safety compliance specialist

Guildhall

The Role
 We are currently seeking a Labelling & Compliance Specialist for a company in the food and confectionery industry based in Al Quoz, Dubai. This newly created position focuses on ensuring product labelling and documentation meet UAE and GCC regulatory standards as the company continues to expand its product range across the region. * Manage and ensure product label compliance with UAE and GCC municipality requirements. * Prepare and maintain documentation for product registration and approvals. * Liaise with authorities and third-party labs for certification and label verification. * Coordinate with suppliers and designers to ensure correct ingredient and allergen declarations. * Keep updated with changes in GCC labelling and food safety regulations and communicate them internally. * Additional tasks related to municipality approvals, product registration, or other similar regulatory responsibilities may also be assigned as needed.
 
Requirements
 <ul>
<li>Strong knowledge of food labelling standards and documentation procedures in GCC countries. * Proficient in English (Arabic is an advantage). * Detail-oriented, organized, and able to manage multiple product lines. * Excellent communication and coordination skills.</li>
</ul>
About the company
 Guildhall is the most respected HR & Headhunting Consultancy in the MENA Region. With deep, extensive knowledge of HR & Recruiting in the region, Guildhall has become a trusted partner of choice for candidates and clients. Starting from an exclusive recruitment agency in Dubai - UAE, Guildhall has grown into an elite service with the ability to cover vacancies in across MENA and Asia-pacific. Offering tailored Career Sessions and an innovative industry-first membership program designed to save money on core services. Guildhall is the partner of choice.

Labelling And Compliance Specialist

Virtu Thinko

Role Summary: The Compliance &amp; Risk Specialist ensures all cloud and security operations meet relevant regulatory standards and internal governance requirements.Key Responsibilities:<ul><li>Map cloud security controls to regulatory frameworks (PDPL, PCI DSS, ISO 27001, etc.).</li><li>Maintain documentation for audits and certifications.</li><li>Conduct regular compliance checks and risk assessments.</li><li>Prepare reports for management and regulators.</li><li>Support awareness training and policy development.</li></ul>Qualifications &amp; Skills:<ul><li>Bachelor&rsquo;s degree in Risk Management, IT, or related discipline.</li><li>5+ years of experience in compliance or cybersecurity governance.</li><li>Knowledge of GCC regulatory frameworks (CBB, SAMA, CBUAE).</li><li>Strong analytical and documentation skills.</li><li>Preferred certifications: ISO 27001 Lead Implementer, CRISC, CISA.</li></ul>Job Types: Full-time, Contract Contract length: 12 monthsPay: BD1,000.000 - BD2,000.000 per month

Compliance & Risk Specialist

Syneos Health

<div>
 
 Description
 
 
 
 Safety &amp; PV Specialist II (Literature Review)
 
 
 Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
 
 
 Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
 
 
 Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
 
 
 Discover what our 29,000 employees, across 110 countries already know:
 
 
 
 WORK HERE MATTERS EVERYWHERE
 
 
 
 Why Syneos Health
 
 
 <ul>
 <li>
 We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
 </li>
 <li>
 We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
 </li>
 <li>
 We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.
 
 
 </li>
 </ul>
 
 Job Responsibilities
 
 
 
 
 JOB RESPONSIBILITIES
 
 
 
