Freshers & Experience Bsc,Msc,Bpharm,Mpharm for Multiple Positions At ADVITY RESEARCH Pvt Ltd

ADVITY RESEARCH PRIVATE LIMITED Walk-in Interview 2024.ADVITY RESEARCH PRIVATE LIMITED Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.

Vacancy details:

• Department: Join us for inclusive growth Analyst – Bioanalytical (LC-MS/MS) Analyst – Bioanalytical (ELISA / LBA) CRA / CRC / Monitoring – Clinical Trials Clinical Trials – QA Medical Writer Manager Business Development – Clinical Trials Clinical QA Auditor – BA/BE Manager Business Development – Pharmacovigilance Drug Safety Associate – MICC Safety Writer – Aggregate Reporting (AR) Senior Drug Safety Associate
• Experience:0-5   years
• Qualification: B Pharm/BSc in Life Science/M.Pharm/MSc in life Scinece
• Salary:₹Not Disclosed

Important Details :

• Location: Hyderabad
• Post of date :26/12/2024
• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Job Description: Greeting from ADVITY RESEARCH PRIVATE LIMITED .!!!!!

Preferred Skills:

Qualification: M.Sc. / B.Pharm / M.Pharm

Handling experience on LC-MS/MS

Extensive experience on MD/MV of Bioanalytical Methods

Well versed with bioanalytical, GLP regulations for handling bioanalytical projects

Job Description:

Perform method development, method validation and study sample analysis in compliance with applicable methods, protocols, SOPs, and regulatory guidelines.

Operation of key bioanalytical equipment’s like HPLC, LC-MS/MS and ELISA

Perform sample analysis and compilation of data in timely manner in line with applicable SOPs.

Responsible for compliance to relevant audit findings from QC/QA and take appropriate actions in relation to audit findings with guidance of project Incharge/ group leader.

Preparation of Standard Operating Procedure (SOPs), Method SOPs, bioanalytical protocols/plan, method validation reports and bioanalytical study reports.

Archival of method and study related documents after completion of QA review.

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