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Company: Acme Lifetech LLP
Location: Export Promotion Industrial Park, Baddi, Dist-Solan HP
Job Title: Regulatory Affairs (Officer to Executive)
Experience Required: 1+ Year in Regulatory Affairs
Qualification Required: M.Pharm (RA)
Application Deadline: 10th August 2024
Application Email: career@acmegrp.in

Responsibilities:

  • Regulatory Compliant Dossier Compilation
  • Documentation Management
  • Licensing & Legal Application
  • Cross-Functional Collaboration
  • Labelling & Artworks Development
  • Sample Management
  • Product Lifecycle Management

Skill Set Required:

  • A strong understanding of regulatory affairs principles, guidelines, and processes of ROW Market
  • Familiarity with the applicable regulations and requirements in the specific industry or country
  • Thorough Knowledge & Experience in CTD & ACTD Dossier
  • Skilled in review of Manufacturing/Analytical/Quality/API DMF Documents
  • Analytical thinking, and excellent organizational and communication skills

Additional Responsibilities:

  • Compare and evaluate offers from suppliers
  • Track orders and ensure timely delivery
  • Enter order details (e.g., vendors, quantities, prices) into internal databases
  • Record of Payment Done

How to Apply: Share your CV to career@acmegrp.in


Post: Regulatory Affairs (Officer to Executive)

Skill set Required:

  • A strong understanding of regulatory affairs principles, guidelines, and processes of ROW Market Compare and evaluate offers from suppliers
  • Familiarity with the applicable regulations and requirements in the specific industry or country Track orders and ensure timely delivery
  • Thorough Knowledge & Experience in CTD & ACTD Dossier Enter order details (e.g. vendors, quantities, prices) into internal databases
  • Skilled in review of Manufacturing/Analytical/Quality/API DMF Documents Record of Payment Done.
  • Additionally, analytical thinking, and excellent organizational and communication skills are highly valued.

Types of Job Roles:

  • Regulatory Compliant Dossier Compilation
  • Documentation Management
  • Licensing & Legal Application
  • Cross-Functional Collaboration
  • Labelling & Artworks Development
  • Sample Management
  • Product Lifecycle Management

Additional Information:

  • Qualification: M.Pharm (RA)
  • Experience: 1 + Year in RA
  • Location: Ahmedabad
  • End Date: 10th August 2024

How to Apply: Share your CV to career@acmegrp.in

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