QC Associate Scientist

Astrix Inc

$75K — $90K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in chemistry or related field
  • Minimum of 3 years' hands-on experience performing HPLC and GC analysis within GMP pharmaceutical manufacturing
  • Demonstrated experience in analytical method transfers
  • Strong working knowledge of GLP/GMP standards, quality control procedures, and laboratory documentation practices

Responsibilities

  • Perform routine HPLC and GC analysis to support API method transfers, including compliance with GMP standards
  • May conduct other analytical testing such as FTIR, KF, NMR
  • Prepare protocols and reports to support GMP method transfers
  • Conduct release testing for raw materials, intermediates, and APIs
  • Investigate out-of-specification (OOS) results and document findings
  • Generate accurate data timely to meet project deadlines
  • Review analytical data for accuracy and Good Documentation Practices (GDP) compliance

Benefits

  • PTO
  • Health/vision/dental insurance
  • HSA
  • 401(k) with match
  • Holiday pay
Full Job Description
Pay Rate Low: 75000 | Pay Rate High: 90000
We're hiring an Associate Scientist with analytical experience to join a global leader in the development and production of active pharmaceutical ingredients (APIs) for CDMO partners and generic drugs. This is a great opportunity to work with an industry leader that focuses on their expertise and competence in all of the companies processes!

Schedule: M-F 8a-5p

Location: Lake County, OH

***Benefits include***
PTO, health/vision/dental insurance, HSA, 401(k) with match, and holiday pay!

Responsibilities:
  • Perform routine HPLC and GC analysis to support API method transfers, including data generation, interpretation, and documentation in compliance with GMP standards
  • May perform other analytical testing (e.g., FTIR, KF, NMR)
  • Support GMP method transfers, including protocol/report preparation
  • Conduct release testing for raw materials, intermediates, and APIs
  • Investigate out-of-specification (OOS) results and document findings
  • Ensure timely and compliant data generation to meet project timelines
  • Review analytical data for accuracy and GDP compliance

Qualifications:
  • Bachelor's degree in chemistry or related field
  • Minimum of 3 years' hands-on experience performing HPLC and GC analysis within GMP pharmaceutical manufacturing
  • Demonstrated experience in analytical method transfers
  • Strong working knowledge of GLP/GMP standards, quality control procedures, and laboratory documentation practices

***This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!***

INDBH
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