Junior Data Analyst – Pharmacovigilance – Fresher

Education: B pharm/M pharm fresher Location: Mumbai Designation: Junior Data Analyst Job description: knowledge on Med DRA Track all adverse event reports received and completed; Review and assess all source documents, and compile data in an adverse event report; Data enter report into the client safety database; Code adverse events in the client safety database;…

Apply Here >>

Walk-in Drive for Analytical – 22nd April @ Syngene bangalore

Walk-in Drive for Analytical – 22nd April @ Syngene bangalore Job Description Analytical R&D M. Pharm/ M Sc from reputed institutes with experience in Analytical R&D for Formulation Development Skill set required : Expertise in Analytical Method development, Method Validation, Method transfers and stability studies (expertise in Analytical R&D for Formulation development Solid Orals and…

Apply Here >>

Opening for Officer / Executive QC (hplc) for Usfda Plant Panoli. – 30 Opening(s) @ JBCPL

Opening for Officer / Executive QC (hplc) for Usfda Plant Panoli. – 30 Opening(s) @ JBCPL Job Description: Must have good Experience of Sample Analysis by HPLC System. Experience 1 – 6 Years Education UG – B.Pharma – Pharmacy, B.Sc – Chemistry PG – MS/M.Sc(Science) – Any Specialization, Chemistry, M.Pharma – Pharmacy Doctorate – Compensation:…

Apply Here >>

Work as a Safety Associate Trainee @ QuintilesIms

Work as a Safety Associate Trainee @ QuintilesIms Description PURPOSE Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. RESPONSIBILITIES To Prioritize…

Apply Here >>

Regulatory CMC Associate Job @ Novartis

Regulatory CMC Associate Job @ Novartis Post : Reg CMC-Associate Manager-I/II Job Description : 1. Author high-quality CMC documentation for HA submission, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle. 2. Prepare CMC responses to health authority…

Apply Here >>