Executive QA (Validation) - V'Nagar
Preparation of Qualification protocol and report Review of document and compilation of document execution of qualification documents
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Preparation of Qualification protocol and report Review of document and compilation of document execution of qualification documents
Review of change control ,deviation, OOS and OOT documents Assign change control, deviation and CAPA to user department involve in investigation and market complain Self inspection management and plan
Analysis of Drug Product using HPLC, Particle size analyzer, Autotitrator, Chcmical testing, Documentation. Knowledge of LIMS.
Experience of documentation, calibration of instrument & equipment, LIMS, chemical testing, working standard qualification.
Legal Compliance pertaining to Environment Health and Safety Operations of ETP, STP, MEE, Laboratory and Hazardous Waste Area. GMP Documentation pertaining to EHS Department. Environmental Monitoring
Plant round to check the gaps and report to HO Report incident along with investigation and corrective and preventive action of near miss/incident/accident. Monitoring of work permit system at site an
Review of batch manuafcturing record and line clearance of area and equipment Inprocess check and sampling of bulk , finshed product AQL sampling . Packing and manufacturing sampling.
To perform accurate and reliable analysis of Raw Material as per method of analysis or protocol. To perform method transfer, method verification, analytical method validation and protocol base study.
Sr. No. Responsibilities 1.0 Documents review and approved 1.1 Finished product:- Approved COA, electronic data review checklist, raw data, worksheet, working standards/reference standards details, in
Sr. No. Responsibilities 1.0 Line Clearance activity. 1.1 Line clearance of area and Equipments as per checklists of SOP/ batch records at various stages of dispensing, manufacturing and packing activ
Sr. No. Responsibilities 1.0 Handling of Overall QMS (Quality Management System) activities 1.1 Change Management 1.1.1 Initiation of Change control for QMS related changes, implementation and closure
Sr. No. Responsibilities 1.0 Issuance and Retrieval of Log Book and Loose Annex. 1.1 Issuance and Retrieval of Log book as per request given by concern department. 1.2 Issuance and Retrieval of Loose
Sr. No. Responsibilities 1.0 Handling of Signature Log. 1.1 To maintain signature log for New Employee and Left Employee. 2.0 Document Preparation. 2.1 To prepare the qualified trainer list. 2.2 To pr
Sr. No. Responsibilities 1.0 Issuance and Retrieval of Log Book and Loose Annex 1.1 Issuance and Retrieval of Log book as per request given by concern department. 1.2 Issuance and Retrieval of Loose A
Plant maintenance Must have experiecne in PLC and scada Local candidates are preffered. Local candidates are preffered. Local candidates are preffered.
Team Management: • Leading, Coaching and Motivating the Business Managers • Maintain good bonding with teammates to ensure smooth deliverance of objectives and arresting attrition • Sustained efforts
Promoting products: • Promote the company's products to Doctors, Retailer/pharmacist • Discuss the clinical usage, dosages, and how our products/brands can be used to treat different conditions. Build
Team Management: • Leading, Coaching and Motivating the Business Managers • Maintain good bonding with teammates to ensure smooth deliverance of objectives and arresting attrition • Sustained efforts
Promoting products: • Promote the company's products to Doctors, Retailer/pharmacist • Discuss the clinical usage, dosages, and how our products/brands can be used to treat different conditions. Build
Promoting products: • Promote the company's products to Doctors, Retailer/pharmacist •Discuss the clinical usage, dosages, and how our products/brands can be used to treat different conditions. Buildi
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