410 Corporate Governance jobs in Vietnam

Our client is seeking a meticulous and knowledgeable Pharmaceutical Regulatory Affairs Specialist to ensure compliance with all relevant pharmaceutical regulations and guidelines. This hybrid role offers a balance of remote work and in-office collaboration in Haiphong, Hai Phong, VN . You will be responsible for preparing, reviewing, and submitting regulatory documentation for drug applications, amendments, and renewals to health authorities. Key duties include staying abreast of evolving regulatory requirements, assessing the impact of changes on existing products, and providing regulatory guidance to internal teams, including R&D, manufacturing, and quality assurance. You will also manage post-market surveillance activities and ensure ongoing compliance. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field, coupled with significant experience in pharmaceutical regulatory affairs. A thorough understanding of regulatory submission processes, guidelines (e.g., ICH, FDA, EMA), and drug development lifecycle is crucial. Excellent written and verbal communication skills are essential for preparing clear and concise regulatory documents and communicating effectively with regulatory agencies and internal stakeholders. Strong analytical and problem-solving skills are required to navigate complex regulatory challenges. This position demands a high level of accuracy, attention to detail, and the ability to manage multiple projects with strict deadlines. You will be a key contributor to ensuring the timely approval and continued market access of our client's pharmaceutical products. Join a team dedicated to advancing healthcare through rigorous adherence to regulatory standards.

**Requistion ID** : 80589
Dentsply Sirona is the world's largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona's products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona's global headquarters is located in Charlotte, North Carolina, USA. The company's shares are listed in the United States on NASDAQ under the symbol XRAY.
**Bringing out the best in people**
As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we're looking for the best to join us.
Working at Dentsply Sirona you are able to:
**Develop faster** - with our commitment to the best professional development.
**Perform better** - as part of a high-performance, empowering culture.
**Shape an industry** - with a market leader that continues to drive innovation.
**Make a difference** -by helping improve oral health worldwide.
**Position Summary:**
Supports regulatory affairs activities for medical device licenses in Vietnam.Manages requests for and strategically plan work related to registration activities in Vietnam. Manages projects and/or regulatory affairs for the assigned Location(s)/Region(s).
**Key Responsibilities**
+ Develops and implements regulatory strategies to obtain and maintain regulatory approvals for medical devices
+ Leads and manages regulatory submissions
+ Manage communications with authorities on behalf of the company for market access related submissions
+ Reviews and interprets regulatory requirements and guidance documents to ensure compliance
+ Coordinates regulatory activities with internal teams and external regulatory agencies
+ Review and approve product labelling
+ Stays current with regulatory requirements and updates affecting medical devices
+ Fosters professional interactions with internal and external stakeholders through various communication channels, enhancing business relationships
+ Complies with company and departmental policies and administrative requirements
+ Performs other duties as assigned or as needed
**Typical Background**
**Education:**
+ Bachelor's degree in a relevant field, such as life sciences, regulatory affairs, or a related discipline.
**Language:**
+ Fluent in written, reading, spoken and listening English.
+ Fluent in written, reading and spoken Vietnamese
**Years and Type of Experience:**
+ 5(+) years of experience in Vietnam regulatory affairs, preferably in the medical device industry
+ Knowledge of Vietnamese Regulations and classifications
+ Knowledge of FDA regulations and international standards (e.g., ISO 13485, MDSAP, EU MDR)
+ Experience with software as a medical device, AI and/or medical devices containing software is a plus
**Required Computer / Software Skills:**
+ Proficiency with Microsoft Office Suite
**Key Required Skills, Knowledge, and Capabilities:**
+ Strong leadership, project management, and organizational skills, including attention to detail
+ Excellent communication (both written and verbal) and interpersonal skills
+ Ability to work effectively in a team environment, as well as independently
+ Willingness to learn and adapt to new processes and technologies
**Key Leadership Behaviors**
+ Actively articulates and promotes Dentsply Sirona's vision and direction
+ Advocates on behalf of the customer
+ Values driven with an insistence on excellence
+ Promotes high performance, innovation, and continual improvement
+ Consistently meets Company standards, ethics, and compliance requirements
+ Strong results orientation and analytical skills
+ Clear and effective communication with key stakeholders, which span across multiple levels, socio-geographic areas, and functional expertise
+ Resolves conflicts and fosters a positive working environment
+ Be a change leader
Dentsply Sirona is an Equal Opportunity/ Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, disability, or protected Veteran status. We appreciate your interest in Dentsply Sirona.
If you need assistance with completing the online application due to a disability, please send an accommodation request to ( ) . Please be sure to include "Accommodation Request" in the subject.

