Senior Manager/Director Of Regulatory Affairs

Reddy's Laboratories Ltd. ("Reddy's") is a leading multinational pharmaceutical company based across global locations.
Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can't Wait .

Module 1 and the national texts), submission, coordination and monitoring of UK (national, IRP) MAA procedures
Maintenance and communication with internal and external contacts and interfaces, e.g.
regulatory authorities, European affiliates, Headquarter and partners/customers (e.g.
Other regulatory related activities including but not limited to:
# Dealing with PIL and SmPC uploads and maintenance on eMC website
# Review and approval of UK packaging materials artworks and maintenance proper archive
# Assist in obtaining Certificates of a Pharmaceutical Product and notarization/legalization of these where required
# Provision of advice and/or information to teams such as the Quality, Marketing and Medical Information teams.

Study / Degree in Pharmaceutical Sciences, Life Sciences or Natural Sciences with at least three year experience in EU Regulatory Affairs incl.
Fluent in English is mandatory as it is used as the main communication language
Experience in project management is beneficial
Digital Savvy, with good knowledge of MS Office and RA related software like AMS, RIMS, XEVMPD/ IDMP