RAQA Specialist at Intuitive

Taipei, , Taiwan -

Full Time

Start Date

Immediate

Expiry Date

17 Dec, 25

Salary

0.0

Posted On

18 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Requirements, Medical Device Regulations, Product Registration, Regulatory Strategy, Communication Skills, Interpersonal Skills, Strategic Thinking, Quality Management System, Regulatory Intelligence, Post-Market Surveillance, Audit Participation, Technical Documentation, SAP, Veeva-RIM, Chinese Language, English Language

Industry

Medical Equipment Manufacturing

Description

Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere. We strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Passionate people who want to make a difference drive our culture. Our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of minimally invasive care. Job Description Product registration Understand regulatory requirements and medical device regulations. Spearhead all procedures of product registration, amendment, and administrative work precisely and efficiently, including planning, compiling registration submission, filing documents related and data archiving, reports, etc. Provide input on the product registration status and results to function head as well as stakeholders within ISI & IST to help their planning and business of the company. Assess the product changes and develop regulatory strategy to implement the change on time. Obtaining regulatory approval for new products, renewal, and amendment on time. Reporting the information to government according to relevant Taiwan Medical Device regulations. Manage SAP, Veeva-RIM regulatory database. Validate the content of approved labeling to ensure compliance with the relevant local Act and regulations for local labeling. Closely communicate with regulatory agencies and global counterparts to seek resolutions on regulatory issues. Ensures adherence to standard operating procedures and working instructions for the rapid and timely approval of new medical devices and regulatory support of marketed products. Provide RA input for cross-functional projects, including but not limited to the clinical trial, market access, etc. Actively participate in various RA&QA projects internally and externally. Participate in continuous training programs held by TFDA. Training hours and categories shall be taken in accordance with Regulations for Management of Medical Devices Technicians. Regulatory intelligence & surveillance Work closely with industry associations to build advocacy for Intuitive. Provide input to the global Regulatory Standard team on the local regulatory environmental changes to evaluate the impact and implement the necessary action in a timely manner. Review the promotional materials to ensure the compliance to local medical devices regulations and internal guidelines. QMS management Participate in internal and external audits as an auditee for regulatory affairs. Implement post audit activities and CAPA follow-up & closure for regulatory affairs related matters. Qualifications Required Skills and Experience Knowledge of Taiwan medical device act & regulations, ISO13485. Preferred >3 years of relevant RA experience in the medical device industry. Proven ability to review and translate technical documentation into effective regulatory submissions. Strategic thinking skill. Passionate and a great sense of responsibility. Good communication & interpersonal skill to work well with cross-functional teams. Excellent written and verbal communication skills in both Chinese and English command. Required Education and Training Bachelor’s degree in science, engineering, medical technology, life sciences or similar is required. Completed at least 20 hours of education and training in the past five years on the following topics: Domestic laws and regulations related to medical devices. Quality management system related to medical device manufacturing. Document preparation and process management for registration and market approval. Submission for registration and market approval. Post-market surveillance of medical devices. Working Conditions None Preferred Skills and Experience Experience in Agile Additional Information Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws. We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

Responsibilities

The RAQA Specialist will spearhead product registration procedures, ensuring compliance with regulatory requirements and medical device regulations. They will also manage communication with regulatory agencies and provide regulatory input for cross-functional projects.