Regulatory Medical Intern

**Regulatory Affairs Specialist**: - Remote Eligible: Hybrid- Onsite Location(s): Jakarta, IDWe are seeking a Regulatory Affairs Specialist for our Indonesia Team. He/she ensures rapid and timely approvals for respective product lines by plans on all product registration, manage all product registrations' preparation and documentation. He/she Interacts with...

COMPANY DESCRIPTION **Listed on the Catalist board of the Singapore Exchange (SGX), Hyphens Group has a direct presence in Singapore (HQ), Vietnam, Malaysia, Indonesia and the Philippines, and is supplemented by a marketing and distribution network covering additional jurisdictions like Hong Kong, Myanmar, Brunei, Cambodia, Oman, Bangladesh, South Korea and...

Responsible for managing and submitting regulatory filing materials, communicating with government departments, and handling matters related to regulatory filing strategies. - Ensure compliance with local, national, and international regulatory requirements for company products, and develop **Corporate Regulatory Manuals & Guidelines** as company standards...

Aspen Medical seeks expressions of interest in Site Emergency Physician for an upcoming opportunity for occupational and industrial health services. **Locations**: PNG, Fiji, Indonesia, Vanuatu, Malaysia, Vietnam, Philippines, Kiribati **Responsibilities may include; but not limited to**: - Provide general administrative support including management of...

With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the leading company solely dedicated to skin and advancing the future of dermatology. We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all,...

PT. Merhati Keluarga Medika is a healthcare company that focuses in innovative pharmaceutical and medical device products. We are now seeking a _**Regulatory Affairs Officer & PJT **_as the team continues to grow and develop into its next phase. **I. Qualifications & Requirements** - At least 2 (two) years of relevant experience in regulatory affairs in a...

The regulatory & labeling compliance specialist will ensure that only registered/licensed products are allowed for shipment to respective regulated APAC countries from the Molecular Diagnostics (MDx) Regional Distribution Centre in Singapore. In addition, the specialist is also responsible for ensuring compliant country specific addendum labeling are...

You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind,...

**Summary**: In line with overall product strategy, the Medical Lead is responsible for supporting the design, implementation and execution of Medical Affairs plans for assigned Therapy Area, providing scientific information, helping design & organise clinical studies, building educational dialogue with KOLs and regulatory stakeholders This role will help...

Johnson & Johnson is recruiting a Regulatory Affairs Specialist based in Indonesia The Regulatory Affairs Specialist, Medical Device, Indonesia, is a member of the local Regulatory Affairs department, responsible for actively contributing to the regulatory compliance of medical devices under their responsibility. The position is responsible for providing...

10+ years of regulatory affairs experience in the pharmaceutical and medical devices industry **Prior experience preparing and reviewing submissions to BPOM** - Experience in Submission of New Drug Applications, Generic Drug Applications, Medical Devices Registration - Experience in Post Marketing Maintenance, Lifecycle Management of Marketed Drugs and...

**Responsibilities**: - Develop tactics for communicating complex medical and scientific information to the healthcare community, including support for answering unsolicited medical questions, adverse event reporting, and other clinically related medical information. - Acts as a strategic partner alongside Commercial and R&D, and medical and scientific...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. **A Day in the Life **:We are a learning culture. An inventive and collaborative group. We are dedicated to making...

Job Responsibilities: - Develop tactics for communicating complex medical and scientific information to the healthcare community, including support for answering unsolicited medical questions, adverse event reporting, and other clinically related medical information. - Acts as a strategic partner alongside Commercial and R&D, and medical and scientific...

Reviewing/ arranging/ submitting registration document for our** **products to BPOM. - Follow up registration status and coordination among departments within Kalbe group. Job requirement: - Min. GPA 3.00. - Having one year of working experience as Regulatory Officer/ Supervisor for pharmaceutical or medical devices is a plus. - Fresh graduates are welcome...

The Medical Science Liaison (MSL) functions as a highly trained, field-based, scientific expert who engages healthcare professionals to exchange clinical, scientific, and research knowledge. Following regulatory and corporate guidelines, they will facilitate and build scientific relationships and collaborations with the medical/scientific...

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office 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...

The SEA Regional Medical Advisor directs the operational function in medical affairs to achieve organizational objectives. Responsible for the design, development and implementation of programs related to educational, promotional and reporting materials for products related to Phase IIIb, Phase IV trials, solicited and non-solicited studies, publications,...

**Job Title: Oncology Medical Scientific Liaison** **Location: Jakarta, Indonesia** **About the role**: The Medical Science Liaison (MSL) establishes Takeda’s medical affairs presence with external stakeholders through scientific exchange and research support. This role is the field-based therapeutic area (TA) expert responsible for execution of the TA...

**Objective** The Medical Science Liaison (MSL) establishes Takeda’s medical affairs presence with external stakeholders through scientific exchange and research support. This role is the field-based therapeutic area (TA) expert responsible for execution of the TA specific medical plan in the field, predominantly by establishing, developing, and fostering...