Analytical Reviewer

Contrat à durée indéterminée (CDI), Temps plein · Athens, Attiki, Greece

Our offer
  • Competitive salary.
  • Health Insurance.
  • Pension program.
  • High-level training on GMP and technical aspects of current industry trends and requirements.
  • Stimulating scientific environment that fosters motivation
Your mission
Your mission
Adragos Pharma Athens (member of Adragos Pharma) is an innovative contract development company based in Europe. Our primary focus is to provide high-quality research for the development of generic and generic-plus products. With a team of highly experienced professionals who have worked on numerous molecules, Adragos Pharma Athens is seeking to hire an analytical reviewer for our GMP Analytical department.
 
Responsibilities:
 
  • Undertaking and overseeing the complete review process of analytical results.
  • Generating & reviewing analytical methods.
  • Generate reports and evaluate results obtained from analytical testing.
  • Identify, document and report any analytical issues encountered and participate in out-of-specification and failure investigations and recommend corrective actions.
  • Support the Department in aspects of Quality assurance, control and reporting.
Your profile
  • Possess a Bachelor's degree in Life Sciences, preferably with a specialization in Chemistry.
  • Demonstrate good knowledge and familiarity with ICH guidelines and principles.
  • Have a minimum of two (2) years of professional experience in the field of pharmaceutical analysis.
  • Proficiency in analytical chromatography techniques and troubleshooting.
  • Familiarity with software Empower 3 will be considered a valuable asset.
  • Familiarity with working in a GLP/GMP oriented laboratory.
  • Ability to multitask effectively.
  • Fluent in both written and oral English.
  • Proficient in computer skills, particularly Microsoft Office.
  • An MSc in Chemical or Pharmaceutical Analysis will be considered a valuable asset.
About us
Adragos Pharma is a reliable Contract Development and Manufacturing Organization (CDMO) headquartered in Munich, Germany. We provide comprehensive development and manufacturing services for drug products, including sterile and non-sterile liquids, solids, and semi-solids. Our expertise also covers biologicals, orphan drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply.

With production sites in Germany, France, Greece, Norway, Japan, and Switzerland, we ensure high-quality manufacturing across all stages of the drug development process. 

Founded in 2020, Adragos Pharma has rapidly grown through an ambitious buy & build strategy, supported by FSN Capital. With a team of over 900 professionals, we are expanding our operations across Europe, North America, and Japan to become a global leader in the CDMO sector.

As a key player in the pharmaceutical industry, CDMOs like Adragos produce 25% of all drugs globally, ensuring access to essential medications. With increasing healthcare demands, we continue to innovate and set new standards in drug manufacturing.

You want to be part of our dynamic growth? Then apply now!   
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