QC Analyst - Αναλυτής ποιοτικού ελέγχου φαρμακευτικών προϊόντων

VIOFAR LTD, a pharmaceutical company based in Acharnes - Attica is looking to hire QC ANALYST to staff the Quality Control department in a GLP/GMP environment.

Main duties and Responsibilities

• Prepare high quality technical documents required for analytical purposes
• Implement analytical methods for in process and finished pharmaceutical products
• Perform analysis at raw and packing materials
• Review analytical data and results
• Support the drafting of scientific texts and study reports
• Keep the laboratory documents and logbooks update
• Identify, document and report analytical issues
• Maintain and follow all laboratory systems
• Perform daily calibration of analytical equipment.
• Adhere to safety and housekeeping requirements
• Manage deliverables and ensure that necessary supplies such as standards, reagents, columns, impurities are available on time for projects

Requirements - The ideal candidate should have:

• BSc in Chemistry or Biochemistry
• At least 1 year of experience in the Pharmaceutical Industry within the field of pharmaceutical analysis, Quality Control, R&D analytical
• Experience in a GLP / GMP oriented laboratory
• Excellent communication in English language (writing & speaking)
• Knowledge of cGMP, USP/NF, ICH, DEA, EU and FDA guidelines and regulations will be considered an asset
• Strong problem-solving, troubleshooting skills
• Demonstrated ability to work on multiple projects and meet timelines
• Ability to work in SHIFTS

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