Quality Assurance Specialist

Evive Health

Irvine, United States
Market-competitive salaries; aggressive bonus stru...
On-site
Bachelor's degree in pharmaceutical sciences or related field
Foundational knowledge of cgmp and fda 21 cfr parts 210/211
Familiarity with hplc, dissolution testing, and karl fischer titration
Evive Health is seeking a detail-oriented Quality Assurance Specialist to join their team in Irvine, California. This junior-level role involves supporting analytical quality processes in a fast-paced pharmaceutical environment, with a focus on compliance with cGMP guidelines

Job Summary

  • This Junior-level role offers an excellent opportunity to build a foundation in pharmaceutical QA within a fast-paced CDMO setting.
  • The position involves reviewing and approving raw material, in-process, and finished product analytical documents under cGMP guidelines.
  • Employees receive full health benefits, paid vacation, sick leave, an aggressive bonus structure, and market-competitive salaries.

Matching Summary

Match Score: 85

Evive Health is seeking a detail-oriented Quality Assurance Specialist to join their team in Irvine, California. This junior-level role involves supporting analytical quality processes in a fast-paced pharmaceutical environment, with a focus on compliance with cGMP guidelines.

Salary

Market-competitive salaries; Aggressive bonus structure; Full health benefits, paid vacation and sick leave

Skills & Requirements

Must-have

  • Bachelor's degree in Pharmaceutical Sciences or related field
  • Foundational knowledge of cGMP and FDA 21 CFR Parts 210/211
  • Familiarity with HPLC, dissolution testing, and Karl Fischer titration
  • Experience reviewing analytical documents and laboratory notebooks
  • Proficiency with Microsoft Office Suite

Nice-to-have

  • Internship or co-op experience in QA/QC environment
  • Strong attention to detail and data integrity mindset
  • Collaboration skills with QC and AD teams
  • Interest in continuous improvement initiatives

Key Requirements

  • Bachelor's degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or related life sciences discipline
  • 0–2 years of experience in pharmaceutical, biotech, or CDMO QA/QC environment
  • Knowledge of ICH guidelines and analytical techniques

Work Rights

Not specified

Tailored Resume

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