Aculife has been associated with the healthcare segment since over last 30 years now, which is the prime reason why the name spells unparalleled growth and absolute reliability. It also enjoys a market leader position in one of the largest economies of the world. Aculife boasts of a customer-centric vision, and is committed to offer quality products and services that maximize value to its valued customers. Aculife is one of the world’s largest sterile manufacturing facility spread over 550 acres.
Position: Regulatory Affairs
Educational Qualification: M. Sc/M. Pharm/B. Sc/B. Pharm/Life Science
Experience needed: 0-01 Years in RA
Location: Ahmedabad
Job Description
Job Role:
1. CTD, ACTD, and ECTD dossiers must be prepared, compiled, and reviewed.
2. Handling customers and MOH inquiries about technical documentation (Stability Data, GMP, FSC, DMF, and so on).
3. A minimum of one year of experience in QA or an Analytical Development Lab is required.
Interested candidates can apply: mayurparmar@aculife.co.in sankitakhonde@aculife.co.in
 
 
