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Pharmaceutical Quality Engineer Jobs (NOW HIRING)

TOMZ Corporation

Quality Engineer

Big Lake, MN

$38.46 - $52.88/hr

Summary of Position: Reporting to the Quality Engineering Manager, this position will be ... Pharmaceutical, etc.). Physical Requirements: * Ability to bend, stoop, squat, kneel, and lift up ...

LHH US

Quality Engineer

Champaign, IL

$80K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience in medical device or pharmaceutical manufacturing environments. * FDA/cGMP knowledge. * Validation experience (IQ/OQ/PQ). * ASQ Certified Quality Engineer (CQE) and/or Six Sigma Green Belt ...

New

SaniSure LLC

Quality Engineer - Complaints

Camarillo, CA · On-site

$95K - $105K/yr

S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they ... Job Summary The Quality Engineer works closely with Operations, Manufacturing Engineering, R&D, ...

Teledyne FLIR LLC

Quality Engineer

Oak Ridge, TN · On-site

$68K - $88K/yr

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. Quality Engineer - PCBA & Electro-Mechanical Systems Join ...

Comar

Quality Engineer

Buena, NJ · On-site

$71K - $92K/yr

  • Medical

  • Dental

  • Retirement

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

New

LHH US

Quality Engineer

Champaign, IL · On-site

$80K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience in medical device or pharmaceutical manufacturing environments. * FDA/cGMP knowledge. * Validation experience (IQ/OQ/PQ). * ASQ Certified Quality Engineer (CQE) and/or Six Sigma Green Belt ...

New

Actalent

Quality Engineer

New Cumberland, PA

$42 - $55/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality assurance experience in a regulated pharmaceutical or biotechnology environment ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

August Bioservices

Quality Engineer

Nashville, TN

$69K - $89K/yr

... role in the global pharmaceutical industry. Our work is instrumental in helping to develop ... The Quality Engineer is responsible for supporting incoming new client projects from the Quality ...

Teledyne FLIR LLC

Quality Engineer

Montgomeryville, PA · On-site

$70K - $91K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the ... Support the development of training to build quality awareness. * Interface with Engineering ...

August Bioservices

Quality Engineer

Nashville, TN · On-site

$69K - $89K/yr

... role in the global pharmaceutical industry. Our work is instrumental in helping to develop ... The Quality Engineer is responsible for supporting incoming new client projects from the Quality ...

August Bioservices

Quality Engineer

Nashville, TN

$69K - $89K/yr

... role in the global pharmaceutical industry. Our work is instrumental in helping to develop ... The Quality Engineer is responsible for supporting incoming new client projects from the Quality ...

DivIHN Integration Inc

Quality Engineer I

Durham, NC · On-site

$69K - $89K/yr

Minimum of 2 years of manufacturing quality engineering experience (preferably in a regulated industry such as health care, medical device, pharmaceutical, etc). Desired Experience/Qualifications:

Teledyne

Quality Engineer

Montgomeryville, PA

$70K - $91K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... pharmaceutical research. We are looking for individuals who thrive on making an impact and want the ... Support the development of training to build quality awareness. * Interface with Engineering ...

Hitachi, Ltd.

Quality Engineer

Michigan City, IN · On-site

$70K - $90K/yr

... pharmaceuticals and cutting edge semi-conductor chips. Our portable compressors provide the air ... The Quality Engineer serves as the primary liaison between the organization and the quality ...

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All JobsPharmaceutical Quality Engineer Jobs

Pharmaceutical Quality Engineer information

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How much do pharmaceutical quality engineer jobs pay per year?

As of Aug 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 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.

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.

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.
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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:
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Pharmaceutical Quality Engineer jobs near you
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

TOMZ Corporation

Big Lake, MN

$38.46 - $52.88/hr

Full-time

Re-posted 28 days ago

Job description

Summary of Position:

Reporting to the Quality Engineering Manager, this position will be responsible for the activities associated with Quality Design & Development (QD&D) Control and Assurance during Product Development Process (PDP) activities as well as continuation design & development support for sustaining manufacturing and product distribution.

Essential Functions:

  • Develop and execute Quality Plans for Quality Product Design and Development projects.
  • Collaborate with engineering teams to initiate and support the development and updates of Risk Management documentation in accordance with project requirements.
  • Establish severity and risk-based Process Master Validation Plan strategies with appropriate V&V rationales.
  • Support operational and process qualifications for customer manufacturing processes in collaboration with engineering teams.
  • Drive Test Method development with Operational and Business considerations and execution of Test Method Validations to measure effectiveness.
  • Implement inspection plans for Incoming, In-Process and Final Product.
  • Develop and justify appropriate sampling plans with characterization of test and inspection methods.
  • Represent Quality Engineering in design reviews.
  • Support initial qualification audit activities for Customer and Regulatory Agencies.
  • Support qualification activities related to supplier and vendor design characterization requirements for projects, including conducting audits and assessments.
  • Support Quality Best Practices and contribute to continuous improvement in GDP/GMP.
  • Apply sound, systematic problem-solving methods in identifying, prioritizing, communicating, and resolving quality issues.
  • Ensure that all site personnel comply with the site-level Quality Management System and training requirements.
  • Support the development of Quality Agreements for external customers.
  • Adhere to the TOMZ Quality Management System.
  • Perform other duties as assigned.

Qualifications:

  • Advanced Post-Secondary Education, Training or Certification coursework.
  • Knowledge of statistical techniques to analyze process capability.
  • Quality certification(s) (e.g., ASQ CQE, QCI, etc.).
  • Skilled in First Article Inspections and Component Qualifications.
  • Knowledge and experience with external standards: ISO 900/9001, ISO 13485, and 21CFR 820, EU MDR, pertaining to product development, design controls, good manufacturing practices, supplier qualification, auditing, quality control (GD&T, Nonconforming Materials, MRB), Corrective and Preventive Actions, and customer complaints).
  • Experience in effectively supporting audits by customers and external regulatory agencies.
  • Strong verbal and written English language communication skills.
  • Successfully meet TOMZ-specific positional and functional on-the-job training requirements.
  • Proficiency with Microsoft Office.
  • A self-starter capable of working independently and as part of a team, with the ability to collaborate across various functional areas, including R&D, Manufacturing, and QA, to achieve results.

Education:

  • Minimum 4-Year degree or equivalent of directly transferrable industry work experience (Engineering or Quality discipline preferred).

Experience:

  • Minimum of 2-5 years’ experience in a regulated manufacturing environment.
  • Experience in Class I, II, and/or III medical device manufacturing within a regulated environment (e.g., Aerospace, Defense, Pharmaceutical, etc.).

Physical Requirements:

  • Ability to bend, stoop, squat, kneel, and lift up to 50 pounds. Team lift or mechanical assistance required for objects over 50 pounds.

  • Ability to sit for prolonged periods.

  • Exposure to oil, grease, occupational noise, cleaning solvents, dust, metal particles, sparks, coolant, and sharp-edged materials. Personal protective equipment (PPE) such as safety glasses, dust masks, ear plugs, cut-resistant or chemical-resistant gloves, and engineering controls may be required.

  • Perform keyboard entries with frequent operation of a computer.

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About TOMZ

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

51 - 200 Employees

Headquarters location

Berlin, CT, US

Year founded

1988

Social media

Facebook

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