201 Quality Assurance Analyst jobs in Vietnam
Senior Pharmaceutical Quality Assurance Analyst
650000 Nha Trang, Khanh Hoa
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Job Description
Our client, a leading pharmaceutical company dedicated to developing life-changing medicines, is seeking a highly experienced Senior Pharmaceutical Quality Assurance Analyst to join their esteemed team in **Nha Trang, Khanh Hoa, VN**. This hybrid role involves ensuring the highest standards of quality and compliance throughout the drug development lifecycle. The ideal candidate possesses a meticulous attention to detail and a deep understanding of regulatory requirements.
Key Responsibilities:
Key Responsibilities:
- Develop, implement, and maintain quality assurance systems and procedures in accordance with cGMP and other relevant regulatory guidelines.
- Conduct internal audits and inspections of manufacturing processes, facilities, and documentation.
- Review and approve batch records, validation protocols, and reports.
- Investigate deviations, out-of-specifications (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
- Participate in regulatory agency inspections and prepare responses.
- Develop and deliver quality training programs for personnel.
- Monitor and analyze quality metrics to identify trends and areas for improvement.
- Ensure compliance with all applicable regulatory requirements, including FDA, EMA, and local regulations.
- Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs.
- Stay current with evolving regulatory landscapes and industry best practices.
- Lead or participate in supplier qualification and audits.
- Manage change control processes effectively.
- Contribute to the continuous improvement of the Quality Management System (QMS).
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 6 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- In-depth knowledge of Good Manufacturing Practices (GMP), ICH guidelines, and regulatory affairs.
- Experience with electronic Quality Management Systems (eQMS).
- Strong understanding of validation principles for processes, equipment, and analytical methods.
- Excellent analytical, problem-solving, and critical thinking skills.
- Meticulous attention to detail and commitment to quality.
- Strong written and verbal communication skills, with the ability to clearly document findings and recommendations.
- Proficiency in Microsoft Office Suite.
- Ability to work effectively both independently and as part of a collaborative team.
- Experience with data analysis and statistical tools is desirable.
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0
Remote Senior Quality Assurance Analyst
10000 An Cu, An Giang
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Our client is seeking a highly skilled and meticulous Remote Senior Quality Assurance Analyst to join their innovative software development team. This fully remote position is crucial for ensuring the delivery of high-quality, bug-free software products. You will be responsible for designing, developing, and executing comprehensive test plans and test cases, identifying, documenting, and tracking defects, and collaborating closely with developers and product managers to resolve issues. The ideal candidate possesses a deep understanding of QA methodologies, automation tools, and a passion for delivering excellent user experiences.
Responsibilities:
Qualifications:
If you are passionate about software quality and thrive in a remote work environment, we invite you to apply.
Responsibilities:
- Design, develop, and execute detailed test plans, test cases, and test scripts for web and mobile applications.
- Perform various types of testing, including functional, regression, integration, performance, and user acceptance testing (UAT).
- Identify, document, and track software defects using bug tracking systems (e.g., Jira, Bugzilla), providing clear and concise reproduction steps.
- Collaborate closely with software developers and product managers to understand requirements and ensure test coverage meets project goals.
- Develop and maintain automated test scripts using relevant testing frameworks and tools.
- Analyze test results, generate test reports, and provide feedback on product quality to stakeholders.
- Participate in agile development processes, including sprint planning, daily stand-ups, and retrospectives.
- Advocate for quality throughout the development lifecycle and contribute to the continuous improvement of QA processes and methodologies.
- Mentor junior QA analysts and share best practices.
- Stay up-to-date with the latest QA tools, technologies, and industry trends.
- Ensure all testing is conducted in accordance with project requirements and quality standards.
- Provide insights into product usability and user experience from a QA perspective.
Qualifications:
- Bachelor's degree in Computer Science, Engineering, or a related technical field, or equivalent practical experience.
- Minimum of 5 years of experience in software quality assurance, with at least 2 years in a Senior QA role.
- Strong understanding of SDLC, Agile methodologies, and QA best practices.
- Proficiency in manual and automated testing tools (e.g., Selenium, Appium, Postman).
- Experience with bug tracking and test management tools (e.g., Jira, TestRail).
- Knowledge of programming or scripting languages (e.g., Java, Python, JavaScript) for test automation.
- Excellent analytical, problem-solving, and debugging skills.
- Strong communication and collaboration skills, with the ability to work effectively in a remote team environment.
- Detail-oriented with a commitment to accuracy and thoroughness.
