Iso 42001 Compliance Manager Jobs

Datadog is seeking a Payroll Specialist to keep up with our rapidly growing company. As a Payroll Specialist, you will support the US payroll process for over 3000 employees. Direct responsibilities will include facilitating the semi monthly payroll for salaried exempt and nonexempt employees. The Payroll Specialist will review accuracy and partner closely with senior team leads to ensure payrolls are processed in a timely fashion. You will also be responsible for providing administrative support across our Canada, and Latin America population. Most importantly, you will collaborate with our People and Finance teams to continue to scale this important function. At Datadog, we place value in our office culture - the relationships and collaboration it builds and the creativity it brings to the table. We operate as a hybrid workplace to ensure our Datadogs can create a work-life harmony that best fits them. What You’ll Do Partner with payroll team stakeholders to analyze data entry feeds while also supporting the semi-monthly payroll process from start to finish, ensuring employees are paid correctly and on time within our Workday payroll module. Understand the US payroll function and process payroll according to internal accounting principals and regulatory requirements. Process new hires, terminations, status changes, tax changes, domestic and international transfers, 401k contribution feeds and changes, timesheet data, compensation changes, employee personal information changes, retroactive adjustments, garnishments and supplemental payments entered into Workday HRIS. Resolve payroll discrepancies by running and analyzing Workday data reports. Directly involved in processing of equity transactions inclusive of restricted stock units (RSU), non-qualified stock options (NSO), incentive stock options (ISO), disqualified dispositions and all other equity related transactions. Collaborate with Finance stakeholders to support audits, identify and

To lead and manage Quality Assurance activities of the PMR Laboratory by ensuring accurate and timely analysis of raw materials, in-process samples, finished products, and precious metal assays while maintaining compliance with ISO 17025, NABL requirements, IMS standards, safety regulations, data integrity requirements, and business turnaround commitments. The role shall drive laboratory excellence, analytical reliability, operational efficiency, method development, team capability building, and continuous improvement initiatives. Source: Adani Group | Job ID: 54176

Consultant Histopathologist Consultant Histopathologist Our client is seeking an experienced and motivated Consultant Histopathologist to join their well-established pathology service. This is an excellent opportunity to join a progressive department that combines a supportive working culture with modern laboratory facilities and a strong commitment to service development, education and research. The successful candidate will contribute to the department's general histopathology workload while also having the opportunity to develop specialist interests that complement the existing consultant team. This position would suit both newly qualified consultants approaching CCT and experienced Histopathologists looking for their next substantive appointment. The Opportunity Working within an experienced multidisciplinary team, the successful applicant will play an important role in delivering a comprehensive diagnostic histopathology service while contributing to the continued development of pathology services across the organisation. The laboratory is fully accredited to UKAS ISO 15189:2022 standards and benefits from modern facilities, contemporary diagnostic equipment and an established mortuary service operating under a Human Tissue Authority (HTA) licence . The department undertakes a substantial post-mortem workload alongside a broad range of routine and specialist histopathology services, providing excellent opportunities for consultants wishing to maintain and develop a varied practice. Key Responsibilities The successful applicant will be expected to: Deliver a high-quality diagnostic histopathology service. Participate in the department's general reporting workload. Develop a specialist area of practice alongside existing consultant expertise. Work collaboratively with consultant colleagues and multidisciplinary clinical teams. Provide professional leadership and support to scientific, technical and medical staff. Participate in departmental governance, audi

