We are looking for a professional with experience in Analytical_Research & Development department with expertise in LC_MS Executive Level Apitoria_Pharma Private Limited, a 100% subsidiary of Aurobindo_Pharma Ltd., based in Hyderabad.
Position Details-
- Designation: Executive / Senior Executive
- Department: Analytical Research & Development (AR&D) LC-MS
- Role: Team Member
- Location: Hyderabad
Educational Qualification : M.Sc. in Chemistry / M. Pharm in Pharmaceutical Analysis
Experience : 3 – 7 years of relevant industry experience in Analytical R&D, with strong expertise in LC-MS.
Required Skill Set:
*Strong communication, interpersonal, and presentation skills.
*Experience in LC-MS Method Validation, Method Development and Batch analysis.
Key Responsibilities:
1. Responsible for LC-MS/MS method development, method validation and batch analysis.
2. Impurity profiling for identification of unknown impurities in small molecules.
3. Calibrations of instruments as per calibration SOP.
4. Supporting to Routine and LC-MS analysis.
5. Following proper documentation as per GDP.
6. Following GLP and regulatory requirements.
7. Maintaining the lab clean and neat as per GLP & Safety measurements.
8. Knowledge of current guidance documents issued by regulatory agencies.
How to Apply:
Interested candidates with relevant experience may apply by scanning the QR code provided in the poster.
We are looking for candidate with experience in #RAD_Department at #Executive level #Apitoria Pharma Private Ltd., (100% subsidiary of #Aurobindo Pharma) located at Hyderabad.
Requirement Details:
Qualification: MSc Chemistry.
Experience: 3-6 Years
Designation: Executive / Senior Executive
Department: Regulatory Affairs (RA)
Required Skillset :
*Experience in Drafting, reviewing module-3 of API.
*Good understanding of life cycle management in API Regulatory Affairs.
*Clarity on regulatory Guidelines, Documents on Post Approval changes.
*Good communication and presentation skills.
Key Responsibilities:
*Evaluation of the change controls.
*Drafting and sending the change notification to customers till its implementation.
*New submission – DMF compilation and submission to global health agencies.
*Life Cycle Management – Amendments and Revisions – compilation and submission to global health Agencies
Interested candidates with relevant experience can apply by scanning the QR code given in the poster.
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