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Biopharmaceutical Quality Engineer Jobs (NOW HIRING)

Senior Quality Engineer

Roseville, MN ยท On-site

$92K - $125K/yr

... biopharmaceutical, thermal management (liquid cooling of electronics), medical, industrial, and ... As our next Senior Quality Engineer, you'll be at the forefront of shaping our organization ...

Software Quality Engineer

Santa Clara, CA ยท On-site

$120K - $188K/yr

Join our team as a Software Quality Engineer and play a vital role in developing reliable ... biopharma, diagnostics, or life science tools. * 4+ years of experience working with laboratory ...

Software Quality Engineer

Santa Clara, CA ยท On-site

$120K - $188K/yr

Join our team as a Software Quality Engineer and play a vital role in developing reliable ... biopharma, diagnostics, or life science tools. * 4+ years of experience working with laboratory ...

Quality Engineer

San Lorenzo, PR ยท On-site

$52K - $67K/yr

Quality Engineering Job Category: Scientific/Technology All Job Posting Locations: San Lorenzo, Puerto Rico, United States of America Johnson & Johnson is currently recruiting for a Quality Engineer!

Automation Engineer, Biopharmaceutical The successful candidate will work very closely with the ... Characterize and quantify the quality and efficiency of Xilis' biopharma platform as a whole, and ...

Senior Quality Engineer

Roseville, MN ยท On-site

$92K - $125K/yr

... biopharmaceutical, thermal management (liquid cooling of electronics), medical, industrial, and ... Attend team meetings and provides Quality Engineering input for potential design, process, and ...

New

Senior Device Quality Engineer

Zebulon, GA ยท On-site

$79K - $107K/yr

... engineering, and quality teams. Why You? We seek clear communicators who care about quality and ... Minimum of 8+ years of relevant experience in the pharmaceutical, biopharmaceutical, or related ...

Senior Device Quality Engineer

Zebulon, NC ยท On-site

$75K - $101K/yr

... engineering, and quality teams. Why You? We seek clear communicators who care about quality and ... Minimum of 8+ years of relevant experience in the pharmaceutical, biopharmaceutical, or related ...

Senior Device Quality Engineer

Zebulon, NC ยท On-site

$75K - $101K/yr

... engineering, and quality teams. Why You? We seek clear communicators who care about quality and ... Minimum of 8+ years of relevant experience in the pharmaceutical, biopharmaceutical, or related ...

Showing results 21-40

Biopharmaceutical Quality Engineer information

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$45K

$84K

$119K

How much do biopharmaceutical quality engineer jobs pay per year?

As of Sep 10, 2026, the average yearly pay for biopharmaceutical 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 biopharmaceutical quality engineer do?

A Biopharmaceutical Quality Engineer ensures that products in the biopharmaceutical industry are developed and manufactured in compliance with regulatory standards and quality requirements. They design and implement quality control systems, conduct audits, and analyze production processes to identify areas for improvement. Their work helps guarantee the safety, efficacy, and consistency of medicines and therapeutic products. Quality engineers also collaborate with other departments to solve problems and maintain documentation for regulatory submissions.

What are the key skills and qualifications needed to thrive as a biopharmaceutical quality engineer?

To excel as a Biopharmaceutical Quality Engineer, you need a solid background in engineering or life sciences, experience with quality assurance principles, and familiarity with regulatory standards like GMP and FDA guidelines. Proficiency in quality management systems (QMS), statistical process control software, and root cause analysis tools is typically required. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills in this role. These competencies ensure product safety, regulatory compliance, and the consistent delivery of high-quality biopharmaceutical products.

What are some common challenges faced by biopharmaceutical quality engineers in maintaining compliance with regulatory standards?

Biopharmaceutical Quality Engineers often encounter challenges such as staying updated with evolving regulatory requirements (like FDA, EMA, or ICH guidelines), ensuring documentation accuracy, and managing cross-functional communication between manufacturing, quality assurance, and R&D teams. Strict timelines and the need to quickly address deviations or non-conformances can add pressure to the role. Proactively collaborating with various departments and maintaining a strong understanding of current Good Manufacturing Practices (cGMP) are essential to successfully navigating these challenges.

What is the difference between Biopharmaceutical Quality Engineer vs Quality Control Analyst?