 <ul>
 <li>
 Conduct systematic and ad-hoc literature searches in global biomedical databases (e.g., Embase, PubMed, Medline) for ICSR identification and safety-relevant information.
 </li>
 <li>
 Skilled in extracting and summarizing key safety information from identified literature sources
 </li>
 <li>
 Thorough understanding of creating and validating search strategies for pharmacovigilance purpose.
 </li>
 <li>
 In depth knowledge of major literature databases such as Embase, PubMed etc.
 </li>
 <li>
 Experience in conducting local literature searches and reviews.
 </li>
 <li>
 Understanding of regulatory requirements with respect to global and local literature.
 </li>
 <li>
 Enters information into PVG quality and tracking systems for receipt and tracking ICSR.
 </li>
 <li>
 May assist in the preparation of the Safety Management Plan
 </li>
 <li>
 Processes ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans.
 </li>
 <li>
 Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability.
 </li>
 <li>
 Enters data into safety database.
 </li>
 <li>
 Codes events, medical history, concomitant medications and tests.
 </li>
 <li>
 Compiles complete narrative summaries.
 </li>
 <li>
 Assesses information to be queried and follows up until information is obtained and queries are satisfactorily resolved.
 </li>
 <li>
 Participates in the generation of timely, consistent and accurate reporting of expedited reports in accordance with applicable regulatory requirements.
 </li>
 <li>
 Coordinates with data management staff concerning reconciliation of safety data between the clinical and safety databases.
 </li>
 <li>
 Ensures distribution of all required individual expedited and periodic reports for both clinical and post-marketing projects to the Safety Submissions team if contracted to submit the reports.
 </li>
 <li>
 Participate in audits/inspections as required
 </li>
 <li>
 Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate.
 </li>
 <li>
 Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCPs, ICH guidelines, GVP, project/program plans and the drug development process.
 
 
 </li>
 </ul>
 Good communication and interpersonal skills, both written and spoken
 
 
 Bachelor&rsquo;s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job.
 
 
 
 What We&rsquo;re Looking For
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree, Postgraduate in health profession with relevant experience, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job.
 </li>
 <li>
 At least 3+ years of experience in Pharmacovigilance, Literature case reviewing (Global+Local), Identifying NICR (Signal &amp; AR) report from Literature.
 </li>
 <li>
 Mandatory to have GVP Module 6 knowledge
 </li>
 <li>
 Safety Database systems and knowledge of medical terminology required
 </li>
 <li>
 Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance
 </li>
 <li>
 Proficiency in Microsoft Office Suite (Word, Excel and PowerPoint), Visio, email (Outlook), TeamShare (or other management/shared content/workspace) and internet.
 </li>
 <li>
 Ability to work independently and in a team environment
 </li>
 <li>
 Good communication and interpersonal skills, both written and spoken
 </li>
 <li>
 Good organizational skills with proven ability to prioritize and work on multiple tasks and projects
 </li>
 <li>
 Detail oriented with a high degree of accuracy and ability to meet deadlines
 </li>
 <li>
 Minimal travel may be required (up to 5%)
 
 
 </li>
 </ul>
 
 Get to know Syneos Health
 
 
 
 Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
 
 
 No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
 
 
 http://www.syneoshealth.com
 
 
 
 Additional Information
 
 
 
 Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
 
 
 
 Summary
 
 
 
 Performs all aspects of the collection, processing, and reporting of individual cases safety reports (ICSR), adhering to all data privacy guidelines, Good Clinical Practices (GCPs), Good Pharmacovigilance Practice (GVP), regulatory guidelines, company and project/program-specific procedures for clinical trials and/or post-marketing safety programs.
</div>

Safety & PV Specialist II (Literature Review)

