Bioanalysis
Bioanalysis
4
Applications
Ahmedabad
Full-Time
Mid-Level: 4 to 6 years
Posted on Mar 25 2025
About the Job
Skills
LCMS
Bioanalytical Validation
BA
Bioanalysis
Goods Clinical Practice
GCP
- On-Site review of Method Development Data and associated procedures
- On-Site review of Method Validation Data and associated procedures
- On-Site monitoring of Bioanalytical Phase
- Incurred Samples Reanalysis, Repeats and Batch Failures
- Investigations during bioanalytical phase
- Preparation of Monitoring Checklist and Report
- Key role in associating with Head of Department for Continuous Improvement Program
- Closely work with Project Managers
- Addressing and fulfilling of client requirements
- Actively participating in new initiatives
- Training to new joiners
- Able to Perform monitoring based on sponsor expectations
- Extensive Travelling would be pre-requisite for this role
- Management of Personal Training Records
About the company
Pharmazone is a leading Consulting company with a strong legacy of trust amongst the global Pharmaceutical & Life Sciences industry. The company specializes in Regulatory Affairs, Pharmacovigilance, GxP Compliance solutions to clients for improving patients lives through unique Commit-Collaborate-Carry Model. As a Regulatory Specialist, we assist our clients with solutions like Regulatory Inte ...Show More
Pharmazone is a leading Consulting company with a strong legacy of trust amongst the global Pharmaceutical & Life Sciences industry. The company specializes in Regulatory Affairs, Pharmacovigilance, GxP Compliance solutions to clients for improving patients lives through unique Commit-Collaborate-Carry Model. As a Regulatory Specialist, we assist our clients with solutions like Regulatory Intelligence & Strategy, Medical Writing, Submission & Publishing, Artwork, Labelling, translation, Health Authority interactions, and all post-approval requirements including an end to end Pharmacovigilance services like case management, Aggregate Reports, Signal Detection, MICC, etc. Our objective is to help large, medium & small-size life science companies in efficient execution & compliance of their drug development plans and Post-Approval Requirements for regulated markets and the developing world. Global Regulatory Landscape is dynamic and our compliance services (GXP) play a vital role for clients. Being a trendsetter in GCP Auditing & Consulting, Pharmazone has successfully carried out 2000+ projects for Clinical Monitoring (Bioequivalence, Late Phase), Study Design, Audits, CRO setup & Up-gradation & Programme Management. Our GMP Solutions include Audits, Report Library, Quality Consulting, USFDA/EMA/PICS/WHO accreditation Support, CSV & Engineering Services including Plant Setup & Upgradation. Though Client's trust is our biggest recognition, our hard work-filled journey has brought us various awards like "Best HealthCare Brand" by CMO Asia -ABP News, Top 10 Clinical Research Provider by Silicon India. "Value Creation by Right solutions is Working Mantra at Pharmazone. The expert team at our global locations (INDIA, USA, CANADA and CHINA) have served 300+ Clients to satisfaction and we look forward to serving you! ...Show Less
Industry
Pharmaceutical Manufactur...
Company Size
51-200 Employees
Headquarter
Ahmedabad
Other open jobs from Pharmazone