Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

The Regulatory Affairs and Quality Supervisor (Lead) is responsible for execution of PT Indonesia quality assurance, registration policies and standards, and ensures the regulatory compliance to local and international regulations. The role will call for a strong strategic orientation in order to drive the right strategic decisions for quality pathways that will optimize the time to market and ensure on time registration and maintenance of operational licenses and government approvals.

 

What will you do?

 

The successful candidate will evaluate existing and future regulations, mentorship documents, and industry standards in Indonesia to resolve their influence on the business area in Indonesia. Work closely with both internal and external parties, as well as authorities, to expand the product portfolio and develop a regulatory plan that aligns with the vital legislation in Indonesia.

Pre-market registration/listing and post-market surveillance activities for IVD and medical device with the Ministry of Health and other government officialsEstablish and maintain certification to IDAK, CDAKB, and other regulatory standards, and RUO listing with MOHReview of dossier files before submission and collaborating with Global & Regional Regulatory teamReport to local authorities in a timely manner on post market surveillance activities (e.g., Adverse Event Reporting and Field Safety Corrective Action)Responsible for developing and implementing quality management systems in our Indonesian entityResponsible for the inspection and management (including training) of service providers to ensure they meet local regulations and quality standards for medical device and IVDDevelop and maintain the quality management system based on national regulatory standards.

 

How will you get here

 

Education:

Bachelor's degree in biomedical engineering, pharmacy, or equivalent field. Equivalent experience in a related field will also be considered

Experience:

5+ years of regulatory experience in either IVD and/or medical device industries.Good understanding in CDAKB requirements (Completed CDAKB training is an advantage)Proven experience in Project management in lead regulatoryInvolvement in industry associations will be an advantage (e.g., APACMed, GAKESLAB).Successful experience in communicating with regulatory agencies and customer facing experience

 

Knowledge, Skills, and Abilities

Must possess strong organizational skills and be able to prioritize multiple projects concurrentlyKnowledge of IVD/MD registration, RUO submission process in IndonesiaWorking experience in direct liaising with the authority and ability to respond optimally to authority queries.Proficient in both verbal and written communication skills in Indonesian and English and strong presentation skills.Strong interpersonal skills, able to remain calm, professional, respectful, and positiveWork as a team member in a fast-paced environment with limited supervisionSkilled at building strong connections with colleagues from departments in a collaborative work setting, as well as with partnersA collaborative individual who can also demonstrate the ability to work independentlyPositive attitude, proactive approach, and a willingness to learn

 

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. A one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

 

Apply today!

 

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.

 

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.