Medreich Limited Hiring for Regulatory Affairs/ Microbiology- apply Now
Join Medreich Limited – Elevate Your Career in Pharmaceutical Excellence!
Since 1976, Medreich Limited has been a leading name in the pharmaceutical industry, recognized for its dedication to manufacturing high-quality generic and branded drugs across diverse therapeutic areas. With over 2,900 employees globally, we have established a formidable presence in 54 countries, constantly pushing the boundaries of innovation and product superiority. At Medreich, we strive to maintain exceptional standards of quality, ensuring that every product we develop and manufacture stands as a testament to our commitment to excellence.
As a part of our continuous expansion and commitment to delivering superior healthcare solutions, we are currently seeking talented professionals to join our dynamic Research & Development (R&D) team in Bengaluru. If you are passionate about advancing your career in the pharmaceutical industry, Medreich offers a unique opportunity to be part of an organization that not only values your skills but also fosters growth and innovation. We are hiring for the following key positions:
1. Executive – Microbiology
- Experience Required:Â 4 to 6 years
- Education:Â M.Sc. in Microbiology
In this role, you will be responsible for ensuring the integrity and quality of our microbiological processes and products. We are looking for individuals who possess in-depth expertise in microbiology, with experience in pharmaceutical environments being highly preferred. Your contributions will directly impact the safety and efficacy of our products, making this a vital role within our organization. If you have a keen eye for detail, a deep understanding of microbial testing, and a passion for maintaining the highest quality standards, this position is perfect for you.
2. Regulatory Affairs Professional
- Experience Required:Â 5 to 7 years
The Regulatory Affairs (RA) Professional position is critical to ensuring that our products meet the stringent standards of regulated markets. As part of the RA team, you will take on responsibilities such as:
💡 Technical Review and Dossier Compilation: You will manage the technical review and compilation of registration dossiers for submission to regulated markets. Your work will help ensure that our products adhere to all regulatory requirements, facilitating seamless approval processes.
💡 Master Document Review: You will review key documents, including Specifications, Master Formula Records (MFR), Batch Manufacturing Records (BMR), Batch Packing Records (BPR), Process Validation Protocols (PVP), Process Validation Reports (PVR), and many others. Your thorough and meticulous review of these documents will ensure compliance with industry standards.
💡 Deficiency Management: You will handle any deficiencies identified during the product registration process in regulated markets, ensuring that all issues are resolved promptly and accurately. Your work will be integral in navigating complex regulatory landscapes and ensuring that our products meet the highest international standards.
At Medreich, we believe that our people are our most valuable asset. That’s why we are committed to providing an environment that encourages continuous learning and professional development. In addition to competitive salaries and benefits, we offer the opportunity to work in a collaborative and innovative environment, where your contributions will make a real difference in the lives of patients around the world.
Why Medreich Limited?
Working at Medreich means being part of a company that has a long history of delivering excellence in pharmaceutical manufacturing. Our commitment to quality, safety, and innovation is at the heart of everything we do. By joining us, you will have the chance to work with some of the best minds in the industry and contribute to groundbreaking advancements in healthcare.
How to Apply
We are looking for talented individuals who are eager to make an impact in the pharmaceutical industry. If you believe you have the experience and passion to excel in either of these roles, we would love to hear from you!
- Location:Â Bengaluru (Bommasandra)
- Submit Your Resume:Â Please send your updated resume to [email protected] or [email protected].
Join us in our mission to improve healthcare worldwide, and be a part of a company that is constantly raising the bar in pharmaceutical excellence. Don’t miss this opportunity to advance your career with Medreich Limited. We look forward to welcoming you to our team!