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, 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)