- Experience with API testing and performance testing is a plus.
- Relevant certifications (e.g., ISTQB) are advantageous.
If you are passionate about software quality and thrive in a remote work environment, we invite you to apply.
This advertiser has chosen not to accept applicants from your region.
1
Remote Pharmaceutical Quality Assurance Analyst
500000 An Thanh
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Job Description
Our client is seeking a highly diligent and meticulous Pharmaceutical Quality Assurance Analyst to join their esteemed team in a fully remote capacity. This role is crucial for upholding the highest standards of quality and compliance within our pharmaceutical operations. The ideal candidate will possess a strong understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory requirements specific to the pharmaceutical industry. You will be responsible for reviewing and approving batch records, conducting internal audits, investigating deviations and out-of-specification (OOS) results, and ensuring all quality control procedures are followed meticulously. As a remote team member, you will collaborate closely with manufacturing, quality control, and regulatory affairs departments, utilizing digital platforms for data sharing, analysis, and communication. This position requires exceptional analytical skills, a keen eye for detail, and the ability to interpret complex scientific data. We are looking for a proactive individual who can identify potential quality issues, implement corrective and preventive actions (CAPAs), and contribute to the continuous improvement of quality systems. Experience with quality management software (QMS) and a thorough knowledge of pharmaceutical development and manufacturing processes are essential. If you are a dedicated QA professional passionate about ensuring product safety and efficacy and seeking a challenging remote role within the pharmaceutical sector, we encourage you to apply.
Responsibilities:
Responsibilities:
- Review and approve pharmaceutical batch records and documentation.
- Conduct internal audits and ensure compliance with GMP/GLP standards.
- Investigate deviations, OOS results, and customer complaints.
- Develop and implement corrective and preventive actions (CAPAs).
- Ensure all quality control procedures are accurately performed and documented.
- Collaborate with manufacturing and R&D teams on quality-related matters.
- Maintain and improve the company's Quality Management System (QMS).
- Stay updated on regulatory guidelines and industry best practices.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 4 years of experience in Pharmaceutical Quality Assurance or Quality Control.
- In-depth knowledge of GMP, GLP, and regulatory guidelines (e.g., FDA, EMA).
- Experience with quality management systems and deviation investigations.
- Strong analytical skills and attention to detail.
- Excellent written and verbal communication skills.
- Ability to work independently and effectively in a fully remote environment.
This advertiser has chosen not to accept applicants from your region.
2
Senior Pharmaceutical Quality Assurance Analyst
900000 Can Tho , Can Tho
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Posted today
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Job Description
Our client, a reputable pharmaceutical company, is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Assurance Analyst to join their operations in **Can Tho, Can Tho, VN**. This role is critical for ensuring that all pharmaceutical products meet the highest standards of quality and regulatory compliance. The ideal candidate will have a robust understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines. You will be responsible for developing, implementing, and maintaining quality assurance systems and procedures throughout the product lifecycle, from raw material testing to finished product release. This position requires a keen eye for detail, strong analytical skills, and the ability to work collaboratively with R&D, manufacturing, and regulatory affairs teams.
Key Responsibilities:
Qualifications:
This is an excellent opportunity for a seasoned QA professional to make a significant impact in a growing pharmaceutical company. Our client offers a competitive salary and benefits package, along with opportunities for professional development and career advancement.
Key Responsibilities:
- Develop, implement, and manage quality assurance programs and procedures.
- Conduct audits of manufacturing processes, documentation, and facilities to ensure compliance with GMP and regulatory standards.
- Review and approve batch records, validation protocols, and technical reports.
- Perform quality control testing on raw materials, in-process samples, and finished products.
- Investigate deviations, non-conformances, and customer complaints, and implement corrective and preventive actions (CAPA).
- Prepare and submit regulatory documentation to health authorities.
- Stay up-to-date with evolving regulatory requirements and industry best practices.
- Collaborate with cross-functional teams to ensure quality is integrated into all stages of product development and manufacturing.
- Train personnel on quality assurance procedures and GMP principles.
- Participate in regulatory inspections and client audits.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 7 years of experience in pharmaceutical quality assurance or quality control.
- In-depth knowledge of GMP, GLP, ICH guidelines, and FDA regulations.
- Experience with quality management systems (QMS) and document control.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills, with the ability to effectively document findings and recommendations.
- Proficiency in laboratory equipment and analytical techniques.
- Detail-oriented with a commitment to accuracy and compliance.
