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An ISO 9001:2015 Certified Company

WORK FOR QUALITY

REGULATORY PROFESSIONAL

M. PHARMA (DRA)

  • Undertake regulatory submissions to DCGI

  • Compilation of application as per checklists

  • Coordinate with clients to resolve their queries and follow-up for on-going projects

  • Able to communicate with new leads and thrive to materialise them

  • Team up with technical experts in the office and solve challenges regarding Regulatory Affairs

Package: 

3 Lakhs p.a. (1-2 Years Experience)

1.80 Lakhs p.a. (Fresher)