Regulatory Affairs Lead

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...

Job OverviewThis role is responsible for all domestic and regional regulatory affairs, including submissions to government agencies. Key Responsibilities: Preparation and documentation of regulatory submissions. Establishing pharmacovigilance for products. The ideal candidate will have a degree in any science-related field and 3 years of experience in...

Roles & ResponsibilitiesFormulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced Oversee documentation efforts to ensure compliance with local and international regulations and standards. Develop and maintain standard operating procedures. Develop regulatory strategies and...

Roles & ResponsibilitiesFormulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced Oversee documentation efforts to ensure compliance with local and international regulations and standards. Develop and maintain standard operating procedures. Develop regulatory strategies and...

Roles & ResponsibilitiesOverviewThe Project Manager, Regulatory Affairs, plays a pivotal role in driving APACMed's Regulatory Affairs (RA) agenda across the Asia-Pacific region. The position involves managing complex RA initiatives, fostering collaboration among stakeholders, and ensuring the successful delivery of high-impact projects aligned with the...

Roles & ResponsibilitiesPosition: REGULATORY AFFAIRS MANAGER (1 vacancy - immediate)Job Description (all processes will be taught in-house):· Co-ordination and online submission of various formatted documentation to the Health Sciences Authority (Ministry of Health)· Compiling of client's dossiers for medical devices and applications as per Ministry's...

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...

Roles & ResponsibilitiesOverviewThe Project Manager, Regulatory Affairs, plays a pivotal role in driving APACMed's Regulatory Affairs (RA) agenda across the Asia-Pacific region. The position involves managing complex RA initiatives, fostering collaboration among stakeholders, and ensuring the successful delivery of high-impact projects aligned with the...

Roles & ResponsibilitiesPosition: REGULATORY AFFAIRS MANAGER (1 vacancy - immediate)Job Description (all processes will be taught in-house):· Co-ordination and online submission of various formatted documentation to the Health Sciences Authority (Ministry of Health)· Compiling of client's dossiers for medical devices and applications as per Ministry's...

Role SummaryThe Regulatory Affairs Specialist will be responsible for all domestic and regional regulatory affairs, including but not limited to NDAs, variations, and registration renewals. Main Responsibilities: Preparation of regulatory submissions. Maintenance of tracking logs and supply of global registration requests. Monitoring FDA and other agency...

Job OverviewThe Private Advertiser seeks a highly skilled Regulatory Affairs Specialist to oversee the product registrations and regulatory pathways in Asia Pacific. This role requires strong expertise in ensuring compliance with Asia Pacific regulations, influencing key decision-making processes, and contributing to enterprise-wide impact.Main...

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear...

Roles & ResponsibilitiesJob title – Regulatory Affairs Manager, APAC Animal Nutrition & HealthLocation – SingaporeJob model – HybridTo provide support to Greater APAC Animal Nutrition and Health (ANH) Regulatory Affairs Team. To lead and manage Regulatory Affairs professionals. Responsible for product registration activities, maintenance of regulatory...

We are seeking an experienced Regulatory Affairs Manager to join our team at Cambridge Advisers PTE. LTD.About the Role:The successful candidate will be responsible for managing corporate bank accounts, conducting KYC/CDD checks, and ensuring compliance with AML regulations. They will also advise clients on market entry strategies and compliance...

Roles & ResponsibilitiesResponsibilitiesQuality Assurance:Overall implementation and maintenance of the Quality Management System (QMS) in compliance with ISO 13485 and 21 CFR 820 standards. Ensure all departments carry out due processes and documentation required to ensure conformance to the QMS, including design & development, production and software. ...

Roles & ResponsibilitiesSummaryWe are seeking a highly motivated and detail-oriented Senior Regulatory Affairs Executive to join our team. In this role, you will be responsible for managing the drug registration process for our innovative pharmaceuticals across Southeast Asia. You will work closely with regulatory agencies, internal stakeholders, and...

Roles & ResponsibilitiesOur client is a global pharmaceutical company with a wide product portfolioDevelop and implement regulatory strategies for new and existing products in the assigned regions. Provide guidance to the company regarding regulatory requirements and ensure compliance with all relevant regulations. Submission and coordination with H.S.A....

Roles & ResponsibilitiesJob Description:Manage document control process for Quality Management Systems in compliance with ISO13485, GDPMDS and any other standards as appropriate Assists in meeting the company's objectives and sales goals by your effort in implementing smooth workflows and processes to have a highly efficient and functional sales support...

At Givaudan, you will contribute to creating delightful taste and scent experiences that touch people's lives.You will work within an inspiring teamwork culture where you can thrive, collaborate, and learn from other talented and passionate people across disciplines, regions, and divisions.Givaudan embraces diversity and is committed to building an inclusive...

Key ResponsibilitiesAs a Regulatory Affairs E-Doc Assistant, your key responsibilities will include:Preparing and delivering product information and technical documentation in a timely manner, according to customers' needs and regulatory requirements.Using Givaudan systems to complete tasks and manage data.Consulting with senior Regulatory team members for...