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Showing posts with the label Pharma Jobs in Telangana

"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs"

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"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs" (Syneos Health Hiring Safety & PV Coordinator in Hyderabad) Introduction Candidates looking to build a strong and long-term career in Pharmacovigilance (PV) and Drug Safety have an excellent opportunity at Syneos Health , a globally recognized biopharmaceutical solutions organization. Syneos Health is currently hiring for the position of Safety & PV Coordinator at its Hyderabad office . This is a full-time, office-based role , ideal for professionals who have experience or exposure in pharmacovigilance submissions, safety reporting, regulatory compliance, and clinical research processes . Working with a global organization like Syneos Health provides exposure to international safety regulations, cross-functional teams, and structured career growth . About The Company – Syneos Health Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports pha...

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“Maithri Drugs QC Method Validation Jobs in Telangana | Apply for Junior Manager, Senior & Junior Executive Roles”

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"Maithri Drugs Hiring for QC Method Validation Jobs in Telangana | Apply Now" (Maithri Drugs QC Method) Are you looking for a career in pharmaceutical quality control ? Maithri Drugs Private Limited, one of the leading pharma companies in Telangana, is hiring for multiple positions in its QC Method Validation Department . This is an excellent opportunity for experienced professionals to grow in a reputed organization while contributing to innovative drug development and regulatory compliance . Job Roles Available:- Maithri Drugs is hiring for the following positions in Sangareddy, Telangana : Junior Manager Senior Executive Junior Executive Key Responsibilities:- As part of the QC Method Validation team , you will be responsible for: Preparing and reviewing incident reports, OOS, SOPs, and investigation reports . Developing and validating method validation/verification protocols as per USP 1225, ICH-Q2 (R1), and ANVISA guidelines. Reviewing chromatograms, audi...

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