Candidate should be capable of operating Analytical instruments such as HPLC, GC,Dissolution Appratus, UV, IR, KF etc. should be aware and capable of Qualitative, Quantitative, Sample, Wet, Routine analysis of drug substances, intermediates, finished products, raw materials etc.
Supports to the Laboratory functions to handle Investigations, Deviation Management, Specifications ,test methods, method validations equipment qualifications ,internal audits and escalations if any.
Responsible for post approval submissions to Europe, Australia, New Zealand and Canada market. To provide Regulatory inputs during inspections by Regulatory authorities and Customer as and when required.
Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant note books. They are to follow instructions from the supervisor and work in a group to accomplish the tasks in a timely and efficient manner.