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Private Jobs / Private Sector
Piramal Enterprises Hiring for Executive – Sevoflurane (Documentation) at Telangana Full Time
Full Job Description
To follow and maintain cGMP standards in production areas/activities.
To follow day to day production schedule and ensure to complete the production activities as per schedule.
To take & follow instructions from Superior/Manager.
To maintain manufacturing records online & should comply data integrity practices.
Responsible to maintain housekeeping in plant & take care the cleanliness of equipment.
Responsible to carry out the work of his senior in the absence of senior or authorization from senior.
Responsible for GMP verification and compliance review.
Responsible for allotment of work to team members.
Responsible for documentation activities such as Change controls, Deviation, Investigations, Market Complaint Investigation, CAPA, Preparation & review of protocols, SOP’s, revision of SOP’s, Batch record preparation, review, and submission, provide trainings on documentation.
Co-ordinate with relevant Cross functional departments (QA, QC, SCM, E & M, EHS, HR, etc.) and reporting manager for various production related activities and smooth flow of documentation.
Handling of External and Internal Audits, Safety Audits, Visits, and their compliance.
Responsible for maintaining online SAP entries and other SAP activities.
Follow safety instructions/procedures & ensure use of safety outfit while on works.
To attend GMP & safety trainings & implement the trainings outcome at work place.
Should be aware of the location of firefighting equipment and should know the operation.
To involve in other initiatives such as AET & CSR.
To follow day to day production schedule and ensure to complete the production activities as per schedule.
To take & follow instructions from Superior/Manager.
To maintain manufacturing records online & should comply data integrity practices.
Responsible to maintain housekeeping in plant & take care the cleanliness of equipment.
Responsible to carry out the work of his senior in the absence of senior or authorization from senior.
Responsible for GMP verification and compliance review.
Responsible for allotment of work to team members.
Responsible for documentation activities such as Change controls, Deviation, Investigations, Market Complaint Investigation, CAPA, Preparation & review of protocols, SOP’s, revision of SOP’s, Batch record preparation, review, and submission, provide trainings on documentation.
Co-ordinate with relevant Cross functional departments (QA, QC, SCM, E & M, EHS, HR, etc.) and reporting manager for various production related activities and smooth flow of documentation.
Handling of External and Internal Audits, Safety Audits, Visits, and their compliance.
Responsible for maintaining online SAP entries and other SAP activities.
Follow safety instructions/procedures & ensure use of safety outfit while on works.
To attend GMP & safety trainings & implement the trainings outcome at work place.
Should be aware of the location of firefighting equipment and should know the operation.
To involve in other initiatives such as AET & CSR.