Hospira is the world’s leading provider of injectable drugs and infusion technologies. Through our broad, integrated portfolio, we are uniquely positioned to Advance Wellness™ by improving patient and caregiver safety while reducing healthcare costs.
Job Title – Regulatory Affairs Professional – all Levels
Experience – 5 – 10 years.
Location – Chennai, Visakhapatnam/Vizag
Job Description:
Suitable candidates for listed roles can Walk-In for the interview:
- Life Cycle Management & Post Approval Changes (US& EU, all Dosage Forms)
- Regulatory Conformance / Dossier Management
- Manufacturing Site Support
- Global Labelling Management (CDS, CSI, SMPC and USPI)
API RA / DMFs - Biosimilars RA (US&EU)
- Submision Management / Regulatory Operations
- Regulatory Strategists / Authors (Sterile Injectables)
- Database Management & Archival
Eligibility Criteria:
- Candidates with 3 to 15 years of Pharma or Biotech experience in RA function for major Markets like US, Europe, Canada, ROW Regions;
- Should be Excellent in: Communication Skills; Regulatory Knowledge; Project Management Skills;
- Computer Knowledge; Eye for Details & Reasoning
Skills.
Desired Profile:
- UG -B.Pharma – Pharmacy, B.Sc
- PG – M.Pharma, M.Sc
Walk-In Details:
- Date of Interview – 21st January – 22nd January 2017
- Time of Interview – From 09:00 AM
- Venue of Interview – Gurgaon On 21st & 22nd Jan, 2017, Crowne Plaza Today Gurgaon, Sector 29, National Highway-8, Gurgaon 122001 New Delhi(NCR)
