Davipharm

Job description:

• Perform according to the assigned tasks from team leader.
• Preparation of general-purpose reagents, performing standard solutions, indicators, buffers, etc.
• Checking room and equipment temperature, humidity in physicochemical Laboratory and record results.
• Supervising the assigned control and measurement equipment.
• Conducting and documenting testing in the scope of physicochemical analysis with all methods used in the laboratory.
• Report to the person responsible about of the status quantity, expiry, quality of chemical/standards.
• Participation in OOX investigation, open deviation.
• Developing and giving opinions on the implementation of the quality system in the Quality Control Laboratory (instructions for equipment).
• Cooperate and support other sub-teams as assigned.
• Training new laboratory staff.
• Training employees the related procedure, contents upon request.
• Preparing, checking analytical reports and Certificates of Analysis.
• Performing the transfer of analytical methods transferred from another laboratory. Participation in the implementation of new products in analytical subjects.
• Prepare the protocol, report, perform validation analytical method, cleaning validation, dissolution profile, recomendation.
• Solving everyday problems related to testing of raw material, in-process control, finished product, stability studies.
• Creating reports, summaries, summaries of the resulting investigations along with the interpretation of the results and recommendations received.
• Perform the calibration of laboratory glassware.
• Participation in investigation of deviation.
• Participate in URS drafting and validation of simple spreadsheet.
• Participate in the CAPA, change control implementation related to QC.
• Guaranteed implementation the data integrity in QC department.
• Opex management and budget controlling.
• Report the Kaizen ideas to leader/ manager and take part in to prepare those potential ideas.
• Receiving samples – Registering samples – Distributing samples – Archiving samples according to the approved procedure

Job requirement:

• Vocational school in pharmaceutical/ chemical/ biological field, at least.
• Have 1 to 3 years working in laboratory.
• Have knowledge of Good Laboratory practice (GLP) and Good manufacturing practice (GMP) rules.
• Operation skill on analytical equipment (HPLC, UV-Vis, IR, GC,…)
• Ability to work under pressure high and intensive deadlines.
• MS Office: Microsoft Excel, Word
• Good communication skill and working with group.
• Have ability to prepare documentation according to the internal procedures.

Please contact our Recruiter or apply via email recruitment@davipharm.info