WELLCURE REMEDIES
Website:
wellcureremedies.in
Job details:
Company Description WELLCURE REMEDIES, founded in 2002 in Andhra Pradesh, is a pharmaceutical and surgical products company focused on delivering high-quality, affordable healthcare solutions. The organization offers a wide range of anti-allergic, diabetic, and cardiovascular drugs in various dosage forms manufactured in line with WHO GMP guidelines. Products are supplied to hospitals and healthcare centers across India and exported to markets worldwide, with an emphasis on competitive pricing and timely delivery. WELLCURE REMEDIES leverages global sourcing and the reach of the internet to make quality healthcare products accessible to patients and customers in India and abroad. The company is committed to meeting urgent and bulk requirements while maintaining high standards of quality and customer service.
Role Description The Regulatory Analyst role is a full-time remote position responsible for supporting regulatory compliance across WELLCURE REMEDIES’ pharmaceutical and surgical product portfolio. Day-to-day activities include monitoring applicable regulations and guidelines, interpreting regulatory requirements, and assisting in the preparation and submission of regulatory reports and documentation. The Regulatory Analyst will collaborate with internal teams to ensure products and processes align with national and international standards, including WHO GMP and other relevant regulatory frameworks. This role also involves maintaining regulatory records, tracking deadlines, and helping prepare responses to regulatory authorities, audits, and inspections. The position requires proactive communication, attention to detail, and the ability to work independently in a remote setting while coordinating with cross-functional stakeholders.
Qualifications
- Strong knowledge of regulatory frameworks, including Regulations and Regulatory Requirements applicable to pharmaceutical and medical products.
- Experience with Regulatory Reporting and Regulatory Compliance processes, including preparation and review of regulatory submissions and documentation.
- Demonstrated Analytical Skills for interpreting guidelines, assessing risk, and supporting data-driven regulatory decisions.
- Familiarity with healthcare, pharmaceutical, or medical device industries and an understanding of quality standards such as WHO GMP or equivalent.
- Bachelor’s degree in Pharmacy, Life Sciences, Regulatory Affairs, or a related field; advanced certification in regulatory affairs is an asset.
- Strong written and verbal communication skills, with the ability to present complex regulatory information clearly and concisely.
- Proficiency in using digital tools for document management, data analysis, and remote collaboration.
- Ability to work independently, manage multiple deadlines, and maintain high accuracy and attention to detail in a remote environment.
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