-Job Advert Details

**Some careers have more impact than others.**
- If you’re looking for a career where you can make a real impression, join HSBC and discover how valued you’ll be. Whether you want a career that could take you to the top, or simply take you in an exciting new direction, HSBC offers opportunities, support and rewards that will take you further.

**Global Functions (GFs) **play a vital role in supporting the bank’s Global Businesses and offer a broad range of career opportunities in areas from legal, risk and finance to human resources, sustainability, marketing and communications. Their operational and functional teams around the world help HSBC’s Global Businesses to operate efficiently and effectively on a day-to-day basis. They also focus on controls and governance to reduce risk and protect the Group’s reputation
**.**

We are currently seeking a high caliber professional to join our team as an **Manager, Corporate Governance and Company Secretary.**

**Principal Accountabilities**

Impact on the Business
- Develop and maintain information flows to and within the Members’ Council and the Board of Supervision or other country-level management committees if so required and between senior management and members. Prepare and present papers and memoranda to and communicate appropriate recommendations for action. Timely preparation of Minutes of governance meetings at which he/she acts as the secretary
- Prepare and submit documents to government regarding the corporate registration/filing and appointments of Council members, Board of Supervision members and the CEO.
- Provide timely and reliable advice to Council members, Board of Supervision members or other management committees on their collective and individual responsibilities and assistance with the discharge of their statutory and regulatory obligations. Introduce tailored induction programmes for new Council Members and Board of Supervision members, and arrange development activities as appropriate.

**Customers / Stakeholders**
- Navigate between senior stakeholders in HBVN on all board/committee governance matters.
- Provide direct support and advices to the Members’ Council and the Board of Supervision or other country-level management.
- Maintain and develop positive relationships with Group and regional stakeholders within the CG&S function and advise on corporate governance matters in Vietnam.

**Leadership & Teamwork**
- The role holder is largely an individual contributor but need to maintain and develop positive and professional working relationships with senior stakeholder at Group, regional and country level.
- Contribute to the strategy for the coordination and promotion of initiatives that result in the sharing of company secretarial/ governance knowledge and best practice.

**Operational Effectiveness & Control**
- Regularly assess the operational and cost efficiency within areas of business.
- Re-engineer existing processes to deliver efficiencies within the Department.
- Responsible for the development and implementation of policy and procedures in adherence to Group policies and management of operational risk.
- Oversee all regulatory and compliance matters and the management of operational risk
Qualifications
- A minimum of 5 years relevant working experiences focusing on general corporate matters;
- Knowledge and insights on Company Law of Vietnam and corporate registration practice;
- Knowledge of legal framework of Vietnam is desirable
- Proficiency in English;
- Detailed knowledge of the HSBC Group and a clear understanding of its corporate culture is desirable.
- Leadership, management and communication skills.
- Lateral thinking/problem solving/creativity.

You’ll achieve more when you join HSBC.

Issued by The Hongkong and Shanghai Banking Corporation Limited

Our client, a renowned pharmaceutical company, is seeking an experienced Senior Pharmaceutical Regulatory Affairs Specialist to join their team based in Phan Thiet, Binh Thuan, VN . This role is critical for ensuring compliance with all national and international pharmaceutical regulations, facilitating the smooth approval and lifecycle management of medicinal products. You will play a key role in preparing and submitting regulatory dossiers, interacting with health authorities, and providing expert regulatory guidance throughout the product development process.

Key Responsibilities:

• Prepare, review, and submit regulatory documentation for drug product registrations, variations, and renewals to health authorities.
• Ensure all regulatory submissions are accurate, complete, and adhere to current guidelines and standards.
• Develop and implement regulatory strategies for new product development and lifecycle management.
• Liaise with national and international regulatory agencies, responding to queries and facilitating communication.
• Monitor changes in the regulatory landscape and assess their impact on the company's products and operations.
• Provide regulatory guidance and support to internal teams, including R&D, manufacturing, quality assurance, and marketing.
• Review promotional materials and product labeling for regulatory compliance.
• Manage post-approval regulatory activities, such as annual reports and safety updates.
• Conduct regulatory due diligence for potential business development opportunities and partnerships.
• Maintain up-to-date knowledge of pharmaceutical regulations, guidelines, and best practices.

