 To planning and execution of in process and finished product samples analysis. Planning and execution of the stability sample analysis within defined time frame as per monthly stability sample withdrawal schedule. Preparation of shift schedule and allotment of effective responsibilities/works to the subordinates. Try to minimize the laboratory error by encouraging the subordinate’s works. One to one Interaction with the subordinates for their troubles and resolution. To maintain the effective communication with the production, IPQA, R&D and Project management department. Actively Involvement in the laboratory incidents, Out of Trend and Out Of Specifications investigation in all laboratory areas. Troubleshooting of Sophisticated Instruments in Laboratory. Maintained all laboratory records and documentation as per GMP. Involvement in SOP preparation as per regulatory requirement and regulatory updation. To maintain and planning the yearly and monthly instruments calibration and Preventive maintenance schedule. Actively involvement in daily and periodic instruments calibration, maintain calibration records.  Interact with Service Engineer regarding instruments Preventive maintenance schedule, instrument breakdown and other instruments related queries. Involvement in Deviation/Change control procedure with effective CAPA. Maintaining of and carrying out IQ, OQ & PQ of instruments in the lab. Support any new initiative and responsibilities as allocated.

 To participate in regulatory and customer audits for laboratory and stability areas. Reviewing and approving finish product protocols, reports, finished specification and in-process specification. Reviewing of SOPs, Specifications and test procedure(s), Technology transfer protocols/reports and all other documents prepared under laboratory area. Reviewing daily, weekly and monthly instruments calibration records and ensures that effective systems are used in maintaining for calibration of Instrument.  Actively involved in CRAMS projects. Ensure that all technical requirements and procedures for the technology transfer of analytical test methods from customer are accessible in laboratory and corresponds to the customer for any requirements.  Interact with Contact giver regarding any analytical issues during technology transfer activity and resolved it by mutual understanding with contract giver. To maintain the effective communication system between Quality control, Production, QA department, Project managements, Marketing and RA. Work with the Regulatory Affairs department to ensure analytical test methods and validation activities are prioritized, planed and delivered in a timely manner in order to meet given regulatory filing strategy. To organize stability program and to conduct according to the pre determined schedule / protocol. Interact with service engineers of stability chambers for servicing, calibration and other maintenance related work. Make sure that the stability data available to support retest or expiry dates and storage condition for finished product and/or intermediates as appropriate. To make sure that the laboratory incidents and Out Of Specifications are investigated and resolved in all laboratory areas. Allotment of effective responsibilities and work to the subordinates. Support any new initiative and responsibilities as allocated.

 Actively Involvement in Report reviewing and SOP preparation. Actively involvement in OOS investigation and laboratory Incidence. Involvement in Deviation/Change control procedure. Maintained all laboratory records and documentation as per GMP. Maintaining of and carrying out IQ, OQ & PQ of instruments in the lab. Involved in maintenance and calibration of laboratory equipments. Involvement in Analytical method transfer.  Routine analysis of Tablet, Capsules, Liquid oral and Sami-solids dosages form. Experienced in using HPLC, GC, Dissolution studies, Karl Fischer apparatus and Wet Chemistry experiments. Active involvement in stability sample charging and discharging as per customer/in house protocol, also maintain temperature recording of stability chamber. Troubleshooting of Sophisticated Instruments in Laboratory Using a range of bench tests and instrumental techniques to provide Quality Control on incoming samples to ensure compliance with in-house specifications, Customer Specification and related Pharmacopeia methods.  Knowledge of GLP, cGMP, Laboratory health and safety requirements and COSHH regulations. Involved in preparation and maintenance of stock solutions and also responsible for maintaining cleanliness according to GMP/GLP standards. Knowledge of LIMS (OASIS) for pharmaceutical sample data recording computerized system.  Work distribution with the help of team leader. Any other duties deemed necessary in the department.

 Using a range of bench tests and instrumental techniques to provide Quality Control on incoming materials to ensure compliance with both in-house specifications and EC/UK regulations  Maintenance of all laboratory equipment to ensure it is in good working order and calibrated to ISO 9000 and CLAS standards. Quality Control on outgoing products ensuring they meet specified standards Maintenance of all laboratory analysis records, inputting them to computer and manipulation of this data where necessary to generate information. Archiving samples for customer reference; making up accurate flavor doses for bulk oil factory production. General laboratory duties as required ensuring it runs smoothly and to COSHH recognized safety standards, including making up solutions, arranging waste disposal and correct labeling of chemicals. Assisting New Product Development Any other duties deemed necessary in the department. Operation of GC, UV Spectrophotometer, and Refrectometer for refrective index, Karl Fischer for water, PH meter & testing equipment also use to with titration. Ensuring all Quality and Process Control Standards required for product distribution achieved, manage daily process and product testing & manage all lab documentation, calibration of equipments, monitor and review performance through regular walkabouts and system checks; ensure comprehensive shift record keeping, involved in training and other operational activities as directed by QA managers. Responsible for QA activities on site, supporting the QA Manager and motivating within the QC team.

• Sampling and Testing of Pharmaceutical Raw materials, Processing and Finished product of Tablets, Capsules, Liquids and also Packaging materials.• General handling with lab instruments, magnetic stirrer and balances• Operation of HPLC, GC, UV Spectrophotometer, Karl Fischer, PH meter & testing equipment• Maintain the document of result of raw material & finish products & also S.O.P. (Standard Operating Process) of all QC apparatus.• Verification of validity of data and results • Recording/reporting of data and results• Checking results and entering them into final result sheets• Preparation and labeling of all laboratory reagents, reference standards and solutions properly.• Order chemical and laboratory supplies.