Dynamic and efficient "Global Regulatory & Compliance Professional" proficient in generic: API, Finished Formulations, Veterinary, Biologicals and Cosmetics
Key attributes: problem solving abilities, proactive mindset, goal and career oriented with a hunger to grow.
QUALIFICATIONS: M.Pharm (Pharmaceutics/Industrial Pharmacy/ Regulatory Affairs)
Industry experience:
1. 1-2 years in a Pharma Regulatory /Life Science company; 2. Hands on experience in filing application for the registration and import of generic from CDSCO in India. Experience in Co-ordination with IPC, CDTL, NIB and IVRI.
Job Profile: Provide regulatory and compliance support for India Market Post approval license maintenance during lifecycle management
Deliverables:
1. Regulatory classification and filing strategy aligned to domestic guidelines 2. Dossier Management & Technical Writing of regulatory documents 3. Agency Liaison for negotiation & pragmatic approvals
* Work hours: 9.30am-6.30pm, 5 days a week *Compensation package aligned to industry standards
If you think you are a fit or match reach out to us on: Email: cv@pharmaleaf.com
