GMP Quality Control Scientist – Analytical Lab

Bachem Holding AG

California, Northern (MO, KY)

Hybrid

USD 60,000 - 120,000

Full time

14 days+
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Benefits offered by this job

Medical/Dental/Vision coverage
401(k) with employer contribution
Paid vacation and sick days

Job summary

Bachem Americas is seeking a Quality Control Scientist to lead day-to-day QC operations in a GMP manufacturing environment. You will coordinate with QC leadership, perform raw material, in-process, and final product testing, and ensure documentation and control of QC processes across multiple analytical platforms.

The role requires proficiency with HPLC/UPLC, GC, UV-Vis spectroscopy, and Mass Spectrometry, along with strong data review and GMP documentation skills.

Qualifications

  • Experience with analytical techniques and instrumentation used for GMP QC
  • Ability to write and revise specifications, SOPs and GMP documentation
  • Knowledge of cGMP requirements and QC procedures
  • Strong documentation and data review skills
  • Ability to train and supervise QC staff and maintain equipment GMP compliance

Responsibilities

  • Maintain daily QC operations coordinating with QC Director/Supervisor
  • Test and release raw materials, in-process and final products
  • Verify QC equipment and GMP compliance
  • Write and revise QC documents, SOPs and STPs
  • Perform analytical testing (HPLC/UPLC, GC, UV, Mass Spec) and review data
  • Maintain cGMP quality, training, and documentation
  • Investigate deviations and perform validations to support QC
  • Ensure safe handling of chemicals and compliance with safety guidelines

Skills

HPLC/UPLC
GC
UV-Spectrophotometer
Mass Spectrometry
Analytical data review
Documentation

Education

Bachelor’s degree in chemistry or related field
Master’s degree in chemistry or related field (preferred)

Job description

Bachem Americas is seeking a Quality Control Scientist to lead day-to-day QC operations in a GMP manufacturing environment. You will coordinate with QC leadership, perform raw material, in-process, and final product testing, and ensure documentation and control of QC processes across multiple analytical platforms.

The role requires proficiency with HPLC/UPLC, GC, UV-Vis spectroscopy, and Mass Spectrometry, along with strong data review and GMP documentation skills.

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