Plan and execute all analytical related activities in a manner to ensure compliance to the DRAP & RB GLP requirements.
o Raw, FG, WIP materials testing and release on time. Provide status labels accordingly.
o Micro testing of Pharma.
o Understand theory behind analytical techniques & methods.
o Perform standard sample trend analysis & analysis of new source samples
o Support in audit management
o Preparation and update of documents
o Manage and keep all analytical records, data logging, log books and files as per GLP.
o Maintain records clearly identified, labelled, clean and easily accessible.
o Keep up-to-date equipments, test kits, glassware’s, Reagents, chemicals, standards available, labelled and relevant records maintained.
o Perform and maintain record of Equipment Calibration/ functionality tests/Standardization and maintain records.
o Follow all related SOPs while performing any testing activities within the lab.
o Testing should be done as per approved procedures & training provided within the agreed lead time.
o Maintain raw data and all testing results /report.
o Maintain good housekeeping of the lab.
o All responsibilities and authorities shall be hold by QC Executive as deputy to QC Coordinator in his/her absence.
o Ensure strict adherence with Quality Management System(s).
o Any other task assigned by Top Management.
o Ensure compliance & contribute to upkeep and improvement of Health, Safety & Environmental corporate policy/procedures & applicable legal requirements.
Adherence of EHS as per rules and guidelines .
IActivities before execution, work in systematic order and organized the tasks with respect to priorities and timelines Also have creative skills to introduces innovative ideas, take initiatives and efficient in system improvement Proficient knowledge of relevant filed count in my technical skill
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