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- Tasks: Lead compliance efforts and manage regulatory submissions for innovative medicines.
- Company: Join Reddy’s, a global leader in affordable pharmaceuticals with over 24,000 passionate employees.
- Benefits: Enjoy a dynamic work environment with opportunities for growth and collaboration across global teams.
- Why this job: Make a real impact on healthcare access while working in a supportive and innovative culture.
- Qualifications: Must have a degree in Pharmaceutical Sciences or related fields and 3+ years in EU Regulatory Affairs.
- Other info: Fluency in English is essential; project management experience is a plus.
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
Compliance 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 Compliance Manager/Senior Manager
✨Tip Number 1
Familiarize yourself with the specific regulatory frameworks and guidelines relevant to the UK market. Understanding the nuances of UK MAA procedures will give you an edge in discussions and interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical regulatory affairs field. Attend industry conferences or webinars to connect with potential colleagues and learn about current trends and challenges in compliance management.
✨Tip Number 3
Showcase your project management skills by discussing specific projects you've led or contributed to in your previous roles. Highlighting your ability to manage timelines and coordinate with various teams will be crucial.
✨Tip Number 4
Demonstrate your digital savviness by being prepared to discuss your experience with RA-related software. Familiarity with tools like AMS, RIMS, and XEVMPD/IDMP can set you apart from other candidates.
We think you need these skills to ace Compliance Manager/Senior Manager
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Compliance Manager/Senior Manager position at Reddy’s Laboratories. Understand the key responsibilities and required qualifications, especially in EU Regulatory Affairs.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in EU Regulatory Affairs and any project management skills you possess. Be specific about your previous roles and how they relate to the responsibilities outlined in the job description.
Showcase Your Skills: Demonstrate your digital savviness by mentioning your proficiency with MS Office and any RA-related software you have used. Provide examples of how these skills have helped you in your previous positions.
Craft a Strong Cover Letter: Write a compelling cover letter that not only summarizes your qualifications but also expresses your passion for the pharmaceutical industry and your commitment to improving access to medicines. Make sure to align your values with Reddy’s mission: 'Good Health Can’t Wait.'
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. Be prepared to discuss specific regulations and how they apply to the pharmaceutical industry, as this will demonstrate your expertise and understanding of the role.
✨Highlight Your Project Management Skills
Since experience in project management is beneficial for this position, be ready to share examples of past projects you've managed. Discuss your approach to coordinating tasks, meeting deadlines, and collaborating with different teams.
✨Demonstrate Digital Savviness
Familiarize yourself with relevant software like AMS, RIMS, and XEVMPD/IDMP. During the interview, mention any experience you have with these tools and how you've used them to streamline processes or improve efficiency.
✨Prepare for Communication Scenarios
As communication with various stakeholders is key, think of examples where you've effectively communicated complex information to different audiences. This could include interactions with regulatory authorities or cross-functional teams.
