QA / Ra Specialist (Medical Devices)

**THE OPPORTUNITY**: An esteemed **Medical Devices Company **is currently seeking a highly capable **Regulatory Affairs Specialist **to join their team. The successful incumbent will be tasked with the development and implementation of efficient regulatory strategies and processes, ensuring timely product registration, life cycle management, and post-market...

**Location** - Singapore, Central Singapore**Job Type** - Permanent**Salary** - $5,000 - $6,000 Per Month**Date Posted** - 3 hours agoAdditional Details **Job ID** - 98844**Job Views** - 1Roles & Responsibilities Our client is a biotechnology company specializing in developing proprietary non-invasive medical devices. The company is certified to EN ISO...

**Job summary** Lead global QA & RA team. Provide sufficient QA & RA initiation and involvement while providing product or service to customers, ensure those products or service meet all applicable regulation requirements, customer expectation and company objectives. **Responsibilities** 1. Establish, maintain and improve Quasar global quality management...

Partnering with an esteemed **Medical Devices Company **, our client is seeking a **Regulatory Affairs Executive **to join their team. The successful incumbent will be responsible for developing and implementing effective regulatory strategies and processes to support the timely registration of new products, life cycle management and post-market...

**POSITION PURPOSE**: This individual is responsible for the processing all regulatory affairs matter related to the product life cycle from premarket to post market activities, advising the team on appropriate regulatory procedures to ensure products are legally marketed in the respective country. The incumbent is responsible to draft a regulatory...

My Client, a leading US Medical Device Company is looking out for a QA Specialist to support them in their recent expansionary plans in Singapore. The requirements and skills possessed by the incumbent are as such: **Job Responsibilities: - Support in supplier and internal audits within Singapore and support audits in APAC region ensuring effectiveness of...

**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...

Job Description - Develop and execute regulatory plans for complex projects including new products and maintenance of existing marketing authorizations - Represent or lead the RA function on assigned cross-functional project teams - Monitor applicable regulatory requirements; assure compliance with NDRMedTech and external standards - Establish appropriate...

**Location**: Singapore **Salary**: Open **Industry**: Healthcare & Life Sciences **Sub-industry**: Medical Devices **Function**: Healthcare R&D **Job Description**: **Our Client**: Our client is a Japanese Regional HQ that focuses on medical technology for infection control and laboratory uses. They manage the sales and marketing for the Asia-Pacific...

**Job Details**: **Location** Singapore **Salary** Competitive Salary **Job Type** Permanent **Ref** BH-19433 **Contact** Roselle Cuntapay- **Posted** about 2 hours ago - We are currently looking for a RA Specialist for a new entrant to the Singapore market that focuses on IVD products. You will be taking charge of everything Regulatory across the...

Our client is a MNC in the Medical Devices industry with a strong and expanding portfolio **Roles and Responsibilities** - Prepare and submit regulatory submissions, including product registrations, variations, and renewals, to regulatory authorities in APAC countries. - Develop and implement regulatory strategies to support the successful approval and...

EPM Scientific - Phaidon International is a leading multinational medical devices company seeking an experienced Medical Devices Training Specialist to join our team in Singapore.About Our Role:This role involves developing and delivering comprehensive training programs for clinical staff and customers. The successful candidate will have a strong background...

**Overall Responsibilities** The RAQA Specialist will be responsible for regulatory and quality projects and improvements to meet company goals. This includes ensuring compliance to Regulatory Affairs (RA), Quality Systems (QS) and Quality Assurance (QA) requirements in SEA markets for Applied Medical products by performing premarket and post-market...

**THE ROLE Representing a renowned Medical Device MNC with its regional office located in Singapore, this Company is seeking a Regional QA Associate Manager to join their team to manage their regional QA responsibilities. The Regional QA Associate Manager will be responsible for follow-up and maintenance of the Quality System processes, in compliance with...

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,...

We are seeking a skilled professional to join our team as a Medical Device Commercialization Specialist at SINGAPORE HEALTH SERVICES PTE LTD. In this role, you will be responsible for leading the commercialization efforts of our medical technologies, working closely with the incubator team to develop and implement strategies for success.

Job OverviewAll Things Medical Billing is a leading provider of medical devices and supplements dedicated to orthopedics. We are seeking a highly skilled sales professional to join our team in representing our company in the medical device industry.The successful candidate will be responsible for developing and executing strategic sales plans to achieve...

Job Purpose - Implement and lead development of programs that will support APJ Vision RA team digital transformation roadmap. - Partner with the regulatory affairs team as well as cross functional stakeholders to build and drive digital solutions that will support workflow and strategy optimization. - Responsible for the day-to-day processing and validation...

Job Purpose - Implement and lead development of programs that will support APJ Vision RA team digital transformation roadmap. - Partner with the regulatory affairs team as well as cross functional stakeholders to build and drive digital solutions that will support workflow and strategy optimization. - Responsible for the day-to-day processing and validation...

Olympus APAC is seeking a skilled Medical Device Service Specialist to join our team.Job Description:To maintain and improve the service education system for trainers and distributors in the Asia Pacific region.To conduct in-service training on medical devices and related products for trainers in other Business Centres and distributors, including repair...