Hetero Drugs, a leading USFDA approved Pharmaceutical Company (One of the top 10 Indian pharmaceutical companies with global outreach), based at Hyderabad, Telangana is looking for experienced professionals for Quality Assurance & Regulatory affairs departments for our corporate office.
Quality Assurance – Executives to Managers: M.Sc. with Organic or Analytical chemistry having 4-10 years experience in API Bulk drug manufacturing Quality functions.
Regulatory Affairs (API) – Executives to Managers: M.Sc. with Organic or Analytical chemistry having 2-10 years experience in API Bulk drug manufacturing Regulatory affairs functions. Should have exposure in filing DMF in EU & US markets
Regulatory Affairs (Formulations) – Executives to Managers: M.Sc. or B.Pharma or M.Pharma having 2- 10 years experience in Formulations regulatory affairs functions. Should have exposure in filing Dossiers in EU, US, China, Middle East, Mexico & African markets.
Interested candidates may call on 9989619407 for Regulatory Affairs and 9849331536 for Quality Assurance to schedule an appointment for interview on 22-06-2014 (Sunday).
Venue: Hetero Drugs Limited
7-2-A2, Industrial Estates, Sanatnagar, Hyderabad
Candidates who are unable to attend the interviews can send their CVs to: firstname.lastname@example.org