

What states have the most Pharmaceutical Quality Engineer jobs?

States with the most job openings for Pharmaceutical Quality Engineer jobs include:

Infographic showing various Pharmaceutical Quality Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $84,039 per year, or $40.4 per hour.

Quality Engineer

Stark Pharma Solutions Inc

Cambridge, MA โ€ข On-site

$78K - $101K/yr

Contractor

Re-posted 6 days ago


Job description

Hi,

My name is Sravani Dasari, and I am a Talent Acquisition Specialist with
Stark Pharma Solutions, specializing in opportunities across the
Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.
I am actively connecting with professionals for current and
upcoming opportunities. If you are open to exploring new roles or would like to
stay informed about relevant positions, please send me your updated resume
along with the best number and time to reach you.
You can also follow Stark Pharma Solutions on LinkedIn for the
latest job updates:
https://www.linkedin.com/company/99455976/

Job Title: Quality Engineer
Location: Cambridge , MA
Industry: 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 Medical Device and Pharmaceutical manufacturing environment. The Quality Engineer will be responsible for maintaining quality systems, supporting investigations, driving continuous improvement initiatives, and ensuring compliance with FDA, cGMP, ISO 13485, and company quality standards. The ideal candidate will work cross-functionally with Manufacturing, Validation, Engineering, and Regulatory teams to ensure product quality and patient safety.

Key Responsibilities

  • Support Quality Management System (QMS) activities and ensure compliance with FDA, cGMP, and ISO 13485 requirements.
  • Review and approve deviations, non-conformances, CAPAs, and change controls.
  • Conduct root cause investigations and implement corrective and preventive actions.
  • Support internal, customer, and regulatory audits and inspections.
  • Review manufacturing, validation, and quality documentation for compliance.
  • Perform risk assessments and quality impact evaluations.
  • Monitor quality metrics and identify opportunities for continuous improvement.
  • Support supplier quality activities, including qualification and performance monitoring.
  • Collaborate with cross-functional teams to ensure quality requirements are met throughout the product lifecycle.
  • Assist in process validation, equipment qualification, and product quality improvement initiatives.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Quality, or a related field.
  • 3+ years of Quality Engineering experience in Medical Device, Pharmaceutical, or Biotechnology industries.
  • Knowledge of FDA regulations, cGMP, ISO 13485, and quality systems.
  • Experience with CAPA, deviations, change control, and investigations.
  • Strong problem-solving and root cause analysis skills.
  • Excellent communication and documentation skills.