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Quality Control Senior Analyst

Grünenthal Group · Quito

Onsite Senior 🇬🇧 English
HPLC GMP GLP

Job description

About the role

Join an international, collaborative team dedicated to ensuring the highest quality of pharmaceutical products. As a Quality Control Senior Analyst you will directly influence product reliability and patient safety by applying rigorous analytical methods and continuous improvement practices.

Key responsibilities

  • Perform release testing of semi‑finished products, guaranteeing compliance with established quality standards.
  • Operate laboratory equipment, notably High‑Performance Liquid Chromatography (HPLC), with precision and accountability.
  • Interpret analytical results, generate timely reports, and meet departmental KPIs.
  • Drive continuous improvement initiatives and adapt to evolving processes, guidelines, and innovations.
  • Apply Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) in all laboratory activities.

Required profile

  • Degree in Pharmaceutical Chemistry, Chemistry, Chemical Engineering or a related field.
  • Minimum 2 years of experience in a pharmaceutical environment.
  • Intermediate proficiency in English to understand technical documentation.
  • Strong organizational mindset, proactive attitude, and a focus on teamwork and compliance.
  • Availability to work in shifts.

Required skills

  • High‑Performance Liquid Chromatography (HPLC)
  • Good Manufacturing Practices (GMP)
  • Good Laboratory Practices (GLP)

Questions fréquentes

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Published 2 months ago

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Grünenthal Group

Quito