Lonza

Manufacturing Specialist, Quality Assurance (Night Shift)(Night Shift)

Job ID: R75465
Location
Bend, OR
Hours/week
40 hrs/week
Payrate range
Unknown

The actual location of this job is in Bend, Oregon. Relocation assistance is available for eligible candidates and their families, if needed.

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.
 

Note:  Schedule will be 4 ten hour shifts Sunday through Wednesday nights (4pm-3am including 1 hour lunch).

What you will get:

  • An agile career and dynamic working culture.

  • An inclusive and ethical workplace.

  • Compensation programs that recognize high performance.

  • Medical, dental and vision insurance.

  • The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits.

What you will do:

  • Perform Area Clearance events.

  • Status labeling of product, such as QA Hold/Rejected.

  • Review Production Records for accuracy and compliance.

  • Support implementation and continuous improvement of Quality Systems.

  • Oversee product compliance during product manufacturing.

  • Recommend compliance enhancements to the Manufacturing area.

  • Assist with manufacturing investigations, root cause analysis, and corrective and preventive actions, as needed.

  • Assure that the manufacturing of product is performed according to SOPs and current GMPs.

  • Communicate and escalate potential non-compliant and adverse events to QA Management.

What we are looking for:

  • Experience in pharmaceutical/biotechnology or related industry.

  • Independent and flexible worker that can readily adapt to changing priorities in a fast-paced cutting-edge environment.

  • Knowledge of QA and FDA regulations for clinical trials materials.

  • Experience with operational deviations and global investigations participation strongly preferred.

  • Demonstrated attention to detail and excellent oral and written communication skills.

  • Must be available on weekends or on-call occasionally as needed.

  • Requires consistent, in-person attendance.

  • Must be able to work while wearing personal protective equipment as needed.

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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