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QC Analyst

Job in Vacaville, Solano County, California, 95688, USA
Listing for: Lonza
Full Time position
Listed on 2026-06-21
Job specializations:
  • Quality Assurance - QA/QC
    Quality Technician/ Inspector, QA Specialist / Manager, Quality Control / Manager
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Location: Vacaville, CA. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

United States, Vacaville (California).

What You Will Get

Full‑time base annual salary: $56,250 to $93,750. Benefits include:

  • Performance‑related bonus
  • Medical, dental and vision insurance
  • 401(k) matching plan
  • Life insurance, and short‑term and long‑term disability insurance
  • Employee assistance programs
  • Paid Time Off
What You Will Do
  • Perform a broad variety of basic lab activities and prepare basic and complex reagents to consistently support laboratory operations and testing workflows.
  • Review GMP documentation and maintain a continuous state of inspection readiness to ensure strict regulatory compliance.
  • Perform routine lab maintenance and equipment qualification/maintenance to guarantee system reliability and data accuracy.
  • Identify and recommend solutions to potential procedural and process system gaps, actively participating in teamwork for process improvements.
  • Recognize deviations from accepted practices while working on semi‑routine assignments and problems of limited scope.
  • Improve laboratory inventory processes and use laboratory computer systems and Microsoft Suites to enable efficient operations.
  • Coordinate with testing analysts and manage competing priorities with instruction to support broader team operational activities.
What We Are Looking For
  • Degree/Diploma in a relevant Science field, or equivalent experience.
  • Relevant work experience, with a strong preference for GMP/Lab experience in a biotech or medically related field.
  • Ability to work comfortably and effectively in a production floor setting.
  • Adaptability to receiving detailed instructions and performing assigned duties according to specified procedures.
About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.

Reference: R77046

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