<div>Description
Safety &amp; PV Specialist II (Literature Review)
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health<ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul>
Job Responsibilities
JOB RESPONSIBILITIES
<ul><li>Conduct systematic and ad-hoc literature searches in global biomedical databases (e.g., Embase, PubMed, Medline) for ICSR identification and safety-relevant information.</li><li>Skilled in extracting and summarizing key safety information from identified literature sources</li><li>Thorough understanding of creating and validating search strategies for pharmacovigilance purpose.</li><li>In depth knowledge of major literature databases such as Embase, PubMed etc.</li><li>Experience in conducting local literature searches and reviews.</li><li>Understanding of regulatory requirements with respect to global and local literature.</li><li>Enters information into PVG quality and tracking systems for receipt and tracking ICSR.</li><li>May assist in the preparation of the Safety Management Plan</li><li>Processes ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans.</li></ul>
o Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. 
o Enters data into safety database. 
o Codes events, medical history, concomitant medications and tests. 
o Compiles complete narrative summaries. 
o Assesses information to be queried and follows up until information is obtained and queries are satisfactorily resolved. 
o Participates in the generation of timely, consistent and accurate reporting of expedited reports in accordance with applicable regulatory requirements. 
o Coordinates with data management staff concerning reconciliation of safety data between the clinical and safety databases. 
<ul><li>Ensures distribution of all required individual expedited and periodic reports for both clinical and post-marketing projects to the Safety Submissions team if contracted to submit the reports.</li><li>Participate in audits/inspections as required</li><li>Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate.</li><li>Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCPs, ICH guidelines, GVP, project/program plans and the drug development process.</li></ul>
 Good communication and interpersonal skills, both written and spoken 
 Bachelor&rsquo;s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job.
What we&rsquo;re looking for<div><ul><li> 
Bachelor&rsquo;s Degree, Postgraduate in health profession with relevant experience, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills and abilities to perform the job.</li></ul></div><ul><li>At least 3+ years of experience in Pharmacovigilance, Literature case reviewing (Global+Local), Identifying NICR (Signal &amp; AR) report from Literature.</li><li>Mandatory to have GVP Module 6 knowledge
</li><li>Safety Database systems and knowledge of medical terminology required</li><li>Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance</li><li>Proficiency in Microsoft Office Suite (Word, Excel and PowerPoint), Visio, email (Outlook), TeamShare (or other management/shared content/workspace) and internet.</li><li>Ability to work independently and in a team environment</li><li>Good communication and interpersonal skills, both written and spoken</li><li>Good organizational skills with proven ability to prioritize and work on multiple tasks and projects</li><li>Detail oriented with a high degree of accuracy and ability to meet deadlines</li><li>Minimal travel may be required (up to 5%)</li></ul>
Get to know Syneos Health 
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information 
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Performs all aspects of the collection, processing, and reporting of individual cases safety reports (ICSR), adhering to all data privacy guidelines, Good Clinical Practices (GCPs), Good Pharmacovigilance Practice (GVP), regulatory guidelines, company and project/program-specific procedures for clinical trials and/or post-marketing safety programs.</div>

