Regulatory Affairs Job opportunity at Acme Lifetech LLP- Apply before 10th August 2024

ACME Pharmaceuticals

Website Acme Lifetech LLP

About Acme Lifetech LLP

Acme Lifetech LLP is a newly constructed, research-oriented formulation site located in the Export Promotion Industrial Park, Baddi, Dist-Solan HP. Situated in a non-polluting zone, this state-of-the-art facility is just 50 km from Chandigarh Airport. Acme Lifetech LLP is designed to meet evolving international regulatory trends and requirements, offering integrated solutions for contract manufacturing operations in both domestic and global markets.

Position: Regulatory Affairs (Officer to Executive)

Skill Set Required

  • Strong understanding of regulatory affairs principles, guidelines, and processes for the ROW Market.
  • Familiarity with applicable regulations and requirements in the specific industry or country.
  • Thorough knowledge and experience in CTD & ACTD dossier preparation.
  • Skilled in the review of Manufacturing/Analytical/Quality/API DMF documents.
  • Analytical thinking, excellent organizational and communication skills.

Types of Job Roles

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

Additional Information

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

How to Apply

Share your CV at: career@acmegrp.in

Join us at Acme Lifetech LLP and be part of a cutting-edge team dedicated to excellence in pharmaceutical research and manufacturing.

To apply for this job email your details to career@acmegrp.in