Standort: Frankfurt, Düsseldorf, Berlin, München (Hybrid) | Practice Area : Banking & Payments | Anstellungsart: Unbefristet Gestalte mit uns die Zukunft des Zahlungsverkehrs – von SEPA-Prozessen und ISO-20022-Nachrichten bis hin zu modernen, AI-gestützten Arbeitsweisen. Die Rolle Als (Senior) Consultant* – SEPA Payments begleitest Du anspruchsvolle Beratungsprojekte im Zahlungsverkehr und unterstützt unsere Kunden entlang des gesamten Projektzyklus – von der Business Analyse und Fachkonzeption über das Testing bis hin zur Implementierung. Dabei bringst Du Deine Payments-Expertise ein und nutzt geeignete, freigegebene AI-Tools und AI-gestützte Workflows, um Analysen, Qualität und Produktivität zu verbessern – stets mit menschlicher Beurteilung und unter Berücksichtigung geltender Responsible-AI-Leitplanken. Mit zunehmender Projekterfahrung übernimmst Du mehr Verantwortung für Deine Themen bis hin zur Leitung von Teilprojekten und kleineren Projektteams. Deine Aufgaben Du begleitest anspruchsvolle Beratungsprojekte im Zahlungsverkehr von der Business Analyse und Fachkonzeption über das Testing bis hin zur engen Begleitung der Implementierung. Du arbeitest kundenorientiert und bringst Deine eigenen Erfahrungen sowie die Expertise Deiner Capco-Kolleg*innen wirkungsvoll in die Projektarbeit ein. Du analysierst fachliche Anforderungen und Payments-Prozesse und entwickelst gemeinsam mit unseren Kunden tragfähige Lösungen. Du übernimmst zunehmend Verantwortung für Deine Themen bis hin zur Leitung von Teilprojekten und kleineren Projektteams. Du nutzt freigegebene AI-Tools, Automatisierung und AI-gestützte Workflows dort, wo sie einen praktischen Mehrwert für Geschwindigkeit, Qualität oder Erkenntnisgewinn bieten, und stellst durch Review, menschliche Beurteilung und definierte Eskalationswege eine verantwortungsvolle Nutzung sicher. Dein Profil Du hast ein großes Interesse an (SEPA-)Payments und möchtest Deine Kenntnisse in diesem hochaktuellen Themenfeld einbringen un

Should be innovative and should be able to give new ideas Should have good negotiation skills with vendors Ability to lead the team Should be able to quickly mobilize resources to meet the demands Should be able to coordinate with the site authorities for site related matters Reporting to the F.M on daily and weekly basis Conducting compliance audits and ISO audits on behalf of clients. Able to lead guide and motivate for Entry level & Middle level staff. Maintaining relationship with quality vendors that they are reliable and cost effective. Make Daily Reports of Deployment Log book Inventory etc.. Handling employee s queries and resolving them in a professional manner. Ensure all operational and safety procedures are properly followed. Inspect staff work performance. Demonstrate leadership and training to staff. Communicate effectively to staff. Qualification Should be having an experience of 1 4years with Facility Management background. Should possess an eye for detail The person needs to have good communication skills experience in working with diverse set of employees having the ability to navigate in unknown circumstances and situations and needs to connect well with the employees. A person who is capable of taking initiative when needed Address: Nahars Amrit Shakti Road, Chandivali Farm Road, off, Saki Vihar Rd, Andheri East, Mumbai, Maharashtra Facility: NAHAR INTERNATIONAL SCHOOL Qualification: 12th Experience: 1 - 5 years Source: Sodexo India | Job Code: IJP576081

Figma is growing our team of passionate creatives and builders on a mission to make design accessible to all. Figma’s platform helps teams bring ideas to life—whether you're brainstorming, creating a prototype, translating designs into code, or iterating with AI. From idea to product, Figma empowers teams to streamline workflows, move faster, and work together in real time from anywhere in the world. If you're excited to shape the future of design and collaboration, join us! As a Compliance Engineer at Figma, you will play a critical role in designing, implementing, and testing security controls across multiple compliance frameworks, including FedRAMP, SOC 2, ISO 27001, and NIST. You will collaborate closely with security, infrastructure, and product engineering teams to translate regulatory requirements into effective technical controls, evaluate control effectiveness, and identify opportunities to improve security and compliance processes. You will also help advance Figma’s compliance engineering capabilities by leveraging automation, machine-readable control definitions (JSON), APIs, and AI-assisted development tools to streamline control testing, evidence collection, and continuous monitoring. This role combines deep security compliance expertise with technical problem-solving to build scalable, repeatable, and effective compliance practices. This is a full time role that can be held from one of our US hubs or remotely in the United States. What you’ll do at Figma: Develop and verify technical security controls that satisfy multiple compliance frameworks Collaborate with security, infrastructure, and product engineering teams to translate compliance requirements into effective technical controls Design and execute control testing procedures to assess control performance, surface gaps, and verify that remediation is complete Establish repeatable control assessments and continuous monitoring processes to evaluate compliance effectiveness Translate security require

