Gujarat

The Clinical Data Management Associate is responsible for providing expert skills as part of the clinical data management team within the Data Management and Statistics Department to ensure that efficient and quality data management products are produced in accordance with customer requirements.

Expertise in different types of purification techniques. Sound knowledge of different column chemistry used in HPLC. Responsible for troubleshooting of instruments and their calibration

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

M.Sc./ M.Tech./ M.Pharm./ B.Tech. or equivalent in Biotechnology and allied areas; Research project entitled Targeting Autophagy and Microtubule Dynamics for Next- Generation Cancer and Neurovegetative Disease Treatment funded by Gujarat State Biotechnology Mission, Govt. of Gujarat.

B.Pharm / M.Pharm; Compile, review and timely submission of Deficiencies responses as received from Health Canada. Support Cross-functional team like Analytical Development, Formulation Development during product development and align documentation as per HC guidelines.

SCIENCES OR PHARMACY GRADUATES B.SC, M.SC, B. PHARM, M. PHARM WITH 0 TO 5 YEARS EXPERIENCES IN PARENTERAL MANUFACTURING VIAL, AMPOULES, BOTTLES OF GLASS OR PLASTIC THROUGH, LVP/SVP WITH BFS TECHNOLOGY. CANDIDATE WORKED IN PRODUCTION COMPLIANCES, REMEDIATION AND HAVING EXPERIENCES OF MANAGING QUALITY SYSTEM DOCUMENT

Responsible for QMS Team lead for Block, Exposure to US, EU and CA regulatory requirements, Handling of market complaint

Handling of Analytical Instruments Like HPLC, LCMS, GC, Prep HPLC, SFC, Prep SFC, KF and SOR along with software. Method development by HPLC, GC for RM, Intermediate and final product.

Ensure ALCOA compliance, SLA adherence. Handle HPLC, UPLC, LCMS, GC, GCMS, Dissolution. Oversee method transfers & regulatory compliance.