Regulatory Affairs Assistant

Responsibilities:-To fully assist in product (medical device) registration and regulatory compliance with relevant government bodies for group of companies-To assist in implementation of ISO and GDPMD standard for group of companies-To assist in all administration jobs related to the regulatory affairs and quality assurance matters-Lead product registration,...

Responsibilities:-To fully assist in product (medical device) registration and regulatory compliance with relevant government bodies for group of companies-To assist in implementation of ISO and GDPMD standard for group of companies-To assist in all administration jobs related to the regulatory affairs and quality assurance matters-Lead product registration,...

**Job Summary**: The Regulatory Affairs and Quality Control Executive plays a crucial role in supporting the Regulatory Affairs and Quality Control Manager in ensuring compliance with regulatory standards and maintaining high-quality product standards. This position involves active participation in product registration activities, quality control processes,...

**REGULATORY AFFAIRS EXECUTIVE** *** The Regulatory Executive manages product and company license renewals with government agencies and ensures compliance with local laws and regulations. The role also monitors regulatory changes and updates management to prevent business risks. **RESPONSIBILITIES** **1. Regulatory Affairs & Compliance** - Prepare,...

**Key Responsibilities**: **1. Regulatory services & Pharmacovigilance & handling of controlled drug** - Review and approve marketing and promotion materials. Handle registration and maintain database of sales and advertisement permits issued by relevant authority bodies. - Responsible for the Regulatory Affairs (RA) functions and team members. - Provide...

**Requirements**: - Bachelor's degree in Quality Management or a related field - Minimum 2 years of experience in regulatory affairs, preferably in the medical device. - Strong attention to detail and ability to work under pressure to meet tight deadlines. - Excellent communication, organizational and project management skills. - Proficiency in regulatory...

About usNovugen is a wholly owned subsidiary of SciTech International, a UAE-based group with over 30 years of experience in the healthcare industry. We specialize in venturing into strategic healthcare businesses and developing world-class healthcare facilities across the globe. With operations in multiple countries across continents, our global presence...

To prepare compilation of pharmaceutical product dossier submission to NPRA and follow through with subsequent correspondence until approval to formalize changes requiring regulatory submission initiated in the company. - To be the person in charge/coordinator for variation related activities in the department. Responsible to ensure full adherence to...

Location : Seksyen U1, Shah Alam Salary : RM 3,500 - 5,500 **Key** Responsibilities**: - Responsible for the regulatory and compliance requirements for the products under the group of companies. - Ensure regulatory compliance by proactively monitoring, interpreting, implementing and conveying global and regional regulations that impact products and local...

Join Clinigen as a Medical Affairs Intern and gain invaluable hands-on experience within the dynamic field of pharmaceutical medical affairs. You will work closely with our experienced team to support our mission of delivering the right medicine to the right patient at the right time. This internship will provide you with exposure to various aspects of...