Medreich Hiring for Pharmacovigilance Associate
Key Points:
| Position | Pharmacovigilance Associate (XEVMPD) |
|---|---|
| Organization | Medreich (A Meiji Group Company) |
| Location | Bangalore |
| Qualification Required | B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences |
| Experience | 1 to 4 Years |
| Salary | ₹25,000 – ₹35,000 per month |
| Skills & Competencies | xEVMPD knowledge, ICSR handling, analytical skills, attention to detail, problem-solving |
| How to Apply | Send CV to sekhar.s@medreich.com |
Exciting Career Opportunity as a Pharmacovigilance Associate at Medreich Pharmaceuticals
Are you ready to take your career in pharmacovigilance to the next level? Medreich Pharmaceuticals, part of the globally esteemed Meiji Group, is seeking skilled professionals for the role of Pharmacovigilance Associate (XEVMPD). This opportunity, based in Bangalore, allows you to contribute to global healthcare by ensuring the safety and efficacy of pharmaceutical products.
About Medreich Pharmaceuticals
With over four decades of experience, Medreich has built a solid reputation in the pharmaceutical industry. Known for its commitment to innovation and high-quality healthcare solutions, the company is a part of the Meiji Group, a global leader in healthcare and food products. Medreich focuses on providing superior pharmaceuticals, maintaining a legacy of excellence in manufacturing, research, and distribution.
As a Pharmacovigilance Associate, you’ll be joining a company that is dedicated to maintaining the highest safety standards for its drugs, protecting patient health and ensuring compliance with global regulations.
What the Role Involves
The Pharmacovigilance Associate position is designed for individuals who are passionate about drug safety and compliance. Your role will be critical in ensuring that all safety data related to Medreich’s products are captured, analyzed, and reported accurately. Some of your core responsibilities include:
- Handling ICSRs (Individual Case Safety Reports): You’ll be responsible for receiving and assessing EVWEB ICSRs, ensuring that the safety reports are handled efficiently and thoroughly analyzed for potential risks.
- Medical Literature Monitoring (EMA-MLM): You’ll conduct regular reviews of medical literature, particularly in compliance with European Medicines Agency (EMA) guidelines, to detect any relevant safety information for marketed products.
- Electronic Reaction Monitoring Report (eRMR): In this role, you will oversee eRMR analysis to identify any adverse drug reactions, ensuring that patient safety is prioritized at all times.
- Database Management (xEVMPD Activities): Maintaining and updating crucial pharmacovigilance databases, including QPPV, SmPC, and MAH information, will be one of your key tasks. This ensures that Medreich complies with all regulatory requirements regarding pharmacovigilance data.
Who Should Apply?
If you hold a degree in Pharmacy, Life Sciences, or related fields such as B.Pharm, M.Pharm, Pharm.D, M.Sc, or B.Sc, this could be the perfect role for you. Medreich is looking for professionals with 1 to 4 years of experience in pharmacovigilance or pharmaceutical safety operations. Additionally, familiarity with xEVMPD database management and global pharmacovigilance regulations is highly desirable for this role.
Desired Skills and Competencies
In addition to meeting the qualification and experience requirements, the ideal candidate should possess the following skills:
- Experience with xEVMPD: Knowledge of extended EudraVigilance Medicinal Product Dictionary (xEVMPD) operations is crucial. You’ll be responsible for maintaining and updating critical pharmacovigilance data in this database.
- Strong Analytical Skills: You need to be able to assess Individual Case Safety Reports (ICSRs) and identify any safety signals that may pose risks to patients.
- Attention to Detail: Accuracy is key in pharmacovigilance, and attention to detail ensures that all safety reports and databases are correctly maintained.
- Effective Communication: You should have excellent communication skills to report findings and update safety information within the company and to external regulatory bodies.
- Problem-Solving Abilities: This role requires proactive thinking, especially when it comes to managing safety data and ensuring compliance with regulatory standards.
Why Join Medreich Pharmaceuticals?
Medreich offers a fantastic opportunity for professionals to grow within the pharmacovigilance field. Not only will you be part of a renowned pharmaceutical company, but you’ll also get the chance to work in an environment that emphasizes innovation, operational excellence, and a commitment to patient safety. With a competitive salary range of ₹25,000 – ₹35,000 per month, this position offers an exciting career path for individuals passionate about drug safety.
How to Apply
If you meet the qualifications and are ready to contribute to Medreich’s mission of ensuring drug safety, send your updated CV to sekhar.s@medreich.com. Take this opportunity to make a significant impact in the pharmaceutical industry while advancing your career in pharmacovigilance!