Headline

Associate | Pharmacovigilance & Drug Safety Enthusiast | Clinical Data Management | B.Pharm | Content Management | Research Writing & Analytics

About

I am a results-driven professional currently working as an Associate at Suavis India Software Services, specializing in content management and digital communication using WordPress. My work involves creating, organizing, and optimizing digital content to enhance accessibility and user engagement. With a Bachelor of Pharmacy (B.Pharm) from Rajmata Jijau Shikshan Prasarak Mandal’s College of Pharmacy, I bring a strong foundation in pharmaceutical sciences, pharmacology, and regulatory principles. This scientific background complements my expertise in content strategy, data organization, and written communication. My goal is to contribute to drug safety and clinical research through data accuracy, regulatory compliance, and scientific communication. I’m actively seeking opportunities as a Drug Safety Associate, PV Assistant, or Clinical Data Analyst where I can apply analytical thinking and scientific precision to improve patient safety.

Location

Pune District

Work experience

Associate at Suavis India Software Services Pvt Ltd, Jul 2023 - Present · 3 yrs, Pune District, Maharashtra, India, Manage end-to-end content creation, organization, and publishing using WordPress CMS. Ensure consistent content quality, accuracy, and accessibility across digital platforms. Utilize categories, tags, and navigation tools to improve user experience and SEO visibility. Collaborate with cross-functional teams to align digital assets with organizational goals. Developed strong skills in written communication, version control, and content optimization.

Industrial Training at NuLife Pharmaceuticals, Nov 2023 - Nov 2023 · 1 mo, Pune/Pimpri-Chinchwad Area, During my one-month industrial training at Nulife Pharmaceuticals Pvt. Ltd., I gained hands-on exposure to various stages of pharmaceutical manufacturing, quality control, and documentation processes. The training provided practical insights into Good Manufacturing Practices (GMP), quality assurance protocols, and regulatory compliance standards followed in the pharmaceutical industry. Key Learnings and Responsibilities: Observed and understood formulation, blending, granulation, compression, and coating processes in tablet manufacturing. Learned about Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), and in-process quality checks. Assisted the QA team in reviewing documentation for compliance with WHO-GMP and Schedule M guidelines. Gained understanding of Quality Control testing, including sampling, assay, and stability studies. Understood the workflow between Production, Quality Assurance, and Regulatory Affairs departments. Developed awareness of safety procedures, equipment handling, and cleanroom practices.

Education

Bachelor of Pharmacy - BPharm, Pharmaceutical Sciences, Rajmata Jijau Shikshan Prasarak Mandal's College of Pharmacy, Dudulgaon, Pune 412105

Bachelor of Arts - BA, English and History, Yashwantrao Chavan Maharashtra Open University