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Quality Control Associate

Lonza

Vacaville, CAOnsitePosted 2 days ago$78,000 - $130,000/year
Full TimeSenior LevelQuality (QA / QC)CDMO
Original posting ↗

Summary

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.

Job description

The Quality Control Associate performs specialized technical tasks as assigned within the Quality Control organization such as operational roles (i.e. laboratory testing) and/or support roles (i.e. deviation management). Executes job duties in alignment with Quality Control policies, procedures, specification and testing methods consistent with cGMP, EHS requirements, applicable regulations, and Lonza standards, policies, plans, objectives, and procedures. Conducts work to meet customer commitments.

What you will do:

  • Perform specialized technical tasks as assigned within the Quality Control organization such as operational roles (i.e. laboratory testing) and/or support roles (i.e. deviation management).
  • Execute job duties in alignment with Quality Control policies, procedures, specification and testing methods consistent with cGMP, EHS requirements, applicable regulations, and Lonza standards, policies, plans, objectives, and procedures.
  • Conduct work to meet customer commitments.

What we look for:

  • Bachelor Degree in Science or relevant Scientific Discipline
  • 5-10 years of experience in Quality Control, or equivalent professional experience, with experience in cell based assays, ELISA, or other potency methods
  • Effective communication at all levels
  • Ability to secure relevant information and identify key issues and relationships from a base of information
  • Adapt to changing conditions
  • Ability to prioritize deliverables

Requirements

  • Bachelor Degree in Science or relevant Scientific Discipline
  • 5-10 years of experience in Quality Control, or equivalent professional experience
  • Experience in cell based assays, ELISA, or other potency methods
  • Effective communication at all levels
  • Ability to secure relevant information and identify key issues and relationships from a base of information
  • Adapt to changing conditions
  • Ability to prioritize deliverables

Benefits

  • Performance-related bonus
  • Medical, Dental & Vision
  • 401(k) Matching
  • Life Insurance
  • Short & Long-Term Disability
  • Employee Assistance Programs
  • Paid Time Off

Company overview

Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.

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