Job Title: Band 6 Biomedical Scientist – Biochemistry Banding: Band 6 Location: Surrey Rate: £22 - £26 per hour Start Date: ASAP Duration: Ongoing Working Hours: Full-time, including out-of-hours shifts, weekends, and Bank Holidays An exciting opportunity has arisen for an experienced Band 6 Biomedical Scientist to join a well-established NHS laboratory in Surrey. This role offers the chance to work within a busy Clinical Biochemistry service, supporting the delivery of high-quality diagnostic testing in a modern laboratory environment. What will your responsibilities be: • Perform routine and specialist Clinical Biochemistry investigations in accordance with departmental policies and procedures • Operate, maintain, and troubleshoot automated biochemistry analysers • Validate and authorise results within the scope of competency and laboratory protocols • Ensure accurate and timely processing of samples to support patient care • Participate in quality control, quality assurance, and audit activities • Maintain compliance with UKAS, ISO 15189, and departmental standards • Support service delivery across the department and contribute to continuous improvement initiatives • Participate in the laboratory's out-of-hours rota, including evenings, weekends, and Bank Holidays Qualifications and Experience: Essential: • HCPC registration as a Biomedical Scientist • Previous experience working within a Clinical Biochemistry laboratory • Competency using Abbott Alinity analysers and/or laboratory information management systems (LIMS) • Strong understanding of quality assurance and laboratory governance processes • Excellent organisational skills and the ability to prioritise workload effectively Desirable: • Previous Band 6 experience within Clinical Biochemistry • Experience working in a high-throughput NHS laboratory environment • Experience participating in an out-of-hours service rota Why work with Pulse? From the moment you registe

Here’s a summary of the role: Every enterprise deal reaches the moment where someone in security says “prove it.” You’re the person who answers — quickly, accurately, and with the evidence to back it up. As an Analyst II on our Trust & Assurance team, you’ll own a live queue of security questionnaires, third-party due diligence assessments, RFP security sections and customer assurance requests. You’ll draft at speed using AI-assisted response tooling, then verify every answer against our approved answer library, current SOC 2 and ISO 27001 certifications and the underlying evidence before it leaves your hands. Accuracy is the whole game here: a wrong answer in a customer questionnaire is a commitment we didn’t mean to make. The best part is that you won’t just work the queue — you’ll shrink it. Every recurring question you turn into a published answer on our trust site is a ticket that never comes back. If you’ve spent two to four years in security GRC, compliance, IT audit or customer assurance, you’re precise under volume, and you like being measured on turnaround time and first-pass accuracy, you’ll do well here. Here’s a breakdown of what you’ll do (not all of it, just the important stuff): Own a high-volume queue of security questionnaires, due diligence assessments, RFP security sections and assurance requests, delivering accurate responses within SLA. Use AI-assisted response tooling to draft at speed, then verify every answer against the approved answer library, current certifications and underlying evidence before it goes out. Triage and route incoming requests using established playbooks — resolving the routine independently and escalating anything novel, contractual or architecturally complex. Maintain and expand the answer library by adding approved answers, retiring stale ones and flagging inconsistencies, so the same question never has to be researched twice. Build out trust site and customer-facing content, and show commercial teams how to

For over 20 years, Smartsheet has empowered teams to manage work seamlessly and scale solutions smarter. Now, in our most ambitious chapter yet, we are uniting human teams with AI agents. By orchestrating the work agents do best, automating manual tasks and uncovering insights at scale, we create the space for people to focus on what truly matters: judgment, creativity, and big thinking. That is magic at work, and it’s what we show up for every day. Smartsheet maintains certifications and attestations across SOC 2 Type II, the ISO 27001/27017/27701/22301 suite, HIPAA, and other commercial compliance frameworks—and the manual work of proving those controls quarter after quarter doesn't scale with the business. We're looking for a Sr. Security Engineer I to bring an engineering mindset to our commercial GRC program: automating control monitoring, building evidence pipelines, and reducing the audit-season scramble into a default state of readiness. You'll work hands-on with our GRC platform, cloud, and identity tooling to make control evidence collect itself wherever possible, and you'll partner closely with engineering teams to translate compliance requirements into technical control logic they can actually build against. This is a builder's role within GRC—less checklist administration, more systems thinking applied to compliance. Our approach is grounded in GRC Engineering principles: automate early and often, treat controls and their mappings as code, favor continuous assurance over periodic checks, and build compliance that engineers can consume as easily as they contribute to it. This role reports to the Senior Director, GRC Engineering and can be based in our Bellevue, WA office or remotely from anywhere in the US where Smartsheet is a registered employer. You Will: Own control automation for SOC 2, ISO 27001/27017/27701, HIPAA, and related commercial frameworks: design and build automated evidence collection and continuous control monitoring across cloud, ident

