Pharma Analytical Development Scientist II

Yoh Services LLC

Corona (CA)

On-site

USD 65,000 - 75,000

Full time

7 days ago
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Benefits offered by this job

Medical, Prescription, Dental & Vision
Health Savings Account (HSA)
Life & Disability Insurance
401K Retirement Savings Plan
Direct Deposit & weekly epayroll
Referral Bonus Programs
Certification and training

Job summary

Yoh, a Day & Zimmermann company, is seeking a Scientist II, Analytics - Product Development for our pharmaceutical client in Corona, CA. You will provide analytical support for product development programs and help advance the development and approval of generic drug products for U.S.

and international markets. This role involves analytical testing with HPLC, GC, UV-Vis, FTIR and Karl Fischer, method development and validation, data management, and collaboration with internal teams, CROs and

Qualifications

  • Bachelor's degree in a science-related field required; advanced degree preferred.
  • 3–6 years of relevant professional experience; 1 year in pharmaceutical R&D preferred.
  • Strong knowledge of analytical chemistry principles and techniques; GMP/GDP familiarity.

Responsibilities

  • Perform analytical testing of raw materials, in-process, finished products, and stability samples.
  • Develop, validate, verify and transfer analytical methods (HPLC, GC, etc.).
  • Document testing per GDP and regulatory requirements; manage data and reports.
  • Collaborate with CROs/CMOs to meet timelines and communicate results.
  • Maintain laboratory equipment, quality systems, and compliance programs.

Skills

Analytical chemistry
English communication
Team collaboration

Education

Bachelor's degree in science
Advanced degree preferred

Tools

HPLC
GC
UV-Vis
FTIR
Karl Fischer
Wet chemistry
Chromatography
Spectrometry

Job description

Yoh, a Day & Zimmermann company, is seeking a Scientist II, Analytics - Product Development for our pharmaceutical client in Corona, CA. You will provide analytical support for product development programs and help advance the development and approval of generic drug products for U.S.

and international markets. This role involves analytical testing with HPLC, GC, UV-Vis, FTIR and Karl Fischer, method development and validation, data management, and collaboration with internal teams, CROs and

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