Regulatory Affairs Specialist

**Mô tả công việc**: (Mức lương: Thỏa thuận) To manage registration and compliance matters for global brands according to Vietnam’s regulation. Principal Accountabilities Main responsibilities: - Manage the processes to notify DAV or to obtain regulatory approvals for new / existing products within the identified timeframes - Manage the...

Prudential’s purpose is to be partners for every life and protectors for every future. Our purpose encourages everything we do by creating a culture in which diversity is celebrated and inclusion assured, for our people, customers, and partners. We provide a platform for our people to do their best work and make an impact to the business, and we support...

**Mô tả công việc**: (Mức lương: Đến 14 triệu VNĐ) - Products registrations: submit new, renew and follow-up of all registration documents for all products: cosmetics, food supplements, medical devices and drugs. - Be proactive to suggest and find solutions when confronted to regulatory affairs issues - Collaborate with authorities in a smart...

**Location**:Ho Chi Minh, VN, VN**Job Function**:Client and Customer Services**Requisition Number**:143826**Description**: **Job Summary** - Manage and archive PV documents and RA/PV SOPs **General Responsibilities** **Pharmacovigilance** - Assume back-up role in the absence of PV main contact - Receive, follow up Safety reporting case - Prepare Safety...

**Mô tả công việc**: (Mức lương: 4 - 9 triệu VNĐ) **Introduction** Qualtech is an Asia Medical Device Consulting and Clinical Trial (CRO) Company with branch offices in China, Hong Kong, Indonesia, Japan, Malaysia, Philippines, Singapore, Vietnam, Thailand, Korea, USA and Germany. We are looking for a Talented Regulatory Affairs Intern who is...

**Regulatory/Reporting Specialist** **_ HCMC_** **Why Confluence?** Over the past several years we have undergone a great deal of positive change and growth to become the company we are today. Our global footprint now spans multiple countries, giving our employees the opportunity to get exposure to other countries and cultures. And it stands to reason...

$2,000 - $3,000 - FMCG **RESPONSIBILITIES**: As the Corporate Affairs Manager, you will be responsible for developing and implementing advocacy strategies to enhance company reputation and promote its interests among our stakeholders, working closely with the Line Manager. You will engage with key external stakeholders, including government agencies,...

Attractive Salary - Premium Healthcare - International working environment **A. Responsibilities**: Manage new product introduction for general chemicals, biocides, cosmetics and veterinary health products and more: - Provide direction to Marketing, R&D, Supply chain Operations, and Sales to facilitate speed to market and to maintain compliance with...

The Sr. Regulatory Compliance Specialist is a key position in the Regulatory Compliance organization. This position supports import, export and licensing functions and drives the daily compliance activities required under the company's trade compliance policy. Export Functions: The Sr. Regulatory Compliance Specialist is responsible for resolving potential...

$1,500 - $2,000 - Services **KEY RESPONSIBILITIES** - Monitor regulatory affairs and consolidate regulatory database by nurturing relationship with key government, ministries, authorities, associations to de-prioritize or moderate business impacts (i.e tax increase, EHW, RRP, Supply chain) in coordination with regional/global/local CA&C direction - Develop...

Identify and assess existing non-compliance regulatory issues and report their implications to relevant personnel. - Develop action plans to rectify non-compliance matters, seeking opinions from relevant authorities and guiding entities through implementation. - Ensure compliance with lobbying disclosures and ethics rules. - Collaborate with business...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

Job Id: 8644- City: Hồ Chí Minh City, Viet Nam- Department: - Function: Regulatory Science & Government Affairs- Employee Type: Permanent Full Time- Seniority Level: ExecutiveDescription: **Job Title**:Country Regulatory Lead **Reports To**: Regional Regulatory Lead, APAC **about upl**: - UPL is focused on emerging as a premier global provider of total...

This position is responsible for providing strategies for medical affairs within the assigned Therapeutic Areas (HIO- Hematology, Immunology, Oncology) and new launching products. He/she will contribute to the achievement of business success by putting the patient’s needs, diagnosis, access to our medicines, and safety into primary focus by leveraging the...

**JOB PURPOSE** - This position is responsible for providing strategies for medical affairs within the Therapeutic Area of Vaccines and new launching products. He/she will contribute to the achievement of business success by putting the patient’s needs, diagnosis, access to our medicines, and safety into primary focus by leveraging the understanding of...

**Mô tả công việc**: (Mức lương: Thỏa thuận) He/she will work in a fast-paced team environment and have opportunity to gain broad experience in various aspects of medical marketing job. The Medical Marketing Specialist plays a critical role in creating accurate, engaging, and informative content related to healthcare, medicine, and related...

Proclinical are recruiting for a Vietnam Regulatory Manager to join a pharmaceutical organisation. This role is on a permanent basis and is located in Ho Chi Minh City. *** **Responsibilities**: - Guide DAV engagement and meetings with DAV for the allocated projects when needed. - Guarantee that both electronic and paper regulatory reports archives are...

MAIN PURPOSE OF ROLE_ Knowledge base acquired from several years of experience in the area of Regulatory Affairs. Works independently. May instruct or coach other para-professionals. - MAIN RESPONSIBILITIES_ - As the Senior para-professional in the Regulatory Affairs Sub-Function, possesses advanced knowledge in directing development of product...

Clinical, Medical, Regulatory (CMR) Director **Category**:Clinical Development**Location**:Ho Chi Minh City, Vietnam, VN**About the Department*** - The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and...

Prudential's purpose is to help people get the most out of life. We will deliver our purpose by creating a culture in which diversity is celebrated and inclusion assured, for our colleagues, customers, and partners. We provide a platform for our people to do their best work and make an impact to the business, and in exchange, we support our people's career...