Analytical Development Analyst

PharmaPath is seeking to hire an Analytical Development Analyst for its R&D activities.

Main duties and 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.