Drug Regulatory Affairs Officer

**Responsibilities**: 1.Drug related Conduct of clinical studies, data collection, statistical analysis, report writing Keeping track of changing legislation in regions where the company distributes its products. collect, collate and evaluate scientific data from a range of sources. To give strategic and technical advice to R&D, production, QC department,...

Regulatory affairs 4+ years of experience agrochemical/pesticide. Experience with regulatory submissions, dossier preparation, and interactions with regulatory authorities. Ellora park vadodara Pay: From ₹12,000.00 per month **Experience**: - total work: 1 year (preferred) Work Location: In person Application Deadline: 30/01/2025 Expected Start...

Job Title: Senior Regulatory Affairs SpecialistAbout the RoleWe are seeking an experienced and skilled Senior Regulatory Affairs Specialist to lead our regulatory activities for USFDA submissions, including preparation, review, and filing of documents.The ideal candidate will have a strong understanding of ICH, USFDA guidelines, and regulatory frameworks...

Requirement of Regulatory Affair- ManagerIndustry - Pharma/Healthcare(Only for Male)Address:-Diamond Heritage Building,BBD Bag, Kol-700001Job Role: Regulatory Affairs-Manager/Asst.ManagerSalary: Negotiable (No PF & ESI,only P-Tax deduction)Qualification: - · Bachelor's or Master's degree in Pharmacy, Life Sciences, Chemistry, or related discipline.Key...

**Responsibilities**: i. Legal Advisory & Compliance ii. Litigation Management iii. Contract Drafting & Negotiation iv. Risk Management v. Regulatory Compliance & Policy Implementation vi. Handling Disciplinary & Grievance Matters vii. Intellectual Property Rights (IPR) Protection viii. Documentation & Record-Keeping ix. Coordinating with government...

Regulatory Affairs SpecialistWe are seeking a detail-oriented Regulatory Affairs specialist to support end-to-end submissions for global markets.The ideal candidate will have experience in managing Initial submissions, Variations, and full Lifecycle Management deliverables for the global markets. They must have hands-on experience with Veeva Vault RIM and...

JD's :Regulatory Strategy: ROW Market Expansion,CTD/eCTD Dossiers,Registrations,Renewals,Variations,CDSCOCompliance & Audits: Regulatory Audits,Inspections,Artwork Compliance,Promotional Materials,Risk MitigationMail-Annual bonus

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science - bringing creative ideas, products and services to advance the health and well-being of people. Every day, our more than 130,000 employees across the world are blending heart, science and ingenuity to...

Regulatory Affairs ProfessionalWe are seeking a seasoned Regulatory Affairs Specialist with expertise in pharmaceutical and medical device regulatory compliance to join our team.Key Responsibilities:Prepare, review, and submit regulatory filings for global health authorities.Ensure compliance with international, federal, and local regulations across...

**Responsibility**: - Manage transportation schedules and vehicle dispatch, especially for night shift coverage. - Coordinate with drivers and vendors to ensure timely and safe employee drop-offs, in compliance with IN labor law. - Serve as a backup transportation/fleet manager during night shifts. - Perform general administrative and logístical support...