Analytical Development Analyst

2 days ago

Athens, Attica, Greece PharmaPath Full time €40,000 - €60,000 per year
PharmaPath, a Greek pharmaceutical company with a rich history and significant legacy in the pharmaceutical field of generic medicines, is seeking a dedicated and skilled Analytical Development Analyst to join our dynamic team Main duties & key responsibilities:
  • Performs daily analysis according to the relevant analytical methods and daily analysis program for lab-scale batches, pilot batches, stability studies, APIs and excipients
  • Performs sampling for APIs and excipients according to the relevant SOPs if necessary
  • Executes Method Development, Method Validation and Method Transfer protocols
  • Performs daily instrument calibrations according to the relevant procedures (balances, pH meters, Karl Fischer titer determination etc)
  • Records all data and results in specified forms (paper and electronic) with accuracy and responsibility
  • Performs integration of chromatograms according to the relevant procedures, calculates and evaluates the daily analytical results
  • Conducts data review to ensure completeness and accuracy of records and notifies the Senior Manager or Senior Analyst in case of OOS/OOT results and / or instrument, system suitability failure
  • Follows the laboratory safety rules
  • Cleans the laboratory equipment and laboratory areas according to schedule
  • Organizes and stores all chemicals substances, solvents, standards, samples and columns according to internal procedures instructions. Disposes all expired solvents, standards, analyzed samples according to the internal procedures
  • Places samples in the stability chambers. Removes and disposes stability samples according to the relevant schedule
  • Assists in maintenance and troubleshooting of instruments
  • Assists in ordering laboratory supplies
Requirements:
  • Bachelor Degree in Chemistry, Pharmacy or any other relevant field
  • Minimum 1 year of experience in R&D pharmaceutical laboratory
  • Working experience in pharmaceutical analytical techniques such as HPLC, GC, UV-Vis and Empower 3 software
  • Previous experience with Method Development, Method Validation and Method Transfer activities
  • Comprehensive understanding of Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Safety regulations and Quality Assurance Systems
  • Strong problem-solving attitude & results orientation
  • Attention to detail with focus on deliverables, quality and project timelines
  • Fluent in Greek & English
Benefits:
  • Competitive remuneration package, including benefits
  • Ability to become part of one of the most dynamic and prospective teams in the Pharmaceutical industry in Greece
  • Continuous opportunities in advancing personal and career goals

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