AspectBiopharmaceutical Quality EngineerQuality Control Analyst
CredentialsBachelor's in Life Sciences, Engineering, or related field; certifications like ASQ CQEBachelor's in Chemistry, Biology, or related field; often entry-level
Work EnvironmentManufacturing facilities, labs, quality assurance teamsLaboratories, testing sites, quality control labs
Employer & Industry UsageBiotech and pharmaceutical companies, focusing on product quality and complianceQuality testing labs within pharma companies, contract labs, or manufacturing plants

The Biopharmaceutical Quality Engineer focuses on designing, implementing, and maintaining quality systems to ensure product compliance, while the Quality Control Analyst primarily conducts testing and inspections to verify product quality. Both roles are essential in the pharmaceutical industry but differ in responsibilities and focus areas.

What are popular job titles related to Biopharmaceutical Quality Engineer jobs?

For Biopharmaceutical Quality Engineer jobs, the most frequently searched job titles are:

Infographic showing various Biopharmaceutical Quality Engineer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $84,039 per year, or $40.4 per hour.

Senior Design Quality Engineer

Chaska, MN โ€ข On-site

Lifecore Biomedical
Pharmaceutical and Medicine Manufacturingย โ€ขย 201 - 500 employees

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Senior Design Quality Engineer

Regular Full-Time Chaska, MN, US

It's not what we make, it's what we make possible. And the possibilities at Lifecore are endless!

This full-time position offers incredible benefits, your choice of a 4 ยฝ or 5 day work week, and a company culture focused on development and growth which include promotion opportunities.

We are seeking a Senior Design Quality Engineer to join our MS&T team. In this role, you will provide quality engineering leadership and expertise to technical development programs, new business programs, and customer-facing product development activities. This role partners closely with cross-functional teams and customers to ensure quality is embedded throughout the product development lifecycle through the application of Quality by Design (QbD) principles and Design of Experiments (DOE). You will support the identification of quality, regulatory, and validation requirements early in development to facilitate robust product and process design while effectively meeting customer and business objectives.

In this critical engineering role, you will:

  • Maintain knowledge of best industry practices to provide quality oversight and related initiatives for process development.
  • Ensure validation strategies for clinical and commercial products are developed and executed in compliance with regulatory requirements, supporting robust processes and consistent product quality.
  • Ensure development programs comply with the Quality System and all Design Control requirements.
  • Use quality engineering concepts to monitor, support and critically review process development efforts.
  • Review and approve experimental plans, development processes, equipment/process qualification and controlled documentation.
  • Mentor good experimental technique and statistical/technical data analysis.
  • Ensure data is reviewed and trends are investigated in a manner that ensures robust process quality.
  • Provide guidance in structure of product development process documentation.

This position could be a great fit for you if you have a passion for quality, and the following:

  • BS in Engineering or Life Sciences
  • 5-8 years of quality assurance or quality engineering experience in the medical device or pharmaceutical industry
  • Quality engineering support experience for process improvement or process development.
  • Experience in process/equipment validation.
  • Comprehensive understanding of GMP regulations for medical devices, pharmaceutical products and active pharmaceutical ingredients.
  • In depth understanding of common process development and engineering development activities and proficient in experimental statistical and design of experiments.
  • In depth understanding of design control and regulatory requirements for process design and transfer.
  • In depth understanding of current good manufacturing practices (cGMP) and typical regulatory concerns affecting medical device and/or drug manufacturing.

Starting Salary: $95,000 - $115,00 annually with consideration for relevant skills and experience

Lifecore offers a highly competitive total rewards package, including:

  • Opportunities to learn and grow with a well-respected company
  • Competitive compensation with annual reviews and a company-wide incentive bonus
  • Benefits that start the first of the month after you join Lifecore as a full-time employee:
    • 3 medical insurance plans to fit your needs and budget including an HSA Plan with company contributions.
    • Low cost dental and vision insurance
    • Short term disability, long term disability and life insurance all 100% company paid
    • 3 weeks PTO in the first year (increases to 4 weeks after just 2 years!)
    • 9 paid company holidays plus 2 personal holidays
    • Paid family leave
    • Tuition reimbursement
    • 401k plan with company matching contribution

Meet Lifecore Biomedical, LLC:

Lifecore Biomedical, Inc. (Nasdaq: LFCR ) is a fully integrated contract development and manufacturing organization (CDMO) that offers highly differentiated capabilities in the development, fill and finish of sterile injectable pharmaceutical products in syringes, vials, and cartridges, including complex formulations. As a leading manufacturer of premium, injectable-grade hyaluronic acid, Lifecore brings more than 40 years of expertise as a partner for global and emerging biopharmaceutical and biotechnology companies across multiple therapeutic categories.

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