Job Description

Major Purpose: (Exactly spell out key deliveries/results expected from this job) o To follow proper gowning / De-gowning procedure as per SOP. o To follow all respective SOPs & BMR procedure in the department and during operation. o To do the cleaning of Capsule filling machine, Shorter, Polishing machine, metal detector, check weigher, inspection machine and its cubicle as per SOP. o To check and ensure the cleanliness of Capsule cubicle, equipment and environmental Condition (Eg:- tempreture,RH and pressure differential) within specified limit before Start and during Capsule filling process. o To check and ensure proper operation of the capsule filling machine in Capsule area. o To carry out in-process checks during Capsule filling operations as per MMD I. o To manufacturing the product on time which complies the regulatory and marketing requirement. o To monitor the capsule filling machine and operation without affecting Quality of product. o To maintain all the log books & records where ever necessary. o To check and ensure proper labelling of equipment, area and product in manufacturing area. o To ensure that proper maintenance and safety of person and equipment's. Responsibilities: o To follow the departmental SOP, s as per GMP requirement. o To Check and ensure the coated tablets should be kept in WIP area under lock & key as per SOP. o To check and ensure the cleanliness of Capsule cubicle, equipment and environmental Condition (Eg:- tempreture,RH and pressure differential) within specified limit before Start and during Capsule filling process. o To keep the area ready for line clearance. o To do the physical verification of empty and filled Capsules as per MMD-I in presence of Production & verified by QA person. o To do the proper and maximum utilization of machines. o To Check and ensure about that the process should be as per BMR, if any deviation it should be informed to supervisor. o To Complete Manufacturing and capsule filling Operation with in time & keep the empty and filled capsule in WIP area & maintain its record. o To reduce breakdown time through proper handling and maintenance of the machine. o To maintain the online documentation as per GMP guidelines. o To clean and maintaining equipment change part and records as per requirements. Environment and Health & Safety o To ensure that Zero accident & Zero tolerance in the area. o To ensure use the correct PPE, s. o To participate in various Awareness trainings on Environment, Health and Safety. CFT Meeting : o Regularly attend the sop,s training as per the plan. o Participate in resolving the issues in the CFT being a team member, and helping to resolve machine related issues. Principal Accountability: o To maintain quality and productivity. o To ensure that Zero accident & Zero tolerance in the area. o To follow all respective SOPs, BMR procedure & Discipline in the department & Operation.