ZipRecruiter

Log In

1

Pharmaceutical Quality Engineer Jobs (NOW HIRING)

Ultimate Solutions

Quality Engineer

San Juan, PR

$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 ...

Leiters Inc

Senior Quality Engineer

Englewood, CO · On-site

$95K - $121K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

atrion

Quality Engineer

Davie, FL

$66K - $85K/yr

A minimum of 10 years of experience in a quality engineering role in regulated industry experience such as medical device or pharmaceutical is required. A minimum of 5 years' experience in the ...

SaniSure LLC

Quality Engineer

Twinsburg, OH · On-site

$80K - $90K/yr

S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they ... Job Summary The Quality Engineer ensures that products manufactured at the Twinsburg, OH facility ...

CYNET SYSTEMS

Quality Engineer II

Scarborough, ME · On-site

$45/hr

Minimum 3+ years of experience in quality engineering within a regulated environment (medical device, pharmaceutical, or similar). * Hands-on experience with product risk management, including hazard ...

AA2IT

Senior Validation Quality Engineer

Sturtevant, WI · On-site

$40 - $50/hr

Minimum Requirements For Validation Quality Engineer Bachelor's Degree Physical Science or Engineering, or equivalent experience. 2+ years Minimum in Medical Device or Pharmaceutical Industry or ...

Merck Group

Quality Engineer

Jaffrey, NH · On-site

$67K - $101K/yr

  • Medical

  • Retirement

  • PTO

... pharmaceutical, biotechnology, or medical device) manufacturing setting with proven track record of successful performance. * Working Knowledge of ISO & FDA regulations (such as ISO 9001, ISO 13485 ...

AA2IT

Senior Validation Quality Engineer

Sturtevant, WI · On-site

$40 - $50/hr

Minimum Requirements For Validation Quality Engineer Bachelor's Degree Physical Science or Engineering, or equivalent experience. 2+ years Minimum in Medical Device or Pharmaceutical Industry or ...

The Goodkind Co

Quality Engineer

Round Rock, TX · On-site

$67K - $86K/yr

The Quality Engineer supports continuous improvement initiatives by analyzing trends, identifying ... Experience in OTC, pharmaceutical, cosmetic, or personal care manufacturing * Experience with ...

The Goodkind Co

Quality Engineer

Round Rock, TX · On-site

$67K - $86K/yr

The Quality Engineer supports continuous improvement initiatives by analyzing trends, identifying ... Experience in OTC, pharmaceutical, cosmetic, or personal care manufacturing * Experience with ...

Mission Critical Group

Quality Engineer

Abilene, TX · On-site

$69K - $90K/yr

... oil & gas, pharmaceuticals, semiconductors, and industrial facilities where uptime is non ... The Quality Engineer is responsible for ensuring that products, processes, and systems meet the ...

Abbott

Quality Engineer II

Scarborough, ME · On-site

$73K - $94K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Minimum 3 years of experience in quality engineering within a regulated environment (medical device, pharmaceutical, or similar) * Hands-on experience with product risk management, including hazard ...

Abbott

Quality Engineer II

Scarborough, ME · On-site

$73K - $94K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Minimum 3 years of experience in quality engineering within a regulated environment (medical device, pharmaceutical, or similar) * Hands-on experience with product risk management, including hazard ...

Abbott

Quality Engineer II

Scarborough, ME · On-site

$73K - $94K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Minimum 3 years of experience in quality engineering within a regulated environment (medical device, pharmaceutical, or similar) * Hands-on experience with product risk management, including hazard ...

Aptar Group

Quality Engineer

Eatontown, NJ · On-site

$72K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Opportunity - Quality Engineer Who we are At Aptar, we use insights, design, engineering and ... pharmaceutical); working knowledge of ISO 9001 (or similar regulation like ISO 13485) * Must ...

Teledyne

Quality Engineer

Oak Ridge, TN

$68K - $88K/yr

... medical imaging and 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 ...

Aptar Group

Quality Engineer

Eatontown, NJ · On-site

$72K - $93K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Opportunity - Quality Engineer Who we are At Aptar, we use insights, design, engineering and ... pharmaceutical); working knowledge of ISO 9001 (or similar regulation like ISO 13485) * Must ...

TOMZ Manufacturing Corp

Quality Engineer

Big Lake, MN · On-site

$80K - $110K/yr

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 ...

previous pagenext page

Showing results 21-40

All JobsPharmaceutical Quality Engineer Jobs

Pharmaceutical Quality Engineer information

See salary details

$45K

$84K

$119K

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.
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:
What job categories do people searching Pharmaceutical Quality Engineer jobs look for? The top searched job categories for Pharmaceutical Quality Engineer jobs are:
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

Ultimate Solutions

San Juan, PR

$70K - $91K/yr

Full-time

Posted 5 days ago

Job description

About Ultimate Solutions Corp.

Ultimate Solutions Corp. is a global leader in compliance and technology solutions, specializing in end-to-end integrated services for the Life Sciences industry. With over 20 years of experience, we have built core competencies by combining regulatory and quality expertise with advanced packaging automation, serialization, brand protection, and IT services. This unique blend of capabilities has enabled us to successfully support clients worldwide.

Position Summary

The Quality Engineer will support quality and compliance activities within a regulated Medical Device environment. This role is responsible for equipment (testing) validations, test method validations, documentation review and approval, and support of quality investigations and CAPAs. The candidate will apply Quality Engineering principles and Six Sigma / Lean tools to drive continuous improvement and implement system or process modifications.

Responsibilities

  • Execute equipment (testing) validations in a Medical Device environment, including protocol development, execution, and final reports.

  • Perform and support test method validations to ensure compliance with intended use and regulatory requirements.

  • Support and/or lead quality investigations, including deviations, nonconformances, root cause analysis, and documentation.

  • Support the development, execution, and effectiveness verification of CAPAs.

  • Review, revise, and approve controlled documents (SOPs, protocols, reports, forms) in accordance with document control procedures.

  • Apply Quality Engineering principles and Six Sigma / Lean tools to design, evaluate, and implement system or process improvements.

  • Develop, implement, and maintain Sampling Plans based on risk and statistical rationale.

  • Support and execute Change Control activities, including impact assessments and cross-functional coordination.

  • Create, review, and maintain pFMEA documentation to identify, assess, and mitigate process risks.

  • Ensure compliance with GMP, ISO, and applicable regulatory requirements.

Education

  • Bachelor’s degree in Engineering or Sciences.

  • 3–5 years of relevant experience in a regulated industry.

Requirements / Skills

  • Required experience in the Medical Device or Pharmaceutical industry.

  • Strong knowledge and practical experience with GMP and ISO standards.

  • Strong computer skills, including proficiency with MS Office applications (Word, Excel, Outlook) and MS Project Management tools.

  • Solid knowledge of statistics, problem-solving methodologies, and Lean tools.

  • Ability to work effectively in a team-based environment.

  • Demonstrated ability to be a team player, self-starter, persistent, tactful, and persuasive.

  • Strong organizational skills, attention to detail, analytical thinking, and accuracy.

  • Effective verbal and written communication skills, including technical writing and presentations.

  • Ability to work with minimal or no supervision.

  • Fully bilingual in English and Spanish.
     

Ultimate Solutions Corp. is an Equal Opportunity Employer.