Qualifications:

• Bachelor's or Master's degree in Pharmacy, Chemistry, Life Sciences, or a related field.
• Minimum of 6 years of experience in pharmaceutical regulatory affairs.
• In-depth knowledge of drug development processes and regulatory submission requirements in key markets.
• Proven experience in preparing and submitting CTD (Common Technical Document) or equivalent dossiers.
• Familiarity with relevant regulatory guidelines (e.g., ICH, FDA, EMA, local regulatory authority guidelines).
• Strong analytical, problem-solving, and project management skills.
• Excellent written and verbal communication skills, with meticulous attention to detail.
• Ability to work effectively both independently and as part of a collaborative team.
• Proficiency in regulatory information management systems and databases.
• Experience in specific therapeutic areas is a plus.

This position requires your presence at our office in Phan Thiet, Binh Thuan, Vietnam. We offer a competitive compensation package and the opportunity to grow within a dynamic pharmaceutical environment.

Our client, a globally recognized pharmaceutical company dedicated to advancing healthcare solutions, is actively seeking a meticulous and experienced Remote Pharmaceutical Regulatory Affairs Specialist. This position is vital for ensuring compliance with global regulatory requirements for drug development and market authorization. As a remote employee, you will play a key role in preparing and submitting regulatory dossiers, liaising with health authorities, and providing strategic regulatory guidance throughout the product lifecycle. Your responsibilities will include developing regulatory strategies for new drug applications (NDAs), managing post-approval changes, and monitoring evolving regulatory landscapes in key markets. You will also be responsible for ensuring that all company activities related to pharmaceutical product registration and maintenance meet the highest standards of compliance. Collaboration with cross-functional teams, including R&D, clinical operations, and quality assurance, is paramount. This fully remote role requires a Bachelor's or Master's degree in Pharmacy, Chemistry, Life Sciences, or a related discipline, complemented by a minimum of 4 years of direct experience in pharmaceutical regulatory affairs. A deep understanding of ICH guidelines, FDA, EMA, and other major regulatory agency requirements is essential. Excellent written and verbal communication skills, meticulous attention to detail, and strong project management capabilities are required. Experience with regulatory information management systems is a plus. If you are a dedicated regulatory professional passionate about bringing life-saving medicines to patients worldwide, this remote opportunity offers a platform to make a significant impact.

Our client is seeking an experienced Remote Pharmaceutical Regulatory Affairs Specialist to join their international team. This is a fully remote position, ideal for professionals who thrive in a flexible work environment and possess a strong command of global pharmaceutical regulations. You will be responsible for preparing, submitting, and managing regulatory filings for new drug applications (NDAs), variations, and annual reports in various international markets. Your role will involve interpreting and applying regulatory guidelines from agencies such as the FDA, EMA, and other health authorities to ensure compliance throughout the product lifecycle. You will liaise with regulatory agencies, respond to queries, and support regulatory inspections. Key responsibilities include developing regulatory strategies, assessing the regulatory impact of changes, and ensuring that all promotional materials and labeling comply with regulations. The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Life Sciences, Chemistry, or a related field, with at least 5 years of direct experience in pharmaceutical regulatory affairs. A thorough understanding of drug development processes and regulatory submission requirements is essential. Strong written and verbal communication skills, meticulous attention to detail, and the ability to manage multiple projects simultaneously are crucial. Experience with regulatory information management (RIM) systems is highly preferred. This role demands an organized, proactive, and detail-oriented individual capable of navigating complex regulatory landscapes from a remote setting. This is an outstanding opportunity to contribute to bringing life-saving medicines to patients worldwide.

Our client , a leading pharmaceutical company, is seeking a highly experienced Senior Pharmaceutical Regulatory Affairs Specialist. This role is crucial for ensuring compliance with all relevant health authority regulations during drug development and lifecycle management. You will be responsible for preparing and submitting regulatory dossiers, responding to health authority queries, and staying abreast of evolving regulatory landscapes.

Key responsibilities include developing regulatory strategies for new product submissions, managing post-approval changes, and ensuring compliance with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and Good Pharmacovigilance Practices (GVP). You will liaise with internal departments, external partners, and regulatory agencies worldwide. The ideal candidate will possess a strong understanding of drug development processes, regulatory submission requirements in key markets, and have excellent scientific, written, and verbal communication skills.

We are looking for a detail-oriented individual with strong analytical and problem-solving abilities. Experience with electronic submission formats and regulatory databases is expected. This position offers a hybrid work arrangement, requiring occasional attendance at our facility in Thanh Hoa, Thanh Hoa, VN . Your expertise will be vital in accelerating the approval process for new and existing pharmaceutical products, contributing to patient access to innovative treatments. Join a dedicated team focused on advancing healthcare through rigorous regulatory compliance.

**ABOUT ABBOTT**
Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, anticipating changes in medical science and technology.
**WORKING AT ABBOTT**
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
+ Career development with an international company where you can grow the career you dream of.
+ A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
**MAIN PURPOSE OF ROLE**
+ Product registration including new, renewal, variations, special import license, promotional materials.
+ Do regulatory activities to support product circulation in the market i.e. tender support, GMP listing, stock management.
+ Other tasks assigned by the line manager.
**MAIN RESPONSIBILITIES**
+ Contact with DAV, MOH and relevant Authorities:Liaise with government to ensure regulatory compliances.Establish and maintain positive relationship with government agencies and other regulatory authorities.
+ Coordinate with manufacture, region and prepare dossier for product registration (drug, health supplement.) following the regulation. Supervise the registration of marketed product.
+ Liaison with various distributors/consultants/DAV (Drug Administration of Vietnam) to facilitate the smooth registration activity
+ Understand and share current updates in regulations/new guidelines/circulars published by DAV
+ Evaluate and review registration dossiers for administration
+ Keep track of registration status, submissions and registration timeline
+ Closely follow up the status of application from the time of submission until getting approval
+ Support Marketing team in applying advertisement licenses & detail aid material printing permits
+ Monitor and disseminate information on changes to regulations affecting registration, manufacture, distribution and sale of Abbott products.
**MINIMUM BACKGROUND/ EXPERIENCE REQUIRED**
**Work Experience:** >3 years experience in Regulatory, prefer pharmaceutical MNC
**CORE Skills Required:**
_Professional Skill_
+ Time management
+ Persuasiveness
+ Good in working arrangement, teamwork
+ Honest, careful, patient, highly responsible
_Behavioral / Leadership Skill:_ Apply Abbott Capabilities Framework
_Language Skill:_ Vietnamese/ Tiếng Việt & English/Tiếng Anh
_Computer Skill:_ MS office
**MINIMUM EDUCATION REQUIRED**
+ Bachelor's degree in Pharmacist or Medical Doctor
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

**Mô tả công việc**:
(Mức lương: Thỏa thuận)
- Conduct risk assessment of current product and service flows of Got It. Propose the solutions to prevent risks & build solutions to control risks.
- Be involved in upcoming projects, assess, analyze risks and suggest solutions to prevent and minimize them from the beginning.
- Analyze data & user behavior, identify & analyze unusual trends and propose plans to limit risks.
- Build, manage and continuously improve policies and regulations to limit fraud and risks in all company products and services.
- Be involved in building and monitoring of risk and fraud management tools of the system.
- Coordinate with other departments when there are incidents related to risks and frauds.
- Periodically review risk and fraud regulations to ensure that regulations are still valid and appropriate;
- Assist to evaluate, check and detect security errors in the system.
- Conduct the training of risk awareness and information security for employees.
- Perform tasks as assigned by Line Manager

**Chức vụ**: Trưởng Nhóm/Trưởng Phòng

**Hình thức làm việc**: Toàn thời gian

**Quyền lợi được hưởng**:

- Quality work environment, flexibility, being innovative and rewarded for efforts.
- Good chance to study and develop a career path stably.
- Statutory insurance on 100% gross salary as per law
- 100% gross salary during probation time
- Company trip, team building, internal activities, medical checkup
- Bao Viet Healthcare insurance.

**Yêu cầu bằng cấp (tối thiểu)**: Trung cấp - Nghề

**Yêu cầu công việc**:

- Bachelor degree in IT/Computer Science, or equivalent educational background
- At least 3 years of experience in risk management or relevant positions
- Knowledge of information system & new technologies
- Deep knowledge of information security & risk assessment
- Experience in pentest is a plus
- Having certificates of security or used to be work in risk management or information security procedures project (such as ISO) is a plus
- Ability to understand & analyze data
- Ability to manage project & timeline
- Good communication & problem solving skill
- Be integrity, careful, accurate
- Ability to work independently & teamwork while using discretion in decision making and sound judgment in problem solving.

**Yêu cầu giới tính**: Nam/Nữ

**Ngành nghề**: CNTT - Phần Mềm,Quản Trị Rủi Ro

Trung cấp - Nghề
Không yêu cầu