This is an excellent opportunity for a seasoned QA professional to make a significant impact in a growing pharmaceutical company. Our client offers a competitive salary and benefits package, along with opportunities for professional development and career advancement.
This advertiser has chosen not to accept applicants from your region.
3
Remote Pharmaceutical Quality Assurance Analyst
410000 Hoang Hoa
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Posted today
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Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and detail-oriented Remote Pharmaceutical Quality Assurance Analyst. This is a fully remote position where you will play a vital role in ensuring that our pharmaceutical products meet the highest standards of quality, safety, and efficacy. You will be responsible for developing, implementing, and maintaining quality assurance systems and procedures throughout the product lifecycle.
Key responsibilities include reviewing and approving batch records, investigating deviations and out-of-specification results, and managing change control processes. You will participate in internal and external audits, ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements (e.g., FDA, EMA), and contribute to the continuous improvement of quality systems. This role involves close collaboration with manufacturing, research and development, and regulatory affairs departments to address quality-related issues and implement corrective and preventive actions (CAPA).
The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 3-5 years of experience in quality assurance or quality control within the pharmaceutical industry is required. Strong knowledge of GMP guidelines, regulatory affairs, and quality management systems is essential. Excellent analytical, problem-solving, and documentation skills are crucial, along with meticulous attention to detail. The ability to work independently, manage multiple tasks efficiently, and communicate effectively with cross-functional teams in a remote setting is paramount. This opportunity is ideal for a QA professional looking to contribute their expertise to a reputable pharmaceutical organization while enjoying the flexibility of remote work.
Key responsibilities include reviewing and approving batch records, investigating deviations and out-of-specification results, and managing change control processes. You will participate in internal and external audits, ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements (e.g., FDA, EMA), and contribute to the continuous improvement of quality systems. This role involves close collaboration with manufacturing, research and development, and regulatory affairs departments to address quality-related issues and implement corrective and preventive actions (CAPA).
The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 3-5 years of experience in quality assurance or quality control within the pharmaceutical industry is required. Strong knowledge of GMP guidelines, regulatory affairs, and quality management systems is essential. Excellent analytical, problem-solving, and documentation skills are crucial, along with meticulous attention to detail. The ability to work independently, manage multiple tasks efficiently, and communicate effectively with cross-functional teams in a remote setting is paramount. This opportunity is ideal for a QA professional looking to contribute their expertise to a reputable pharmaceutical organization while enjoying the flexibility of remote work.
This advertiser has chosen not to accept applicants from your region.
4
Remote Pharmaceutical Quality Assurance Analyst
650000 Nha Trang, Khanh Hoa
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Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company, is searching for a meticulous and experienced Pharmaceutical Quality Assurance Analyst for a fully remote position. You will be responsible for ensuring that all pharmaceutical products and processes comply with stringent quality standards, regulatory requirements, and company policies. Your core duties will include reviewing batch records, developing and implementing quality control procedures, and participating in internal and external audits. You will also be involved in investigating deviations, CAPA (Corrective and Preventive Actions), and change control processes. A Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field is required. A Master's degree is advantageous. A minimum of 5 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry is essential. In-depth knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines (e.g., FDA, EMA) is mandatory. Excellent attention to detail, strong analytical and problem-solving skills, and proficient documentation abilities are crucial. The ability to work independently and manage multiple tasks in a remote setting is key. This is a significant opportunity to contribute to patient safety and product integrity from a remote work environment, playing a critical role in the pharmaceutical supply chain.
This advertiser has chosen not to accept applicants from your region.
5
Moderation Quality Assurance Analyst, Tiktok
Ho Chi Minh City
TikTok
Posted today
Job Viewed
Job Description
Responsibilities
About TikTok
TikTok is the leading destination for short-form mobile video. At TikTok, our mission is to inspire creativity and bring joy. TikTok's global headquarters are in Los Angeles and Singapore, and its offices include New York, London, Dublin, Paris, Berlin, Dubai, Jakarta, Seoul, and Tokyo.
Why Join Us
Creation is the core of TikTok's purpose. Our platform is built to help imaginations thrive. This is doubly true of the teams that make TikTok possible.
Together, we inspire creativity and bring joy - a mission we all believe in and aim towards achieving every day.
To us, every challenge, no matter how difficult, is an opportunity; to learn, to innovate, and to grow as one team. Status quo? Never. Courage? Always.
At TikTok, we create together and grow together. That's how we drive impact - for ourselves, our company, and the communities we serve.
Join us.
