Job Description
Research Associate-Analytical Method Validations (Respiratory)
Roles and Responsibilities:
This roles is based out Glenmark’s Aurangabad Manufacturing plant and involves supporting R&D team with Analytical Validations and Development process of Respiratory portfolio dosage forms (Inhalers, Aerosols of various indications, Nebulizers, Tablets / capsules etc.) for Global Markets. The goal of this role is to deliver services with an accuracy in results and within agreed timelines set by Group leader.
•Perform Method Validation at Manufacturing Plant and R&D site – Ensure that all tasks assigned by the functional manager/Seniors are completed within time and with appropriate quality. Conduct/Execute validation activity as per protocol. Daily online calculation of validation related activity. Prepare Validation Protocol and Report as per guideline and regulatory requirement Calibration and qualification of Instruments – Ensure that all tasks completed as per SOP and according to GLP procedure within time. Follow current GLP System in the lab maintain the quality and accuracy of the work throughout the year.
Desired Candidate Profile:
Education (Degree/ Diploma) : M.Pharm – Pharmaceutics Chemistry / Ph. D / M.Sc. Analytical Chemistry
Experience: Should have 2-6 years total work experience in Analytical Method Development
Knowledge & Skills ( Functional / Technical): Should be well acquainted with handling below equipment like HPLC/UPLC/Spray View etc.
Other requirements (licenses, certifications, specialized training) – Experience in handling ANDA
Interested Candidates who meet the above criteria can send their CVs to (Dhurjuti.Dhibar@glenmarkpharma.com) and Bhushan Wadgaonkar (Bhushan.Wadgaonkar@glenmarkpharma.com)
Location: Nashik / Aurangabad
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