Sea Ra Manager

**Job Description Summary**:
**Key Responsibilities**:

- Manage execution of SEA ANZ Regulatory Affairs inclusive of processes, procedures, operational standards and systemically driven controls that ensure regulatory compliance and deliver market access for SEA ANZ.
- Provide guidance to regulatory personnel, project teams and other cross functional partners for tactical project execution, issue identification/mitigation, and assistance on various related topics (e.g. clinical trials, standards, advertising, testing requirements, product launch, etc.) in SEA ANZ countries with a regulatory framework.
- Ensure review and approval of promotional materials to comply with local regulatory requirements; manage local clinical trial submissions and SAE reporting (adverse events); analyze information on product recalls from field corrective action team and provide reports to local governments.
- Analyze local regulatory trends and market intelligence information; advise and make recommendations to leadership on potential high impact risks and change implementation; manage creation of local regulatory affairs strategy.
- Build and maintain relationships with internal regulatory affairs and cross-functional partners, local regulatory authorities and national and regional trade associations as requested; may act as a point of contact for regulatory authorities.
- Identify and evaluate registration, labeling and build process improvements and course alignment/correction opportunities.
- Ensure proactive maintenance and compliant entry of local submissions, approvals, and license expiries in the established regulatory database system.

**Required Education and Experience**:
Bachelor's Degree plus 8 years of experience in Regulatory Affairs or related field OR
Master's Degree plus 6 years of experience in Regulatory Affairs or related field
Other: Experience working in a healthcare company, regulatory affairs and medical device
Ability to fluently read, write and speak English

**Additional Skills**:

- Proven successful project management skills
- Proven expertise in both Microsoft Office Suite, including advanced Word, Excel and government regulatory systems
- Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
- Fluent in reading, writing and speaking English
- Extensive knowledge of regulatory affairs within the organization while contributing to the development of new concepts, techniques, and standards
- Extensive understanding of related aspects of product lifecycle processes and Critical Care Ignite system and government regulatory systems
- Extensive knowledge of Critical Care products
- Knowledge of healthcare industry
- Strict attention to detail
- Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization
- Ability to manage competing priorities in a fast paced environment
- Represents leadership on sections of projects within a specific area interfacing with country management teams (e.g. Business Unit head, Quality head, Ops head, Finance head)
- Consult in project setting within specific sections of regulatory affairs area
- Provides leadership to outsourcing partners of regulatory affairs consulting companies (e.g. on registration, labeling) on special projects
- Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

**Required Skills**:
Optional Skills


**Primary Work Location**: SGP The Strategy

**Additional Locations**:
**Work Shift**: