Ra Specialist

Johnson & Johnson is currently seeking a RA Specialist located in Singapore. Position Summary As an APJ Veeva Coordinator, primary responsibility is to ensure the smooth operation and effective use of the Veeva system within the organization. The Veeva system is a copy clearance approval system for advertisement and promotional material, and local...

Job Highlight Location : Tuas Crescent MRT Salary: Up to S$3,200 + Variable Bonus Working Hours: 7.45 a.m. – 4.45 p.m. (Monday – Friday) About the Role Our client is looking for a motivated QA/RA Specialist to join our team. In this role, you will support Quality Assurance and Regulatory Affairs functions, ensuring compliance with ISO13485,...

Job Highlight Location : Tuas Crescent MRT Salary: Up to S$3,200 + Variable Bonus Working Hours: 7.45 a.m. – 4.45 p.m. (Monday – Friday) About the Role Our client is looking for a motivated QA/RA Specialist to join our team. In this role, you will support Quality Assurance and Regulatory Affairs functions, ensuring compliance with ISO13485, cGMP, and...

Roles & ResponsibilitiesJob HighlightLocation : Tuas Crescent MRT Salary: Up to S$3,200 + Variable Bonus Working Hours: 7.45 a.m. – 4.45 p.m. (Monday – Friday)About the RoleOur client is looking for a motivated QA/RA Specialist to join our team. In this role, you will support Quality Assurance and Regulatory Affairs functions, ensuring compliance with...

**Location** - Singapore, West**Job Type** - Permanent**Salary** - $3,500 - $8,000 Per Month**Date Posted** - 59 minutes agoAdditional Details **Job ID** - 97191**Job Views** - 6Roles & Responsibilities We are a global leader in the manufacturing of medical devices and delivering solutions to improve lives through today’s technology and future...

Singapore/Pharmaceutical Division **Job Purpose** To contribute as an integral member of Client’s Singapore RA team to support all regulatory activities for Client’s products. This includes the development and implementation of regulatory strategies, including the review, preparation of submissions, required to secure regulatory approval across various...

Join to apply for the Senior Specialist, RA & QA role at Vantive 18 hours ago Be among the first 25 applicants Join to apply for the Senior Specialist, RA & QA role at Vantive Get AI-powered advice on this job and more exclusive features. Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care...

Support the commercial organization and dealers/partners in ASEAN/South Asia to ensure their timely new product launches and sustainable registrations success. Manage communications and documentation between Business Units, distributors, regional head office and divisional RA, and manufacturing. - Ensure that regulatory activities are aligned with commercial...

Join to apply for the Senior Specialist, RA & QA role at Vantive 18 hours ago Be among the first 25 applicants Join to apply for the Senior Specialist, RA & QA role at Vantive Get AI-powered advice on this job and more exclusive features. Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care...

**Job Overview:**This is an exciting opportunity to support Quality Assurance and Regulatory Affairs functions, ensuring compliance with international regulatory requirements.The successful candidate will play a key part in product registrations, audits, and maintaining our company's Quality Management System (QMS).Key Responsibilities:Quality Assurance...