Job Title: Biomedical Scientist – Microbiology (Bacteriology) Banding: Band 6 Location: Central England Start date: ASAP Working hours: Full-time An exciting opportunity has arisen for an experienced Band 6 Biomedical Scientist to join a well-established laboratory in Central England on a locum basis. This role offers the chance to work within a busy Microbiology department, supporting the delivery of high-quality diagnostic services with a particular focus on Bacteriology. What will your responsibilities be: • Perform a range of routine and specialist Microbiology investigations within a Bacteriology laboratory. • Process, analyse, interpret, and report microbiological samples in accordance with departmental procedures. • Operate and maintain laboratory equipment while ensuring quality standards are consistently met. • Participate in the day-to-day running of the laboratory and support efficient workflow management. • Maintain accurate records and ensure compliance with UKAS, ISO 15189, and laboratory quality standards. • Work collaboratively with multidisciplinary teams to support patient care and service delivery. • Adhere to all health and safety, infection prevention, and laboratory governance policies. Qualifications and Experience: Essential • HCPC registration as a Biomedical Scientist. • Previous experience working as a Band 6 Biomedical Scientist in a UK Microbiology laboratory. • Strong Bacteriology knowledge and practical laboratory experience. • Ability to work independently within a busy diagnostic environment. • Excellent communication and organisational skills. Desirable • Experience using laboratory information management systems (LIMS). • Experience working within an NHS laboratory setting. • Knowledge of quality management systems and accreditation requirements. Why work with Pulse? From the moment you register with us, our focus is entirely on you. During our first conversation, you'll quickly see that we understand your spec

Job Title: Locum Biomedical Scientist – Blood Transfusion Banding: Band 6 or 7 equivalent Location: Edinburgh Rate: £33 - £39 per hour DOE Start date: ASAP Duration: Ongoing Working hours: All shift patterns available An exciting opportunity has arisen for an experienced Biomedical Scientist specialising in Blood Transfusion to join a modern and well-equipped private laboratory in Edinburgh. This role is suited to a Band 6 or Band 7 professional with strong transfusion experience and hands-on expertise using Grifols analysers, looking to work within a high-performing laboratory team on a flexible shift basis. What will your responsibilities be: • Perform routine and specialist Blood Transfusion testing in accordance with laboratory procedures and quality standards • Operate, maintain and troubleshoot Grifols analysers to ensure accurate and timely test results • Undertake blood grouping, antibody screening, compatibility testing and blood issue activities • Participate in all shift patterns, including days, nights, weekends and bank holidays where required • Ensure compliance with UKAS, ISO 15189 and laboratory quality requirements • Accurately record and authorise results using laboratory information management systems (LIMS) • Investigate and resolve transfusion-related queries and non-conformances where appropriate • Contribute to quality assurance, audit activities and service improvement initiatives • Work collaboratively with multidisciplinary teams to support the delivery of high-quality patient care Qualifications and Experience: • HCPC registration as a Biomedical Scientist • Previous NHS or private sector Blood Transfusion laboratory experience • Extensive experience using Grifols analysers is essential • Experience working at Band 6 or Band 7 level within a Blood Transfusion laboratory • Strong understanding of Blood Transfusion policies, procedures and best practice • Familiarity with UKAS accreditation and ISO 15189 standards • Exce

Banding: Band 4-6 Location: East Midlands Rate: £18-£27 per hour (depending on banding and experience) Start Date: ASAP Duration: 3-6 months Working Hours: Monday-Friday, Core Hours An exciting opportunity has arisen for a Histology professional to join a well-established NHS laboratory in the East Midlands. This locum position is ideal for an experienced candidate looking to support a busy Cellular Pathology service, contributing to the delivery of high-quality diagnostic results and patient care. What will your responsibilities be: Support the processing of histology specimens within a busy Cellular Pathology laboratory. Perform embedding, microtomy, staining, and associated laboratory procedures appropriate to experience and banding. Assist with specimen preparation, quality control procedures, and maintenance of laboratory standards. Ensure compliance with UKAS accreditation, ISO 15189 requirements, and departmental SOPs. Accurately record and manage laboratory data using relevant laboratory information systems. Work collaboratively with biomedical scientists, pathologists, and laboratory support staff to maintain an efficient service. Qualifications and Experience: Relevant laboratory experience within Histology/Cellular Pathology. Previous NHS laboratory experience is highly desirable. Experience in microtomy, embedding, staining, and specimen preparation appropriate to banding level. Good understanding of laboratory quality standards and health and safety requirements. Experience using laboratory information management systems (LIMS) is advantageous. Ability to work independently and as part of a multidisciplinary laboratory team. Why work with Pulse? From the moment you register with us, our focus is entirely on you. During our first conversation, you'll quickly see that we understand your specialty inside and out. Our expert recruitment consultants are dedicated to finding you the best opportunities and supporting you every step of the way to secure the rig