About
The e-commerce industry has seen tremendous growth in recent years and has become a hotly contested space amongst leading Internet companies, and its future growth cannot be underestimated. With millions of loyal users globally, we believe TikTok is an ideal platform to deliver a brand new and better e-commerce experience to our users. We aim to bring discovery, inspiration, and joy back to shopping by making TikTok the commerce channel of choice for merchants, creators, and affiliates.With millions of loyal users globally, we believe TikTok is an ideal platform to deliver a brand new and better e-commerce experience to our users. We are looking for passionate and talented people to join our product and operations team, to build an e-commerce ecosystem that is innovative, secure and intuitive for our users and brands.
**Responsibilities**:
Utilize quality management tools to strategically enhance policies through providing policy implementation feedback and minimizing moderation policy inefficiencies.
Develop quality assessment frameworks, map moderation rules and guidelines, and implement improvement plans to meet moderation quality metrics.
Collaborate with stakeholders (i.e. policy teams) and develop quality inspection standards, to continuously optimize & refine policies, processes and platforms.
Collaborate with BPO Quality Assurance Team to ensure a high quality standard of moderation delivery.
Work closely with QA market leaders, local partner operations, training & SOP teams to enhance moderation policies through identifying quality & product risks.
Validate and implement rejection labels, granting whitelist or revoking penalties stemming from erroneous human/machine moderation.
Initiate, lead & guide small/medium scale projects, pilot implementation of new platforms and tool functionalities aimed at enhancing moderation efficiency & quality.
Participate in large scale projects, aimed at identifying shortcomings or opportunities, provide business requirements (BRDs) from a moderation quality viewpoint.
**Qualifications**:
Minimum Qualifications
Bachelor's degree in any discipline.
Fluency in English and Vietnamese to moderate specific product/content listings for TikTok Shop Vietnam
Minimum 3 years of hands on and in-depth experience in e-commerce or online safety and quality analysis.
Excellent coordination skills and communication skills across multiple cross-functional teams to build plans and projects.
Support business in shifts by following the local labor laws.
Preferred Qualifications
Bachelor's Degree in business administration, operations, or project management.
Familiar with E-commerce compliance requirements and internet governance management, with a certain level of business sensitivity and risk awareness.
Able to digest large data sets/policies in a cohesive and actionable manner.
Experience in Program Management or Project Management roles.
TikTok is committed to creating an inclusive space where employees are valued for their skills, experiences, and unique perspectives. Our platform connects people from across the globe and so does our workplace. At TikTok, our mission is to inspire creativity and bring joy. To achieve that goal, we are committed to celebrating our diverse voices and to creating an environment that reflects the many communities we reach. We are passionate about this and hope you are too.
About TikTok
TikTok is the leading destination for short-form mobile video. At TikTok, our mission is to inspire creativity and bring joy. TikTok's global headquarters are in Los Angeles and Singapore, and its offices include New York, London, Dublin, Paris, Berlin, Dubai, Jakarta, Seoul, and Tokyo.
Why Join Us
Creation is the core of TikTok's purpose. Our platform is built to help imaginations thrive. This is doubly true of the teams that make TikTok possible.
Together, we inspire creativity and bring joy - a mission we all believe in and aim towards achieving every day.
To us, every challenge, no matter how difficult, is an opportunity; to learn, to innovate, and to grow as one team. Status quo? Never. Courage? Always.
At TikTok, we create together and grow together. That's how we drive impact - for ourselves, our company, and the communities we serve.
Join us.
About
The e-commerce industry has seen tremendous growth in recent years and has become a hotly contested space amongst leading Internet companies, and its future growth cannot be underestimated. With millions of loyal users globally, we believe TikTok is an ideal platform to deliver a brand new and better e-commerce experience to our users. We aim to bring discovery, inspiration, and joy back to shopping by making TikTok the commerce channel of choice for merchants, creators, and affiliates.With millions of loyal users globally, we believe TikTok is an ideal platform to deliver a brand new and better e-commerce experience to our users. We are looking for passionate and talented people to join our product and operations team, to build an e-commerce ecosystem that is innovative, secure and intuitive for our users and brands.
**Responsibilities**:
Utilize quality management tools to strategically enhance policies through providing policy implementation feedback and minimizing moderation policy inefficiencies.
Develop quality assessment frameworks, map moderation rules and guidelines, and implement improvement plans to meet moderation quality metrics.
Collaborate with stakeholders (i.e. policy teams) and develop quality inspection standards, to continuously optimize & refine policies, processes and platforms.
Collaborate with BPO Quality Assurance Team to ensure a high quality standard of moderation delivery.
