QMS Executive

DescriptionResponsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements.Responsible for document management and preparation like BMR's, BPR's, master SOP's etc.Responsible for the handling of change control, deviations,...

DescriptionKey Responsibilities: Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements.Responsible for document management and preparation like BMR's, BPR's, master SOP's etc.Responsible for the handling of...

Company Description Continental develops pioneering technologies and services for sustainable and connected mobility of people and their goods. Founded in 1871, the technology company offers safe, efficient, intelligent and affordable solutions for vehicles, machines, traffic and transportation. In 2024, Continental generated sales of €39.7 billion and...

Company Description Continental develops pioneering technologies and services for sustainable and connected mobility of people and their goods. Founded in 1871, the technology company offers safe, efficient, intelligent and affordable solutions for vehicles, machines, traffic and transportation. In 2024, Continental generated sales of €39.7 billion and...

Company Description Continental develops pioneering technologies and services for sustainable and connected mobility of people and their goods. Founded in 1871, the technology company offers safe, efficient, intelligent and affordable solutions for vehicles, machines, traffic and transportation. In 2024, Continental generated sales of €39.7 billion and...

DescriptionMaintain and follow the procedure as per SOP in day to day activity of warehouse.Receipt of materials, Physical verification and Preparation of Good Receipt Note in ERP systems and mail to concern user and purchase department.Affix status label (Quarantine) on all received materials and movement as per status updating.To update the record as per...

DescriptionResponsible for document management like BMRs, BPRs, master SOPs etc.. Responsible for preparation & review of the master documents of production. Responsible to ensure UAF working in area. Responsible for the handling of change control, deviations, investigation & CAPA, etc.  Responsible for line clearance activity before commencing the...

DescriptionKey Responsibilities:•Sterile / Parenteral / Aseptic•Filling, Sealing, Filtration, Production QMS•Batch Manufacturing•Autoclave•Terminal Sterilization•Packing & Visual InspectionQualificationsQualification Requirement: B.Pharm / M.ScExperience: 2-7 years  

DescriptionKey Responsibilities: • Material Receipt & Verification — Oversee material receipt, verification, labelling, and GRN preparation in ERP. • Storage & Inventory Management — Ensure proper storage, stock updates, and scheduled physical verification. • Material Issuance & Dispensing— Manage material dispensing as per BMR/BPR and...

DescriptionResponsible for document handling, issuance, distribution, and retrieval of docume,verification of documents like Batch Manufacturing records, Batch Packaging Records, Protocols, layouts, specifications, Method of Analysis, Logbooks, Planner, etc. Responsible for issuance of approved Standard Formats and Logbooks to User Departments, Issuance of...