Arslan Ahmed
Post-Marketing Surveillance Associate | Medical Devices | WIPRO
- Role
- Post Marketing Surveillance Associate - Medical Devices at Wipro
- Location
- Pune, MH, IN
- LinkedIn followers
- 500 followers
About Arslan Ahmed
I’m a B.Pharm graduate, graduated from Institute of Technology and Management, GIDA, Gorakhpur, in June 2025, with a passion for advancing healthcare through pharmaceutical innovation. My academic journey in pharmacology, pharmaceutics, biostatistics, and social pharmacy has equipped me with a strong foundation in drug development and quality assurance.In 2024, I completed a 45 days industrial training at Innovant Pharma Pvt. Ltd, gaining hands-on experience in tablet and capsule manufacturing and Quality Assurance, mastering Good Manufacturing Practices (GMP) and quality control protocols. My 3-month hospital training at PHC Zafra Bazar, Gorakhpur, further honed my skills in pharmaceutical care, patient counseling, and inventory management, bridging clinical and industrial perspectives.I thrive on analytical challenges and I am committed to ensuring safe, high-quality medicines. Academic projects in biostatistics and pharmaceutical marketing have sharpened my problem-solving and regulatory compliance skills. As an enthusiastic job seeker, I’m eager to join dynamic organizations in quality assurance or production roles, where I can contribute to patient well-being and grow as a professional.I’m always open to connecting with industry professionals, learning about new opportunities, and exploring certifications to enhance my expertise.Let’s connect to discuss how I can bring my skills and passion to the pharmaceutical world!
Experience
Post Marketing Surveillance Associate - Medical Devices
Jan 2026 — Present · Pune, IN
Associate – Post Market Surveillance (Medical Devices)| WiproWorking in the Healthcare & Life Sciences domain, focusing on post-market surveillance of medical devices. Responsible for reviewing and processing customer complaints, adverse event reports, and safety data to ensure regulatory compliance and patient safety. Supporting quality assurance, documentation, and reporting processes in line with global regulatory standards.Key Responsibilities:1. Processing and analyzing medical device complaints and safety reports2. Supporting adverse event reporting and regulatory documentation3. Ensuring compliance with global safety and quality standards4. Maintaining accurate case records and safety databases5. Collaborating with cross-functional teams to improve product safety6. Contributing to patient safety and risk management initiatives
Education
Dr. A.P.J. Abdul Kalam Technical University (AKTU), Lucknow
Bachelor of Pharmacy - B.Pharm, Pharmacy
Kendriya Vidyalaya
12th, Science
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