Work closely with QA market leaders, local partner operations, training & SOP teams to enhance moderation policies through identifying quality & product risks.
Validate and implement rejection labels, granting whitelist or revoking penalties stemming from erroneous human/machine moderation.
Initiate, lead & guide small/medium scale projects, pilot implementation of new platforms and tool functionalities aimed at enhancing moderation efficiency & quality.
Participate in large scale projects, aimed at identifying shortcomings or opportunities, provide business requirements (BRDs) from a moderation quality viewpoint.
**Qualifications**:
Minimum Qualifications
Bachelor's degree in any discipline.
Fluency in English and Vietnamese to moderate specific product/content listings for TikTok Shop Vietnam
Minimum 3 years of hands on and in-depth experience in e-commerce or online safety and quality analysis.
Excellent coordination skills and communication skills across multiple cross-functional teams to build plans and projects.
Support business in shifts by following the local labor laws.
Preferred Qualifications
Bachelor's Degree in business administration, operations, or project management.
Familiar with E-commerce compliance requirements and internet governance management, with a certain level of business sensitivity and risk awareness.
Able to digest large data sets/policies in a cohesive and actionable manner.
Experience in Program Management or Project Management roles.
TikTok is committed to creating an inclusive space where employees are valued for their skills, experiences, and unique perspectives. Our platform connects people from across the globe and so does our workplace. At TikTok, our mission is to inspire creativity and bring joy. To achieve that goal, we are committed to celebrating our diverse voices and to creating an environment that reflects the many communities we reach. We are passionate about this and hope you are too.
This advertiser has chosen not to accept applicants from your region.
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6
Remote Senior Pharmaceutical Quality Assurance Analyst
49000 Thuy Van
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Posted today
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Our client is seeking a highly experienced Remote Senior Pharmaceutical Quality Assurance Analyst to join their advanced pharmaceutical research and development team. This is a fully remote role, requiring a meticulous professional with a deep understanding of pharmaceutical quality systems and regulatory compliance. You will be responsible for ensuring the quality and integrity of pharmaceutical products and processes by developing, implementing, and maintaining robust quality assurance programs. Your expertise will be vital in upholding the highest standards of safety and efficacy in drug development. Responsibilities:
- Develop, implement, and manage comprehensive Quality Assurance (QA) programs for pharmaceutical products.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines (e.g., FDA, EMA).
- Conduct thorough reviews of batch records, analytical data, and validation protocols.
- Investigate deviations, Out-of-Specification (OOS) results, and customer complaints, determining root causes and implementing corrective and preventive actions (CAPA).
- Perform internal audits and supplier audits to assess compliance with quality standards.
- Prepare and review Quality Management System (QMS) documentation, including SOPs, work instructions, and specifications.
- Collaborate with R&D, manufacturing, and regulatory affairs teams to ensure quality throughout the product lifecycle.
- Participate in regulatory inspections and audits by health authorities.
- Develop and deliver QA training programs for relevant personnel.
- Monitor key quality indicators and provide regular reports to management.
- Stay updated on changes in pharmaceutical regulations and industry best practices.
- Contribute to the continuous improvement of QA processes and systems.
- Manage validation activities for manufacturing processes, equipment, and analytical methods.
- Analyze quality trends and identify areas for process optimization.
- Maintain accurate and organized quality records.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 6-8 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- Strong knowledge of pharmaceutical manufacturing processes and regulatory requirements (GMP, ICH guidelines).
- Experience with quality risk management and root cause analysis methodologies.
- Excellent understanding of analytical techniques and validation principles.
- Proficiency in QMS software and document control systems.
- Exceptional attention to detail and accuracy.
- Strong written and verbal communication skills, with the ability to articulate complex quality issues.
- Proven ability to work independently and manage multiple tasks effectively in a remote setting.
- Experience in conducting audits and managing CAPA systems.
- Problem-solving and decision-making capabilities.
- Familiarity with pharmacovigilance principles is a plus.
This advertiser has chosen not to accept applicants from your region.
7
Senior Corporate Counsel - Regulatory Compliance
420000 Thai Binh , Thai Binh
WhatJobs
Posted 1 day ago
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Job Description
Our client is seeking a highly experienced Senior Corporate Counsel with a specialization in regulatory compliance to join their fully remote legal team. This pivotal role will focus on ensuring the company operates in full adherence to all applicable laws, regulations, and industry standards across its various business lines. The ideal candidate will possess a deep understanding of corporate law, risk management, and compliance frameworks, with a proven ability to navigate complex regulatory landscapes. You will be instrumental in developing and implementing robust compliance programs, conducting internal investigations, advising on risk mitigation strategies, and fostering a culture of compliance throughout the organization. This is a remote-first position, demanding exceptional self-discipline and strong digital collaboration skills. Responsibilities:
- Developing, implementing, and managing comprehensive corporate compliance programs.
