Aurobindo Pharma

Job Description • Testing of Raw materials, In-process, Intermediates and APIs using Chromatographic Data system. • Analytical Testing of Related substances/Content/Assay/Purity testing and Calculation by HPLC Using Empower/Lab Solutions. • Data generation, Integration and Review of Chromatographic data generated by Chromatographic data system. • Method Transfers & Holding time Studies. • Stab

Job description Lifecycle management on specific products for Europe and international market Responsible at all times that regulatory modules under Product Manager responsibility are up to date, in accordance with agreed procedure as applicable Inform, prepare and submit variations either directly to authorities or to Teva s 3rd party client business (Medis) Follow up on variation submission

Responsibilities: coordinate all quality actions follow the GMP associated with the products / processes on which you work ensure the control of raw materials, packaging items and / or finished products plan the analyzes to be carried out validate the specifications examine returned products and complaints control the application of protocols and regulations write quality control procedur

Responsibilities: Ensure all phases of a manufacturing and other handling process meets the standards or requirements of the quality plan including in-process check. Play an active role in all stages of the production process (Raw Materials Analyst), during production itself (In Process Analyst) or at the end of manufacture (Finished Product testing). Timely completion of all experiments accordi

Responsible for the execution of Production plan and managing the use of man power for multiple shifts, coordination between various departments. Maintenance compliance of all equipments. Monitor and manage staff to meet deadlines & commitments

About The Internship • Aurobindo Research Centre is providing an opportunity for M.Pharmacy Freshers to gain the industrial knowledge through its 9 months internship in the below R&D Areas Formulations R&D (OSD) • M Pharmacy -Pharmaceutics as Specialization (2021 & 2022 Pass outs only) Formulations Analytical R&D (Derma) • M Pharmacy -Pharmaceutical Analysis as Specialization (2021 & 2022

Function: Packaging Industry: Pharma/Biotech/Clinical Research Location: Telangana

Day to Day Management along with the Paramedics - Identification of occ. health hazards at the plant across various shop floors - Identification of notifiable diseases (is any) as per the schedule II of the Factories Act - Address medical problems of the workers as well as any industrial health related problems i.e. monitoring hazards, use of PPE, biological monitoring, etc. - Cond

Formulation Development and Optimization of Solid Formulations. Handling of Regulatory Queries. Responsible for maintenance of assigned lab equipments. Education Qualification for the position M.Pharma

JOB DESCRIPTION: You will be responsible for preparing and reviewing technical documents for ANDA/dossier submissions in various countries. You will need to format these documents according to CTD, ACTD, and country-specific guidelines and coordinate with other departments for any necessary technical or administrative documents. Additionally, you will be responsible for creating clear pr

Roles and Responsibilities 1) To prepare dossiers for product registration, renewal and variation applications in African, Middle East countries ROW Countries in Regional as well as CTD formats as per the requirements for registration purpose. 2) To check artworks for regulated/ semi regulated countries. 3) To co-ordinate for documents and samples for regulatory submissions with manufact

Formulation Development and Optimization of Injectable Formulations. Execution of Scale Up and Exhibit Batches. Preparation of Technology Transfer Documents. Preparation of Product Development Reports. Handling of Investigations of OOS. Handling of Regulatory Queries. Responsible for maintenance of assigned lab equipments and preparation of SOPs of the same.

Person having knowledge in Regulatory Affairs in Nasal Dosage form-US Market is suitable for this position. Education Qualification for the position: B.Pharma/M.Pharma

JOB Responsibilities: 1.1. To ensure the preventive Maintenance Plan of all instruments in 'Injectable & OSD lines' according to Master Calibration plan 1.2. To Perform Breakdown Maintenance of all QC analytical instruments 1.3. Ensuring sufficient inventory of all instrument spares 1.4. Shall be responsible for administrative activities of Empower software and Standalone software

Responsibilities: Draft quality assurance policies and procedures Interpret and implement quality assurance standards and procedures Evaluate adequacy of quality assurance standards Devise sampling procedures and directions for recording and reporting quality data Review the implementation and efficiency of quality and inspection systems Plan, conduct and monitor testing and inspection of p