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- Tasks: Lead regulatory submissions and maintain communication with authorities and partners.
- Company: Join Reddy’s, a global leader in affordable and innovative pharmaceuticals.
- Benefits: Enjoy a collaborative culture and the chance to make a real impact on health.
- Why this job: Be part of a mission-driven team that accelerates access to essential medicines.
- Qualifications: Degree in Pharmaceutical or Life Sciences with 3+ years in EU Regulatory Affairs required.
- Other info: Fluency in English and digital skills are essential for success.
The predicted salary is between 48000 - 84000 ÂŁ per year.
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
Regulatory Affairs Manager /Senior Manager employer: Dr. Reddy's Laboratories
Contact Detail:
Dr. Reddy's Laboratories Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager /Senior Manager
✨Tip Number 1
Make sure to familiarize yourself with the specific regulatory frameworks and procedures in the UK, as well as the European Union. Understanding the nuances of MAA procedures will give you a significant edge during discussions with potential employers.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those working in regulatory affairs. Attend industry conferences or webinars to connect with key players and learn about the latest trends and challenges in the field.
✨Tip Number 3
Highlight your project management skills during interviews. Being able to demonstrate your ability to manage multiple regulatory projects simultaneously can set you apart from other candidates.
✨Tip Number 4
Stay updated on digital tools and software relevant to regulatory affairs. Familiarity with platforms like AMS, RIMS, and XEVMPD/IDMP can showcase your digital savviness and readiness to adapt to the technological demands of the role.
We think you need these skills to ace Regulatory Affairs Manager /Senior Manager
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Regulatory Affairs Manager position at Reddy’s Laboratories. Understand the key responsibilities and required qualifications to tailor your application accordingly.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in EU Regulatory Affairs and any project management skills you possess. Use specific examples that demonstrate your ability to handle regulatory submissions and communication with authorities.
Showcase Your Skills: Mention your proficiency in MS Office and any regulatory affairs software you are familiar with, such as AMS or RIMS. Highlighting your digital savviness can set you apart from other candidates.
Craft a Compelling Cover Letter: Write a personalized cover letter that reflects your passion for the pharmaceutical industry and your commitment to accelerating access to affordable medicines. Make sure to connect your background and skills to the mission of Reddy’s Laboratories.
How to prepare for a job interview at Dr. Reddy's Laboratories
✨Show Your Regulatory Knowledge
Make sure to brush up on your knowledge of EU regulatory affairs, especially regarding MAA procedures. Be prepared to discuss specific regulations and how they apply to the role.
✨Demonstrate Project Management Skills
Since experience in project management is beneficial, be ready to share examples of projects you've managed. Highlight your ability to coordinate with various teams and meet deadlines.
✨Communicate Effectively
Fluency in English is mandatory, so practice articulating your thoughts clearly. Be prepared to explain complex regulatory concepts in a way that is easy to understand for non-experts.
✨Be Digital Savvy
Familiarize yourself with relevant software like AMS, RIMS, and XEVMPD/IDMP. During the interview, mention any experience you have with these tools and how they can enhance regulatory processes.
