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Batch Records Engineer Jobs (NOW HIRING)

Aquestive Therapeutics

Process Engineer

Portage, IN · On-site

Establishes the product manufacturing control strategy and implements into Batch Records. * Finalizes the QTPP (Quality Target Product Profile). * Represents Engineering Subject Matter Expert (SME ...

Aquestive Therapeutics

Process Engineer

Portage, IN · On-site

Establishes the product manufacturing control strategy and implements into Batch Records. * Finalizes the QTPP (Quality Target Product Profile). * Represents Engineering Subject Matter Expert (SME ...

Pyramid Laboratories Inc

QA Specialist

Costa Mesa, CA · On-site

$65K - $75K/yr

Batch Record Review * Independently review executed batch records and associated documents (testing ... Bachelor's degree in Biology, Chemistry, Pharmaceutical Sciences, Engineering, or related field ...

Pyramid Laboratories Inc

QA Specialist

Costa Mesa, CA · On-site

$65K - $75K/yr

Batch Record Review * Independently review executed batch records and associated documents (testing ... Bachelor's degree in Biology, Chemistry, Pharmaceutical Sciences, Engineering, or related field ...

Terrestrial Bio

$72K - $91K/yr

Author, edit, and review batch records, SOPs, and work instructions * Communicate progress, issues, and results to key stakeholders WHAT YOU BRING * Engineer I - BS in Chemical Engineering ...

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Batch Records Engineer information

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How much do batch records engineer jobs pay per year?

As of Sep 10, 2026, the average yearly pay for batch records engineer in the United States is $69,362.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,500.00 and $78,500.00 per year, depending on experience, location, and employer.

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For Batch Records Engineer jobs, the most frequently searched job titles are:

Infographic showing various Batch Records Engineer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $69,362 per year, or $33.3 per hour.

Batch Release Specialist, Quality Assurance Operations

Houston, TX • On-site

Lonza
Biotechnology Research and Development • 10K+ employees
Learn more about Lonzaexternal

Full-time

Re-posted 16 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

Job description

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

Key responsibilities:

  • Disposition of batches manufactured at the LHI site, including maintaining a batch release tracking system.

  • Collaborating with other teams to ensure all necessary tasks for batch disposition are finished, including performed batch records, deviations, change controls, and Environmental Monitoring reports.

  • Mentoring junior staff members in helping to address feedback on batch records and test record forms.

  • Collaborating with the Project Management and QA leadership teams to implement changes to the batch release process, improving compliance, effectiveness, and efficiency.

  • Identifying and implementing improvements in the Quality Systems to boost compliance and efficiency.

  • Maintaining quality systems and cGMP compliance by ensuring team adherence to processes, procedures, and instructions.

  • Promoting and ensuring job safety, attending required health and safety training, and reporting any actual or potential accidents and injuries promptly.

Key requirements:

  • Bachelor's degree in life sciences (biotechnology, biochemistry, biology, chemistry, engineering) or related field.

  • Proven track record (7-10 years) in batch disposition activities within a cGMP environment.

  • Direct GMP experience within the pharmaceutical industry.

  • Proficiency in Root Cause Analysis Tools, Risk Management, Technical Writing, Microsoft Office applications, TrackWise, DMS, SAP, and LIMS systems preferred.

  • Strong contributor who prioritizes safety, quality, and timelines.

  • Knowledge of GMP compliance, including 21CFR210, 211, 820, and the PICS Guide to Good Manufacturing Practices, ICH Q7, 13485, and Part 11 compliance preferred.

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US

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