- Monitoring changes in relevant laws and regulations and assessing their impact on the business.
- Advising on compliance matters related to data privacy, anti-corruption, competition law, and other areas.
- Conducting internal investigations into potential compliance violations and recommending corrective actions.
- Drafting and updating corporate policies, procedures, and codes of conduct.
- Providing training to employees on compliance-related topics.
- Liaising with regulatory authorities and managing governmental inquiries.
- Assessing and mitigating legal and compliance risks associated with new business initiatives.
- Staying abreast of best practices in corporate governance and compliance.
- Collaborating with internal stakeholders, including legal, finance, and operations departments.
- Supporting the General Counsel in overseeing the company's legal and compliance functions.
- Managing external counsel on specific compliance matters.
- Juris Doctor (JD) or equivalent law degree from a reputable university.
- Admission to practice law in Vietnam or a relevant jurisdiction.
- Minimum of 8 years of legal experience, with a significant focus on regulatory compliance, corporate governance, or related fields, preferably in-house or at a leading law firm.
- In-depth knowledge of relevant Vietnamese laws and regulations, as well as international compliance standards.
- Proven experience in developing and implementing compliance programs.
- Strong analytical, research, and problem-solving skills.
- Excellent written and verbal communication skills, with the ability to explain complex legal concepts clearly.
- Demonstrated ability to manage projects independently and work effectively in a remote setting.
- High level of integrity and ability to handle confidential information.
- Proficiency in English is required; knowledge of Vietnamese legal terminology is essential.
This advertiser has chosen not to accept applicants from your region.
8
Senior Aviation Regulatory Compliance Specialist
56000 An Thanh
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a globally recognized leader in the aviation industry, is looking for a highly experienced Senior Aviation Regulatory Compliance Specialist to join their fully remote team. In this critical role, you will be instrumental in ensuring that all operational activities and services comply with the complex and ever-evolving landscape of aviation regulations. You will conduct thorough reviews of policies, procedures, and operational data to identify any areas of non-compliance and develop strategic action plans to rectify them.
Your responsibilities will include interpreting aviation laws and regulations from various international bodies, advising management on compliance strategies, and overseeing the implementation of corrective actions. You will also be responsible for preparing and submitting regulatory documentation, liaising with aviation authorities, and staying abreast of regulatory changes. The ideal candidate will possess a deep understanding of aviation safety management systems (SMS), airworthiness directives, and operational certifications. Strong analytical skills, meticulous attention to detail, and the ability to communicate complex regulatory information clearly and concisely are paramount.
This is a remote-first position, providing the flexibility to work from anywhere while contributing to the company's global compliance efforts. You will utilize advanced digital collaboration tools and platforms to connect with internal teams and external stakeholders. A Bachelor's degree in Aviation Management, Law, or a related field, coupled with a minimum of 7 years of experience in aviation regulatory compliance, is essential. Professional certifications in aviation compliance or safety are highly desirable. This role requires a proactive approach to identifying and mitigating regulatory risks, ensuring our client's continued adherence to the highest standards of aviation safety and governance.
Your responsibilities will include interpreting aviation laws and regulations from various international bodies, advising management on compliance strategies, and overseeing the implementation of corrective actions. You will also be responsible for preparing and submitting regulatory documentation, liaising with aviation authorities, and staying abreast of regulatory changes. The ideal candidate will possess a deep understanding of aviation safety management systems (SMS), airworthiness directives, and operational certifications. Strong analytical skills, meticulous attention to detail, and the ability to communicate complex regulatory information clearly and concisely are paramount.
This is a remote-first position, providing the flexibility to work from anywhere while contributing to the company's global compliance efforts. You will utilize advanced digital collaboration tools and platforms to connect with internal teams and external stakeholders. A Bachelor's degree in Aviation Management, Law, or a related field, coupled with a minimum of 7 years of experience in aviation regulatory compliance, is essential. Professional certifications in aviation compliance or safety are highly desirable. This role requires a proactive approach to identifying and mitigating regulatory risks, ensuring our client's continued adherence to the highest standards of aviation safety and governance.
This advertiser has chosen not to accept applicants from your region.
9