Tether Operations Limited

<div>Join Tether and Shape the Future of Digital Finance
At Tether, we&rsquo;re not just building products, we&rsquo;re pioneering a global financial revolution. Our cutting-edge solutions empower businesses&mdash;from exchanges and wallets to payment processors and ATMs&mdash;to seamlessly integrate reserve-backed tokens across blockchains. By harnessing the power of blockchain technology, Tether enables you to store, send, and receive digital tokens instantly, securely, and globally, all at a fraction of the cost. Transparency is the bedrock of everything we do, ensuring trust in every transaction.
Innovate with Tether
Tether Finance: Our innovative product suite features the world&rsquo;s most trusted stablecoin, USDT, relied upon by hundreds of millions worldwide, alongside pioneering digital asset tokenization services.
But that&rsquo;s just the beginning:
Tether Power: Driving sustainable growth, our energy solutions optimize excess power for Bitcoin mining using eco-friendly practices in state-of-the-art, geo-diverse facilities.
Tether Data: Fueling breakthroughs in AI and peer-to-peer technology, we reduce infrastructure costs and enhance global communications with cutting-edge solutions like KEET, our flagship app that redefines secure and private data sharing.
Tether Education: Democratizing access to top-tier digital learning, we empower individuals to thrive in the digital and gig economies, driving global growth and opportunity.
Tether Evolution: At the intersection of technology and human potential, we are pushing the boundaries of what is possible, crafting a future where innovation and human capabilities merge in powerful, unprecedented ways.
Why Join Us?
Our team is a global talent powerhouse, working remotely from every corner of the world. If you&rsquo;re passionate about making a mark in the fintech space, this is your opportunity to collaborate with some of the brightest minds, pushing boundaries and setting new standards. We&rsquo;ve grown fast, stayed lean, and secured our place as a leader in the industry.
If you have excellent English communication skills and are ready to contribute to the most innovative platform on the planet, Tether is the place for you.
Are you ready to be part of the future?
About the job
The Senior Compliance Specialist will lead the implementation and monitoring of the company&rsquo;s compliance framework across key conduct and regulatory domains, including Conflicts of Interest, Anti-Bribery &amp; Corruption, Fraud, Market Abuse, Data Protection, Outsourcing, and Ethics.
This position plays a strategic role in embedding a culture of integrity, managing cross-border compliance risks, and ensuring adherence to global regulatory expectations.
Responsibilities<ul><li>
Regulatory Oversight: Implement and maintain compliance policies and controls related to conduct risk, ABC, CoI, fraud, data protection, market abuse, and outsourcing.</li><li>
Advisory: Advise management and business units on ethical practices, conflicts management, and third-party risk compliance.</li><li>
Monitoring &amp; Assurance: Perform periodic compliance risk assessments, thematic reviews, and control testing programs.</li><li>
Incident Management: Oversee investigations into potential misconduct, conflicts, or regulatory breaches, ensuring timely remediation and escalation.</li><li>
Training &amp; Culture: Design and deliver conduct risk and ethics training across all business units.</li><li>
Data Protection: Support in ensuring compliance with the applicable data protection regimes.</li><li>
Governance &amp; Reporting: Prepare reports for the Board and regulators summarizing compliance findings, trends, and remediation progress.</li><li>
Regulatory Change Management: Monitor new regulations and ethical standards and ensure timely implementation.</li></ul>
Mentorship: Supervise junior compliance staff, ensuring consistency in compliance monitoring and advisory work.<ul><li> 
Education: Bachelor&rsquo;s degree in Law, Business, Finance or a related discipline.</li><li>
Experience: 3-5 years of experience in regulatory compliance, conduct risk, or ethics programs within financial services.</li><li>
Certifications: ICA, CFE, CAFS, CCAS, CCEP-I, CIPP/E, CFCS, or equivalent preferred.</li><li>
Proven expertise in managing compliance frameworks for CoI, ABC, FRM, and outsourcing.</li><li>
Excellent analytical, investigative, and communication skills with the ability to translate regulatory requirements into operational controls.</li><li>
Fluency in English is required; proficiency in an additional language is highly preferred.</li></ul>
Important information for candidates 
Recruitment scams have become increasingly common. To protect yourself, please keep the following in mind when applying for roles:<ul><li>
Apply only through our official channels. We do not use third-party platforms or agencies for recruitment unless clearly stated. All open roles are listed on our official careers page: https://tether.recruitee.com/</li><li>
Verify the recruiter&rsquo;s identity. All our recruiters have verified LinkedIn profiles. If you&rsquo;re unsure, you can confirm their identity by checking their profile or contacting us through our website.</li><li>
Be cautious of unusual communication methods. We do not conduct interviews over WhatsApp, Telegram, or SMS. All communication is done through official company emails and platforms.</li><li>
Double-check email addresses. All communication from us will come from emails ending in @tether.to or @tether.io</li><li>
We will never request payment or financial details. If someone asks for personal financial information or payment at any point during the hiring process, it is a scam. Please report it immediately.</li></ul>
When in doubt, feel free to reach out through our official website.</div>

Senior Regulatory Compliance Specialist (Non-AML) - 100% remote

[24]7.ai

<div>
 
 Position : Security &amp; Compliance Specialist
 
 
 Reports to: Manager InfoSec, GRC
 
 
 Department: Information Security (InfoSec)
 
 
 Location: Bangalore
 
 
 Work Mode : Hybrid
 
 
 
 
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 
 
 
 This role oversee the development, evaluation and implementation of governance, risk and compliance.
 
 
 
 
 
 This role provides operational and conformance checking of information security implemented. The role will undertake specific audits tasks directly and will work with identified stakeholders to ensure that audit lifecycle is in compliance.
 
 
 
 
 
 Additionally, this role will undertake regular conformance checking tasks to ensure compliance is met to acceptable security levels in different audits.
 
 
 
 
 
 This role will also undertake a number of critical asks and requests from security projects which manages to successful delivery of projects and the associated resources.
 
