Regulatory Associate

Company: Unilever Thailand Holdings Business Function: Research & Development Job Title: Regulatory Affairs Assistant Manager, Thailand - Home Care Scope: Local Work Location: Unilever House Employment Type: Full Time The Purpose of Role: Regulatory Affairs (RA) role in Thailand is responsible for ensuring regulatory compliance of innovation projects...

Overview: Arxada is a pioneering leader with a powerful legacy: Over 120 years of creating specialty chemicals and solutions that potentiate the performance of our customers and their products. Our solutions, our expertise and our support help them to perform better - to be more efficient, more effective and more sustainable. We are passionate about...

**Regulatory Affairs - Supplements**: Bangkok Full Time and Permanent Nutrition 120,000 - 160,000 02 634 8884 **Regulatory Affairs - Supplements** - Being responsible for the registration of supplement products with the Thai FDA and other government agencies (including regulations of product registration, product classification, packaging and product...

**About us** **Since 1992, Device Technologies has been dedicated to improving patients’ lives through leading edge technology and services, **supplying hospitals and healthcare professionals with high-calibre medical solutions from around the world. Over 30 years, Device Technologies has developed a reputation for the quality, dedicated service and...

Job Title**:Regulatory Affairs - Ice Cream Thailand** Location**:Thailand** **Overview** We are committed to ensure that our products are compliant with legislation and that clear information is provided on their use and any risks that are associated with their use. To translate this mission efficiently into action, and to ensure that we comply with its...

C.U.N.T (TS) Representative in Association (ตัวแทนในสมาคม ผู้ประกอบธุรกิจกัญชา) **จังหวัด** กรุงเทพมหานคร (เขตบางรัก) **อัตราค่าจ้าง** 80k **รูปแบบงาน** งานประจำ (Full...

Minimum Qualifications & Experience: - Graduate in a clinical, pharmacy or life sciences related field. - At least 5 years' experience from a CRO or the pharmaceutical industry in activities related to trial start-up and/or regulatory operations - Through knowledge of applicable regulations - Able to manage in a matrix environment - Confident...

Regulatory Affairs Associate Manager - Position Title: Regulatory Affairs Assistant Manager - APAC - Work area: APAC - Regulatory Affairs - Reports To: Head, APAC - Global Regulatory Affairs - Location: Singapore/Thailand/Taiwan/Hong Kong - Job Responsibilities: - Support the regulatory management of Unilever H&W Vitamin, Mineral & Supplement (VMS) products...

**Minimum Qualifications & Experience**: Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. Preferably experience of working in the research, pharmaceutical...

**Minimum Qualifications & Experience**: - Graduate in a clinical, pharmacy or life sciences related field. - At least 1-2 years of related experience in either a CRO, pharmaceutical or clinical/hospital environment. **Responsibilities**: - Serve as the primary point of contact for the Regulatory Start Up Manager (RSM) and/or Project Manager (PM) during...

Blackmores Group is an Australian publicly-listed company, with an extensive presence across Asia Pacific. Our vision is to connect every person on earth to the healing power of nature by combining our knowledge of nature and science to deliver quality health solutions to people and their pets everywhere, every day. Recognising that you can’t have healthy...

**Job Description Summary**: To ensure all registration submissions in Thailand according to Curie project are completed and met timeline as planned. **Who We Are** **Main Responsibilities**: Responsible for all activities associated with regulatory clearance for all products in the country which includes: - Work closely with the Business Leads from the...

Job Description Summary To ensure all registration submissions in Thailand according to Curie project are completed and met timeline as planned. **Job Description**: Who We Are Main Responsibilities: Responsible for all activities associated with regulatory clearance for all products in the country which includes: - Work closely with the Business Leads...

Today, Lonza is one of the world’s largest healthcare manufacturing organizations operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers....

Experience in the company or corporate secretary. Strong knowledge of SEC/ SET rules, regulations. Fluent in English both written and verbal. **Responsibilities**: Serving as a news and information center for the directors, executives, and shareholders. Providing recommendations to the board on company businesses, as well as company regulations, articles of...

**Job Description Summary**: Provides regulatory strategy and direction to the Thailand business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance, working closely with healthcare regulatory bodies globally. In-depth understanding of key business drivers; uses this...

Overview: **We Are Kemin** We are visionaries who see things differently and are inspired by the world around us. We have been dedicated to using applied science to improve the quality of life for over half a century. Committed to feed and food safety, Kemin maintains top-of-the-line manufacturing facilities where over 500 specialty ingredients are made for...

**Key Responsibilities**: - Prepare and review product registration tasks covering the new product registration, progress reports, supplements, amendment, periodic reports and the renewal registration. - Maintain good relationship with government authorities to keep up to date on regulations changes and trends; seek advice on interpretation of government...

Core Responsibilities: - Serve as the primary point of contact for the Regulatory Start-Up Manager (RSM) and/or Project Manager (PM) during start-up on allocated projects. - Provide expertise and guidance to RSM and/or PM on country and local regulations and practices, keeping abreast of developments and changes in regulations, guidelines and practices...

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the study protocol and...