Dynamic production supervisor in pharmaceutical industry with more
than five year experience supervising three production lines, overseeing
materials inspection, involving in initial qualification, validation and media fill activities, scheduling production, focused on producing high quality
products and help achieve company production and revenue goals.
Good Aseptic and Clean Area
Production Line Management
Material Handling Expertise
Man Power Handling
Quantitative and Data-analysis skills
Communication and Team Work
Handling Media Fill Activities
Monitoring Samples for QC in Various Batches and Media Fill
Qualification of Various Machines like Autoclave, PPM washing and Depyrogenation Tunnel, Filling and Capping Machine etc.
08/2011 to 09/2016
Sr. Officer (Parenteral Production Department)Sun Pharmaceutical Industries LTD. (Unimed Technologies LTD.) – Baska, Halol, India
Supervised various manufacturing
activities i.e. Equipment preparation & Sterilization, Batch
filtration, filling, lyophilization, capping, and storage in allocated
shifts and ensured process adherence as per SOPs.
Verified that all process control
parameters were being documented and followed at all times.
Planned, directed, coordinated and
assigned manpower to meet production schedules and to achieve optimum
Procured required manufacturing equipment
and parts for the process and ensured their qualification and calibration
Prepared various documents like SOP, Change Control, Event & Investigation Report, Qualification and
Validation Protocol, BMR etc.
Media Fill activities at various stages of production.
monitored sampling in various Process Validation and Cleaning Validation
Ensured status labels on area/
equipments/ services/ products of related area at each stage.
Production Planning and Availability, Engineering services, Quality Assurance
& Quality Control for smooth functioning of the process.
Qualification and Validation activity of various equipments and the area.
Completed and maintained accurate and organized records, documents and reports.
Recommended and executed quality
improvements for production and product quality.
Created and updated department work
instructions and reports on a regular basis.
Ensured training of cGMP and SOPs to
sub-ordinates periodically as per defined schedule.