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Pharmaceutical Quality Engineer Jobs (NOW HIRING)

McKesson

Sr Associate Quality Engineer

Louisville, KY · On-site

$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

Integrated Resources INC

Quality Engineer

Franklin Lakes, NJ · On-site

$73K - $94K/yr

Qualifications BS degree in Quality or Life Sciences, Engineering (Biology, Chemistry, Microbiology,) and a minimum of 5-6 years of experience in Pharmaceutical/Biotechnology Industry required ...

ALOIS LLC

Quality Engineer

El Paso, TX · 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 ...

NEPHRON SC, LLC

QUALITY ENGINEER

West Columbia, SC · On-site

$65K - $84K/yr

The Quality Engineer supports aseptic manufacturing operations by executing quality system ... in pharmaceutical manufacturing or a related industry, with a strong understanding of ...

Healthcare

Quality Engineer

Monrovia, CA · On-site

$106K - $145K/yr

Bachelor's Degree or higher in engineering or science from an accredited institution and three (3) years of quality engineering experience in a medical device and/or pharmaceutical company in a ...

Intellectt INC

Quality Engineer

Chicago, IL · On-site

$74K - $95K/yr

Quality Engineer Location: Chicago, IL or Northfield, IL Duration: Longterm Job Summary The Quality ... quality systems roles within medical devices, pharmaceuticals, or regulated healthcare ...

Solventum

Quality Engineer

Monrovia, CA · On-site

$106K - $145K/yr

Bachelor's Degree or higher in engineering or science from an accredited institution and three (3) years of quality engineering experience in a medical device and/or pharmaceutical company in a ...

Comar Engineering Services

Quality Engineer

Buena, NJ · 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 ...

AppleOne

Quality Engineer

Caguas, PR

$26/hr

This role is ideal for an engineering professional with experience in quality, compliance, validation, and continuous improvement within medical device or pharmaceutical manufacturing. The Quality ...

Ecolab

Quality Engineer

Philadelphia, PA · On-site

$74K - $112K/yr

... Quality Engineer at our manufacturing site in Philadelphia, PA ... We manufacture products which help our customers around the globe, mainly in pharmaceutical and ...

Ecolab

Quality Engineer

Philadelphia, PA

$74K - $112K/yr

... Quality Engineer at our manufacturing site in Philadelphia, PA ... We manufacture products which help our customers around the globe, mainly in pharmaceutical and ...

Ultimate Solutions

$67K - $87K/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 ...

Recruits Lab

Quality Engineer

Phillipsburg, NJ

$36.06 - $43.27/hr

Quality Engineer (Contract) - GMP / ISO Environment Location: Phillipsburg, NJ (100% Onsite ... Experience in pharmaceutical, biotechnology, or chemical manufacturing environments * Strong ...

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Pharmaceutical Quality Engineer information

See salary details

$45K

$84K

$119K

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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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 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.
Sr Associate Quality Engineer

Sr Associate Quality Engineer

McKesson

Shepherdsville, KY • On-site

$65K - $109K/yr

Full-time

Posted 23 days ago

McKesson rating

7.8

Company rating: 7.8 out of 10

Based on 202 frontline employees who took The Breakroom Quiz

41st of 71 rated pharmaceutical

Job description

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve - we care.

What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow's health today, we want to hear from you.

The Senior Associate Quality Engineer is responsible for advanced quality oversight across daily operations, incident management, investigations, and client-facing quality activities. This position partners with Operations, Account Management, and internal/external customers to act as a quality liaison to drive risk-based decision making, identifies emerging quality risks, and contributes to continuous improvement initiatives to strengthen compliance and process efficiency.

Key Responsibilities

  • Responsible for the oversight of the Corrective Action/Preventive Action ("CAPA") program for their area of responsibility including but not limited to review all non-conformances to ensure they are documented, review all corrective/preventive actions for completeness, and execute effectiveness checks when required.

  • Assist with Non-conformance Investigations assigned to Quality Assurance, as needed. Responsible for ensuring timely closure of CAPA records.

  • Responsible for generating status reports from applicable QMS applications, analyzing data to identify potential trends and areas for improvement, and maintaining related company measurements.

  • Responsible for repackaging and relabeling projects in support of client requests, as Project Leader. Including, but not limited to, communication with client and Program Manager regarding project details, pricing proposals for project, creation of the project protocol, inspection of the project as required by project protocol, and filing any necessary paperwork with client, Program Manager, and/or regulators.

  • Manages all special client project requests, client complaint memos, and other relevant client memos.

  • Serves as a back-up for the Associate Quality Engineer to perform the inspection and release process for incoming and returned product including but not limited to: downloading and review of temperature device data, communicating results to clients, obtaining proper client approval, electronic storage of inspection records, and product retains.

  • Assists as needed with Client and Regulatory activities, Quality-related training, validation of storage areas/systems/equipment where required, and other duties and responsibilities as assigned by manager.

Shift:

11:00AM - 7:30pmTHIS ROLE REQUIRES YOU TO BE ON SITE 5 DAYS A WEEK.

Minimum Job Qualifications:

Degree or equivalent and typically requires 2+ years of relevant experience.

Critical Skills:

  • 3-5 years in a pharmaceutical quality/regulatory environment, preferred

  • Quality Management System and/or Document control management experience, preferred.

  • Knowledge of pharmaceutical regulations, including FDA requirements, preferred.

Preferred Skills:

  • Ability to express ideas clearly both in written and oral communications.

  • Ability to enter data accurately.

  • Ability to handle multiple tasks well.

  • Detail-oriented individual with thorough knowledge of word processing, database, and spreadsheet programs (preferably MS Office).

  • Must possess the ability to work with internal departments to accomplish objectives and meet established deadlines.

  • Must be personable, self-starter, possess a good attitude, and enjoy external and internal contact on the phone and in person with supervisors, co-workers, customers, and potential clients.

We are proud to offer a competitive compensation package at McKesson as part of our Total Rewards. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. The pay range shown below is aligned with McKesson's pay philosophy, and pay will always be compliant with any applicable regulations. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered. For more information regarding benefits at McKesson, pleaseclick here.

Our Base Pay Range for this position

$65,600 - $109,300

McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson's (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:
McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.


McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.

McKesson job postings are posted on our career site: careers.mckesson.com.

McKesson is an Equal Opportunity Employer

McKesson provides equal employment opportunities to applicants and employees, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other legally protected category. For additional information on McKesson's full Equal Employment Opportunity policies, visit our Equal Employment Opportunity page.

McKesson is committed to being an Equal Employment Opportunity Employer and offers opportunities to all job seekers including job seekers with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to (United States) Disability_Accommodation@McKesson.com or (Canada) Accessibility@mckesson.ca. Resumes or CVs submitted to this email box will not be accepted.

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