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

Απαραίτητα Προσόντα: Requirements - The ideal candidate should have: BSc in Chemistry, Biochemistry, Pharmacy etc. At least 3 year of experience in the Pharmaceutical Industry as an HPLC USER (Agilent, Shimadzhu, Waters) : please give details in your CV 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 (6am-2pm, 2pm-10pm) Παροχές: