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Regulatory Affairs - Executive/Officer Arch Pharmalabs Ltd - Mumbai, Maharashtra filingKnowledge of analytical validationKnowledge of QC/QA systemsKnowledge of regulatory guidelinesReview of analaytical specification and process validation... TimesJobs.com - 1:26 AM Officer - Drug Regulatory Affairs (ANDA) Famy Care Pvt ltd - Navi Mumbai, Maharashtra Job DescriptionResponsible for registration of products in regulated market such as US/EU, should able to compile dossiers for regulated market in CTD / eCTD... TimesJobs.com - 1:25 AM Assistant Manager / Executives Regulatory Affairs [APIs & Granulation Sri Krishna Pharmaceuticals Limited - Hyderabad, Andhra Pradesh To lead / assist a group of professionals, who would be involved in QA related activities as per the TGA/USFDA norms Naukri.com - 5:27 AM Require regulatory affairs manager at Rhydburg Pharmaceuticals Ltd. Rhydburg Pharmaceuticals Ltd. - Delhi, Delhi Responsible for coordination, preparation, compilation and submission of regulatory dossiers, which shall include preparation of dossiers for CIS, Asian and... Jobsindia.com - 10:11 PM Manager - Medical Affairs Mancer Consulting Services - Mumbai, Maharashtra for regulatory submission. Helping in resolving the queries from the regulatory. To assist the regulatory affairs personnel in ensuring that all promotional... Careesma - 5:31 PM Assistant Manager - Regulatory Affairs & Quality Assurance 3M India Limited - Pune, Maharashtra As per the regulatory requirements, we need to have a... supplier evaluations. 5) Ensure compliance to Regulatory requirements for the Medical plant, specifically... Naukri.com - 5:33 AM Head - Formulation Development Talent Forte - Baddi, Himachal Pradesh transfer for Regulatory Markets ROW Markets... filing knowledge and documentary support to Regulatory Affair for preparation of EU CTD and ACTD dossiers... TimesJobs.com - 1:25 AM New Hope Pharmacovigilance - Level B, General Manager [5647] 2COMs - Chennai, Tamil Nadu strong communication skills. Strong knowledge of Pharmacovigilance, and exposure into regulatory affairs, adverse events, serious Adverse events are a must... 2COMs - 7:39 AM |
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