Analista De Control De Calidad

Abbott

Lima, Peru
3+ years experience in analytical method development
Knowledge of gmp and glp regulations
Proficiency with hplc, gc, uv, ir, and atomic absorption
This position is located at the Lince headquarters within Abbott's Established Pharma division, focusing on a diverse portfolio of generic medications

Job Summary

  • This position is located at the Lince headquarters within Abbott's Established Pharma division, focusing on a diverse portfolio of generic medications.
  • The successful candidate will be responsible for developing analytical methodologies for commercial products required for regulatory filings and managing laboratory investigations.
  • Abbott offers a supportive environment where employees can grow, learn, and contribute to innovative healthcare solutions while adhering to strict quality standards.

Matching Summary

This position is located at the Lince headquarters within Abbott's Established Pharma division, focusing on a diverse portfolio of generic medications.

Skills & Requirements

Must-have

  • 3+ years experience in analytical method development
  • Knowledge of GMP and GLP regulations
  • Proficiency with HPLC, GC, UV, IR, and Atomic Absorption

Nice-to-have

  • Intermediate Microsoft Office skills
  • Experience with regulatory submission support
  • Ability to work in a team environment

Key Requirements

  • Licensed Pharmacist-Chemist (Químico Farmacéutico Titulado)
  • Minimum 3 years experience in Pharmaceutical Industry
  • Experience in Method Development, Validation, and Transfer

Work Rights

Not specified

Tailored Resume

Cover Letter