Regulatory affairs

Academic degree in Pharmacy MPharm or PhD, with preferably specialization in Regulatory Affairs or Pharmaceutics.

KLM Laboratories, our mission is to improve the lives of people around the world through innovative skincare/healthcare solutions

M.Pharm, B.Pharm, M.Sc ; Create new markets and clients in international business, drive sustainable business growth, manage product registrations, and follow up on orders and collections. Implement sales targets, plan budgets, and maintain strong client relationships and records.

Drafting and formatting product labels, packaging inserts, cartons, and leaflets according to regulatory and corporate guidelines.

Developing India-specific Artwork, Support to Regulatory dossier preparation and submissions like New drug applications, Site registration, Clinical trials and Import licence. Managing Registration samples right from dispatch of samples till the report.

B. Pharma / M.Pharma. Review and submission of injectable product dossiers for TGA and Europe in CTD, ACTD formats.

B.Pharm / M.Pharm. Regulatory Affairs Assistant Manager Europe Market. regulatory pathways for EU submissions and can compile EU eCTD dossier

Post graduate in Pharmacology or Regulatory science or a related field. experience in regulatory science, product development, clinical trials, or related fields.

Experience in Regulatory Affairs, CMC, Manufacturing, Quality Assurance/Control, Process Development, or Analytical Development in the pharmaceutical or biotechnology industry