Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead regulatory affairs, manage submissions, and coordinate with global teams.
- Company: Join Reddy’s Laboratories, a top multinational pharma company dedicated to affordable healthcare.
- Benefits: Enjoy a dynamic work environment with opportunities for growth and innovation.
- Why this job: Make a real impact on global health while working with cutting-edge pharmaceutical solutions.
- Qualifications: Must have a degree in Pharmaceutical or Life Sciences and 3+ years in EU Regulatory Affairs.
- Other info: Fluency in English and digital skills are essential; project management experience is a plus.
The predicted salary is between 54000 - 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
Senior Manager/Director of Regulatory Affairs employer: Dr. Reddy's Laboratories
Contact Detail:
Dr. Reddy's Laboratories Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager/Director of Regulatory Affairs
✨Tip Number 1
Make sure to highlight your experience in EU Regulatory Affairs during networking events or industry conferences. Engaging with professionals in the field can lead to valuable connections and insights about potential job openings.
✨Tip Number 2
Stay updated on the latest regulatory changes and trends in the pharmaceutical industry. This knowledge will not only help you in interviews but also demonstrate your commitment to the field.
✨Tip Number 3
Consider joining professional organizations related to regulatory affairs. These groups often provide resources, job boards, and networking opportunities that can be beneficial in your job search.
✨Tip Number 4
Leverage LinkedIn to connect with current employees at Reddy’s Laboratories. Engaging with them can give you insider information about the company culture and the specific skills they value in candidates.
We think you need these skills to ace Senior Manager/Director of Regulatory Affairs
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Senior Manager/Director of Regulatory Affairs 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 maintain communication with various stakeholders.
Showcase Your Skills: Mention your proficiency in MS Office and any regulatory affairs software you are familiar with, such as AMS or RIMS. Highlight your digital savviness and how it can benefit the role.
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 Reddy’s mission and values.
How to prepare for a job interview at Dr. Reddy's Laboratories
✨Show Your Regulatory Expertise
Make sure to highlight your experience in EU Regulatory Affairs. Be prepared to discuss specific projects you've managed and how you navigated the complexities of regulatory submissions.
✨Demonstrate Communication Skills
Since fluent English is mandatory, practice articulating your thoughts clearly and concisely. Prepare examples of how you've effectively communicated with regulatory authorities and internal teams.
✨Highlight Project Management Experience
If you have project management experience, be ready to share how you've led projects in the past. Discuss your approach to coordinating with various stakeholders and ensuring compliance with regulations.
✨Be Digital Savvy
Familiarize yourself with relevant software like AMS, RIMS, and XEVMPD/IDMP. Be prepared to discuss how you've used these tools in your previous roles to enhance efficiency in regulatory processes.
