AURA - BE/BM-JAIPUR 1
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
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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. 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. 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. Build
To initiate and perform the QMS activity. Handling Deviations, CAPAs and Change Controls. Performing IQ, OQ and PQ activities of vial and ampoule filling machine. To prepare the SOPs, BMR, Protocols a
Responsible for Packaging material receipt, issuance and Dispensing & planning. Responsible for Inventory management of Packaging material. Responsible for Verification and Calibration of weighing Bal
To initiate and perform the QMS activity. Handling Deviations, CAPAs and Change Controls. Performing IQ, OQ and PQ activities of vial and ampoule filling machine. To prepare the SOPs, BMR, Protocols a
To initiate and perform the QMS activity. Handling Deviations, CAPAs and Change Controls. Performing IQ, OQ and PQ activities of vial and ampoule filling machine. To prepare the SOPs, BMR, Protocols a
To initiate and perform the QMS activity. Handling Deviations, CAPAs and Change Controls. Performing IQ, OQ and PQ activities of vial and ampoule filling machine. To prepare the SOPs, BMR, Protocols a
Manufacturing Having Knowledge of Good Manufacturing practice in API Plants. Knowledge of Equipment Cleaning. Having knowledge of Reactor, Vacuum Pump, Distillation and All other parameter related to
1. Compliance & Regulatory Adherence - Ensure adherence to GPV, GCP, SOP, Protocols, and ethical guidelines. 2. SOP Management - SOP review and Management 3. Training and process improvement: Training
Product Development of Oral Solid Dosage Forms . Basic knowledge about different pharmaceutical dosage forms. Writing/reviewing Standard Operating Procedures (SOPs) , Observing and complying with Good
Product Development of Parenteral Dosage Forms . Basic knowledge about different pharmaceutical dosage forms. Writing/reviewing Standard Operating Procedures (SOPs), Observing and complying with Good
EHS (ETP), Should have experiecne in Lab with ETP and safety Should have experiecne in Lab with ETP and safety Should have experiecne in Lab with ETP and safety
Validation/Qualification activities ➢ Handling and leading QA validation activities (Which include Scheduled Requalification, New qualifications/validations due to Change control or new projects, New
Basic knowledge of, wet chemistry, spectroscopy and chromatographic techniques. Sound theoretical knowledge of analytical instruments like High performance Liquid Chromatography (HPLC), Gas Liquid chr
Sr. Officer / Executive -Export Pre & Post Shipment documentation , Invoicing , LC documentation ,Verification of Checklist, E-mail communication with Customer/ CHA/Forwarder/Internal team, Tracking o
Sr. No. Responsibilities 1.0 Work allocation for LIMS Department. 2.0 Review Documents in LIMS Software for All location 2.1 Review of Finished product , Raw Material and In process Specification, MOA
Manufacturing API Production Bulk drugs & Reactor handling BMR & BPC Filing Production & Manufacturing
Evaluate and qualify new vendors based on product, service, and compliance requirements. Conduct vendor audits (onsite or remote) to assess quality systems and GMP compliance. Maintain and update the
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