 
 
 
 
 Further, this role will work with all departments across Technology, Business and Third Party vendors/partners and manages inter-dependencies / work-streams and across multiple projects to ensure that Projects are delivered on time:
 
 
 
 
 <ul>
 <li>
 Provide consulting services for Technology &amp; Business team for Audit Security process and implementation of controls.
 </li>
 <li>
 Define Security assessment scope, requirements, time lines and goals.
 </li>
 <li>
 Pro-actively reviews all gaps found on audits related to systems and types of access controls on various risks like Cyber Threats, Data Security and compliance and communicate for timely actions to mitigate them.
 </li>
 <li>
 Supports in managing all type of internal and external InfoSec audits (end to end), status of Security assessment, Report Observations and remediation with all the agreed timelines.
 </li>
 <li>
 Works with end customer SPOC to ensure all the desired requirements are delivered by liaising with all the business stakeholders.
 </li>
 <li>
 Delivers Security Assessments projects on time, and at the expected quality, have root- cause analysis with clear action plan and obtain sign-off with all relevant parties.
 </li>
 </ul>
 
 
 
 
 
 
 Preferred Skills
 
 
 
 <ul>
 <li>
 Ensure the organization complies with local, federal and international regulatory and legal requirements
 </li>
 <li>
 Stay up to date on all major privacy and data protection laws, GDPR, CCPA, DPA, PIPEDA etc.
 </li>
 <li>
 Experience in handling various Security Assessments, regulatory requirements but not limited to PCI- DSS, ISO27001, ISO9001, GDPR, CCPA, SOC2 and privacy shield.
 </li>
 <li>
 Practical understanding of security standards, Processes and risk frameworks.
 </li>
 <li>
 Has good understanding of audit frameworks and various datasheet involved in preparing for the external audits.
 </li>
 <li>
 Knowledge of current industry best practices and standards, local/international security and compliance guidance.
 </li>
 <li>
 Broad, and commensurately high-level knowledge of Security technology, such as: PKI, firewalls, access management, encryption, IDS &amp; IPS, Cyber threats, encryption, and identity management.
 </li>
 <li>
 Strong time management, communication and prioritization skills.
 </li>
 <li>
 Ability to work with Technical and Non- Technical business owners.
 </li>
 <li>
 Practical understanding of security processes and risk frameworks.
 </li>
 <li>
 Partners with External consultants/ internal stakeholders on Regulatory Changes to ensure regulatory changes are added within the system of record.
 </li>
 <li>
 Drive integration with Compliance teams aligned to Business Units for all the related audits (end to end).
 </li>
 <li>
 Knowledge of current industry best practices and standards, local/international security and compliance guidance.
 </li>
 <li>
 Conducting deep dives into specific areas of focus based on Risk and Regulatory priorities as and when needed.
 </li>
 <li>
 Proficiency in reviewing and assessing process flows to detect potential risks, deficient controls, duplicated effort, extravagance, and fraud, non-compliance with laws, regulations, and management policies.
 </li>
 <li>
 Partners with other Operations Managers to ensure timely and effective delivery for all audit requirements.
 </li>
 <li>
 Contribute to the Group ISMS content development, maintenance and maturity.
 </li>
 <li>
 Take the interface between custom authorities and colleagues/partners on customs Audits.
 </li>
 <li>
 Drive matrixed project planning and execution to deliver and sustain privacy compliance
 </li>
 </ul>
 
 
 
 Required Qualifications
 
 
 
 <ul>
 <li>
 Bachelor/Master of Science degree. Computer Science, Engineering, Telecommunications or management degree(would be advantage)
 </li>
 <li>
 6/6+ years&rsquo; experience in audits and compliance management
 </li>
 <li>
 Excellent planning, multi-tasking, organization and problem solving skills.
 </li>
 <li>
 Knowledge of certifications and framework like NIST, HIPAA, ISO 27K, PCI-DSS and SOC2.
 </li>
 <li>
 Excellent communication skills.
 </li>
 <li>
 Hold certifications like ISO9001, ISO 27001 and Green belt(added advantage)
 </li>
 </ul>
 
 
</div>

Security & Compliance Specialist

Search 10000+ Safety compliance specialist jobs near you this November. New roles added regularly across leading industries. Apply today.

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Senior Regulatory Compliance Specialist (Non-AML) - 100% remote

Security & Compliance Specialist