Regulatory Affairs Jobs in Kolasib
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Search Results - Regulatory Affairs Jobs in Kolasib
ProductLife Group-Kolasib
experience:
Minimum of 3 years of experience in regulatory affairs Preference for experience in Australian and New Zealand in a commercial environment.
Required language: English
Required technical skills:
• Good knowledge of TGA and Medsafe legislation...
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vueverse.-Kolasib
R&D, Quality, Clinical, and Manufacturing.
• Monitor regulatory changes and assess impact on ongoing projects.
Requirements:
• 8+ years of experience in medical device regulatory affairs.
• Bachelor's degree or higher in Biomedical Engineering, Life...
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vueverse.-Kolasib
Role Overview
We are seeking a Regulatory Affairs Specialist - Nutraceuticals/Food Supplements to lead global regulatory strategy and execution for multi-market product registration projects. This role serves as the primary regulatory expert...
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P360-Kolasib
regulatory data harmonization and governance
• Collaborate with Regulatory Affairs, IT, and external partners
• Support inspections, audits, and health authority submissions
• Provide functional leadership across multiple RIM workstreams
Required...
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Greymatter Innovationz-Kolasib
standards
Collaborate with Marketing, Legal & QA teams
Requirements: 5+ years in Regulatory Affairs / RIM (Pharma / Life Sciences)
Hands-on with Veeva Vault, ArisGlobal, or similar
Strong knowledge of labeling & promotional compliance
Excellent stakeholder...
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Cytel-Kolasib
Development, Data Management, Biostatistics, Regulatory Affairs, and IT to align digital strategy.
• Represent the organization in industry working groups or standards forums as appropriate.
• Provide training and knowledge-sharing sessions on USDM and Digital...
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P360-India
responsible for driving integrated Vault solutions across Regulatory, Quality, and Medical Affairs.
Key Responsibilities
• Lead multi-module, cross-functional Vault programs
• Define enterprise Vault architecture and integration strategy
• Align regulatory...
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Planet Pharma-Kolasib
functional expertise including Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome...
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