Locum Blood Transfusion Biomedical Scientist Banding: Band 6 Location: West Yorkshire Rate: £20-£27 per hour Start Date: ASAP Duration: 3-6 Months Working Pattern: Rotational shifts comprising 3 long days followed by a block of 3 night shifts An exciting opportunity has arisen for a Biomedical Scientist to join a well-established NHS laboratory in West Yorkshire. This locum role is ideal for an experienced Blood Transfusion professional who can support a busy transfusion service, deliver accurate results, and contribute to safe, effective patient care. What will your responsibilities be: Perform routine and specialist Blood Transfusion testing in line with departmental SOPs. Support safe transfusion practice, including group and screen testing, antibody investigations, compatibility testing, and crossmatching. Carry out analyser maintenance, quality control, result validation, and troubleshooting activities. Maintain compliance with UKAS accreditation, ISO 15189 standards, and local laboratory policies. Work collaboratively with biomedical, clinical, and support staff to ensure the delivery of a high-quality transfusion service. Participate in the department's rotational shift pattern, covering both long day and night shifts. Qualifications and Experience: Essential HCPC registration as a Biomedical Scientist. BSc Biomedical Science or equivalent recognised qualification. Post-registration experience working within a UK Blood Transfusion laboratory. Experience performing group and screen, crossmatching, and antibody investigations. Familiarity with laboratory information systems and transfusion quality requirements. Ability to work independently and as part of a wider laboratory team. Desirable Previous NHS Blood Transfusion experience at Band 6 level. Knowledge of UKAS accreditation and ISO 15189 standards. Experience working a 24/7 transfusion rota. Why work with Pulse? From the moment you register with us, our focus is entirely on you. During our first conversati

Our vision is to transform how the world uses information to enrich life for all . Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever. The Program Manager for Quality Assurance / Quality Control will lead the development, deployment, and governance of construction quality management across Micron’s U.S. semiconductor fab expansion. This role is responsible for establishing field-executable quality procedures aligned to corporate standards, ISO 9001 principles, and applicable industry codes, ensuring consistent, measurable, and compliant project delivery in support of semiconductor construction, including clean build protocols and phased system turnover. You will implement structured processes, performance metrics, and oversight mechanisms that integrate quality requirements across all phases of project execution—from planning through turnover. Through program governance, contractor engagement, and continuous improvement, you will drive quality performance, compliance, and predictable outcomes. This role serves as a primary interface between program leadership, and site teams ensuring alignment of quality expectations, and effective implementation of QA/QC plan. Responsibilities Lead QA/QC program governance, establishing standards, processes, and controls to ensure consistent execution across projects. Develop and maintain Quality Management Plans aligned to corporate standards, regulatory requirements, and lifecycle delivery. Define and enforce quality requirements in contracts and execution plans, ensuring alignment across contractors, EPCs, and third-party providers. Establish and monitor quality performance metrics, includin

Here’s a summary of the role: Every enterprise deal reaches the moment where someone in security says “prove it.” You’re the person who answers — quickly, accurately, and with the evidence to back it up. As an Analyst II on our Trust & Assurance team, you’ll own a live queue of security questionnaires, third-party due diligence assessments, RFP security sections and customer assurance requests. You’ll draft at speed using AI-assisted response tooling, then verify every answer against our approved answer library, current SOC 2 and ISO 27001 certifications and the underlying evidence before it leaves your hands. Accuracy is the whole game here: a wrong answer in a customer questionnaire is a commitment we didn’t mean to make. The best part is that you won’t just work the queue — you’ll shrink it. Every recurring question you turn into a published answer on our trust site is a ticket that never comes back. If you’ve spent two to four years in security GRC, compliance, IT audit or customer assurance, you’re precise under volume, and you like being measured on turnaround time and first-pass accuracy, you’ll do well here. Here’s a breakdown of what you’ll do (not all of it, just the important stuff): Own a high-volume queue of security questionnaires, due diligence assessments, RFP security sections and assurance requests, delivering accurate responses within SLA. Use AI-assisted response tooling to draft at speed, then verify every answer against the approved answer library, current certifications and underlying evidence before it goes out. Triage and route incoming requests using established playbooks — resolving the routine independently and escalating anything novel, contractual or architecturally complex. Maintain and expand the answer library by adding approved answers, retiring stale ones and flagging inconsistencies, so the same question never has to be researched twice. Build out trust site and customer-facing content, and show commercial teams how to