Ra Specialist

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 & Responsibilities 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...

Job Description:Support our Quality Assurance and Regulatory Affairs functions as a QA/RA Specialist.Ensure compliance with ISO13485, cGMP, and international regulatory requirements.Play a key role in product registrations, audits, and maintaining the company's Quality Management System (QMS).Key Responsibilities:Quality Assurance (QA)Implement and maintain...

Job Description: Support our Quality Assurance and Regulatory Affairs functions as a QA/RA Specialist. Ensure compliance with ISO13485, cGMP, and international regulatory requirements. Play a key role in product registrations, audits, and maintaining the company's Quality Management System (QMS). Key Responsibilities: Quality Assurance (QA) ...

Job Description: Support our Quality Assurance and Regulatory Affairs functions as a QA/RA Specialist. Ensure compliance with ISO13485, cGMP, and international regulatory requirements. Play a key role in product registrations, audits, and maintaining the company's Quality Management System (QMS). Key Responsibilities: Quality Assurance (QA) ...

Singapore/Pharmaceutical Division (12-mth contract) **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...

I am currently representing a **medical device company **headquartered in **US **with a specialistation of **high risk medical devices **in **Orthopaedics **. They are currently seeking a **Senior RA Specialist, APAC **to join their brilliant and ambitious team, to propel their regulatory activities in the region. This successful incumbent will be focusing...

Overview: **FUNCTION/DEPARTMENT: INTELLECTUAL PROPERTY AND REGULATORY AFFAIRS (IPRA)** **REPORTING TO: IPRA MANAGER/ASSOCIATE MANAGER** **DIRECT REPORTS: NIL** **Responsibilities**: **RESPONSIBILITIES**: - Manages regulatory projects registrations, including preparation of registration dossier, submission and follow up with regulatory authorities -...

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,...

Responsibilities**:RA** - Audit & Inspections - Participates in regulatory agency inspections as needed and assists in dispersing the information as appropriate - Prepares, files, and submits responses to external quality surveys, tender and questionnaires - Manufacturing site - Support and perform regulatory risk assessment for CAPA, QN deviations,...