Regulatory Affairs Manager, Asia

**The Role**: **Where you fit in** Shell Energy Ambitions envisage trading a full range of gas/LNG and clean power products in new countries and being a leader in the provision of cleaner energy. Understanding the complex regulatory environment for gas and gas decarbonization, translating regulations into winning and defensive commercial structures,...

**About APACMed** Founded in 2014, the Asia Pacific Medical Technology Association (APACMed) is the first and only regional MedTech association in APAC, representing medical technology manufacturers (multinational corporations as well as small and medium enterprises), and local industry associations across the region. We are fully committed to facilitating...

Roles & ResponsibilitiesThis position will be responsible for the management of product registrations, product compliance or product safety and risk assessment for Animal Nutrition & Health. IFF applies expert science to advance market-driven, healthy, and sustainable solutions for the food/feed, beverage, dietary supplements, and many other industries. The...

**Responsibilities**: - Lead and supervise the SG Regulatory Affairs (RA) - Accountable for all Products Registration, renewals, and amendments - Communicate with regulatory authorities as well as regional RA team regarding regulatory affairs matters such as product registrations, changes in existing products and renewals. - Advise internal stakeholders on...

COMPANY DESCRIPTION As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the world’s growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create...

This is a full-time hybrid role as a Regulatory Affairs Manager at Artixio. The Regulatory Affairs Manager will be responsible for ensuring regulatory compliance, managing regulatory requirements, overseeing regulatory submissions, and maintaining quality systems. The role is based in Singapore but allows for some remote work. **Qualifications** - Minimum...

** Join the premier biopharmaceutical company** that has been in Asia Pacific for over 60 years. - Bring your **entrepreneurial** **curiosity** and **learning spirit **into a career of **purpose**, **personal growth**, and **leadership.** - Your chance to be in a regional leadership role and at the centre of strategic excellence. Our Regulatory Affairs team...

Roles & ResponsibilitiesRoles & ResponsibilitiesThe RAQA Manager is responsible for overseeing regulatory compliance and quality affair functions within the organization. The RAQA Manager will work closely with the Head of RAQA and cross- functionally with teams including R&D, Product Development and Operations teams to ensure regulatory requirements and...

Full awareness of local Health Products and Medical Device Act and their regulations relevant to the business through regularly checking HSA websites and attending HSA briefings; - Communicate changes and new requirements to management; - Meet, discuss and negotiate with HSA regulators on matters pertaining to product registrations; - Have working knowledge...

Roles & ResponsibilitiesYour new company Our client is a fast growing food and beverages company, with a strong presence across Asia. They are looking for an experienced Regulatory Affairs Lead to help them grow their regulatory team here in Singapore.Your new roleBelow are some of the key responsibilities for the role;· Develop and implement regulatory...

APAC regulatory affairs - Pharmaceutical industry - Singapore registered pharmacist Reporting to the Head of Regulatory Affairs, you will be responsible for assimilating knowledge of scientific, regulatory, and business issues to enable products that are developed, manufactured or distributed to meet required legislation. You will provide strategic...

**Job Details**: **Location** Singapore **Salary** Competitive Salary **Job Type** Permanent **Ref** BH-178593 **Contact** Piers Atkinson- **Posted** about 1 hour ago - A new entrant to Asia, this Biopharma is looking for a Regulatory Affairs Associate Director. - You will be in charge of all things regulatory in APAC where currently they don’t...

The Regulatory Affairs (RA) CMC Manager for APAC independently manages all regulatory CMC aspects of assigned Kyowa Kirin projects / products. This includes Biologics, Small Molecules, and Drug/Device combinations. Has sound understanding and experience in navigating Asia Pacific (APAC) regulatory environment as well as managing interactions with APAC...

6 Months Contract **Responsibilities**: - Responsible for regulatory activities and quality assurance in SE Asia - Timely coordination and submission of product registration and follow up request i.e. new products, license renewals and product amendments. This would include product grouping and risk classification, and regular update of the database - Post...

Develop and implement regulatory strategies to secure product approvals more quickly than competitors. - Lead complex decision-making processes among stakeholders and senior leadership in a dynamic regulatory environment. - Provide expert advice on regulatory strategy, Health Authority engagement, and submission activities for the IVD product lines. -...

**Job Details**: **Location** Singapore **Salary** Competitive Salary **Job Type** Permanent **Ref** BH-179384 **Contact** Roselle Cuntapay **Posted** about 3 hours ago - Currently recruiting for a Regulatory Affairs Specialist for a small Medical Device business. Their product is currently in a couple of markets (and doing well) but they are...

**Duties**: - Manage renewal processes of medical device for maintaining regulatory compliance - Facilitate the dissemination of documentation (eg. Letter of Authorization, Free Sales Certificates, Certificates of Origin, etc) to both internal and external parties - Serve as internal consultant for basic regulatory affairs support involving issues such as...

**PURPOSE OF JOB** Subject matter expert in determining the current regulatory requirements and strategies for Merit Medical Singapore design control projects. Prepare documents and /or submission required to obtain clearance or approval from government agencies for commercial distribution of Merit’s Medical Devices. Key government agencies with direct...

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of...

**Your Job**: The Director, Regulatory Affairs - APAC K-C Professional (KCP) & Consumer leads the regional regulatory affairs team for APAC (Asia-Pacific, Australia & China), and is responsible for establishing, implementing and maintaining required regulatory compliance for the business. The APAC Regulatory Affairs team provides strategic regulatory...