Iso 42001 Compliance Manager Jobs

A World-Changing Company Palantir builds the world’s leading software for data-driven decisions and operations. By bringing the right data to the people who need it, our platforms empower our partners to develop lifesaving drugs, forecast supply chain disruptions, locate missing children, and more. The Role As a member of Palantir's Security Compliance team, you will develop a deep understanding of Palantir's control environment, infrastructure, and products. You will work with information security, business and product development experts, and external parties to navigate and manage commercial and international compliance frameworks (SOC/ISO 27001/17/18, ISO 9001) and geographically strategic compliance frameworks (ENS, TISAX, ISMAP, IRAP) in order to provide practical guidance on technical documentation, operational concerns, and sustainable processes that will allow us to continue to grow quickly & efficiently while also maintaining our current compliance obligations. You will additionally be a co-owner of our holistic internal risk management and internal control structures. We are looking for a team-focused and mission-oriented compliance professional that can navigate ambiguity and uncertainty, with the ability and desire to achieve goals and drive progress in an environment where outcomes must be achieved through their own resourcefulness and initiative. Core Responsibilities Assist in the performance of internal and external security assessments of Palantir products, infrastructure, and processes. Have a interest and general aptitude emerging technologies : from leveraging AI tooling, harnessing the capabilities of evidence automation and documentation management, and a general aptitude for agentic integration within workflows. Develop and maintain an understanding of Palantir’s control environment and articulate this understanding to various audiences, including internal and external stakeholders and auditors. Technica

A World-Changing Company Palantir builds the world’s leading software for data-driven decisions and operations. By bringing the right data to the people who need it, our platforms empower our partners to develop lifesaving drugs, forecast supply chain disruptions, locate missing children, and more. The Role As a member of Palantir's Security Compliance team, you will develop a deep understanding of Palantir's control environment, infrastructure, and products. You will work with information security, business and product development experts, and external parties to navigate and manage commercial and international compliance frameworks (SOC/ISO 27001/17/18, ISO 9001) and geographically strategic compliance frameworks (ENS, TISAX, ISMAP, IRAP) in order to provide practical guidance on technical documentation, operational concerns, and sustainable processes that will allow us to continue to grow quickly & efficiently while also maintaining our current compliance obligations. You will additionally be a co-owner of our holistic internal risk management and internal control structures. We are looking for a team-focused and mission-oriented compliance professional that can navigate ambiguity and uncertainty, with the ability and desire to achieve goals and drive progress in an environment where outcomes must be achieved through their own resourcefulness and initiative. Core Responsibilities Assist in the performance of internal and external security assessments of Palantir products, infrastructure, and processes. Have a interest and general aptitude emerging technologies : from leveraging AI tooling, harnessing the capabilities of evidence automation and documentation management, and a general aptitude for agentic integration within workflows. Develop and maintain an understanding of Palantir’s control environment and articulate this understanding to various audiences, including internal and external stakeholders and auditors. Technica

Should be innovative and should be able to give new ideas Should have good negotiation skills with vendors Conduct facility and EHS related trainings to the teams / vendors Ability to lead the team Should be able to quickly mobilize resources to meet the ever changing demands Should be able to coordinate with the building authorities for building related matters Reporting to the client on daily and weekly basis Work closely with finance to ensure vendors are paid on time 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 Attendance Weekly & monthly reports Consumable Report and Incident Report & Clients Meeting Tracker. Handling employee s queries and resolving them in a professional manner. Ensure all operational and safety procedures are properly followed. Inspect and approve staff work performance. Demonstrate leadership and training to staff. Communicate effectively to staff. Should have knowledge in HT/LT panels DG LV & ELV systems UP HVAC Fire hydrant & FAS BMS UPS WTP STP and RO system Solar system. Prepare the reports for Preventive and Predictive maintenance MTTR&MTBR Energy management new improvements & sustainability activities. Responsible for legal documents & follow-ups CAPX& OPAX budget preparation Spare management. Address: Mr.Rajeshkumar,C/O, Alstom transport India Limited, SF No. 41/1BA, 41/2A, Kangeyampalayam, Village, Sulur Taluk, Coimbatore Facility: ALSTOM TRANSPORT - COIMBATORE Qualification: Graduate Experience: 5 - 10 years Source: Sodexo India | Job Code: IJP577164

Job Title Backend Sales Support Engineer Job Type: Full-time Location: Nashik Experience: Experience 1 to 4 year Salary -2.50 to 3.50 lacs Job description We Monk Automation Private Limited are manufacturer of automation control panels and channel partner of Schneider Electric leading brands in automation products,We have urgent requirement for Sales Engineer. ROLES AND Responsibilities: Identifying the customer’s current and future requirements. Demonstrating products, services and solutions to potential clients. Reviewing customer drawings, plans and other documents in order to prepare detailed technical proposal for them. Negotiating Offers, payment terms and delivery. Prepare report for attending sales review meeting on regular period. Achieving Payment collection Awareness about the product. Prepared tenders, and proposals documents. Making daily, weekly and monthly reports. Good knowledge of ERP software. Maintain documents as per ISO . Maintain documents as per KPI . Background · At least 1 4years of experience in Sales and Marketing in Nashik in Automation / Electrical Panel Industry BE/BTech Engineering Electrical, Electronics or instrumentation engineer,Electrical and Telecommunication/ Instrumentation/ Robotics& Automation Background in acquisition of small to large order, estimation and offer preparation Knowledge of, PLC, Drives, switchgear, MCC, PCC, SCADA, Control Panel Has good decision-making capability Bond: - 2 Lacs of amount for 3 Years is mandatory. Candidate those who are ready to work in bond can only apply.

MEDICAL CODING Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT and HCPCS. ELIGIBILITY Any Bio or Life Science, Medical, Paramedical, Dental, Pharmacy, physiotherapy, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Botony, Zoology, Bioinformatics, BAMS, BHMS, BSMS, BNYS, BUMS, BEMS, Nutrition & Dietetics, Plant Biology, Advance Zoology HIGHLIGHTS OF NESTEM TECHNOLOGIES ISO 9001:2015 Certified and Govt Registered Institution Presentation and Video Classes by well Experienced Certified Trainers Complete Anatomy, Physiology and Pathology Training Complete Medical Coding (ICD-10 CM, CPT-4 & HCPCS) Training Complete Coverage of Industrial Requirement Flexible Class Timings, Placements with Certification High End Study Materials Software's for Practice, Free Communication, Technical & Attitude Classes PLACEMENTS & PAY DETAILS FOR TRAINED After successful completion of the Training job offer will be provided in Leading MNC's. Placements will be in Chennai, Vellore, Trichy, Coimbotore, Salem, Pune, Bangalore & Hyderabad. 12700/- to 14800/- PM initially with assured career growth (Excluding Special Allowances & Other Benefits). DIRECT PLACEMENT ONLY IN CHENNAI *We provide direct placement for those having well knowledge in Human Anatomy & Physiology at FREE OF COST. This assistance will be given at our specific MNC Client in Chennai. For further Information Call us on 979 1196 983 / 044-2481 4757.

MEDICAL CODING Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT and HCPCS. ELIGIBILITY UG / PG in Life Science, Medical, Paramedical, Bio-Computing, Medical Socialogy COURSE OFFERED FOR FRESHERS 1. Medical Coding For Beginners (MCB) 2. Advance certification in Medical Coding (ACMC) HIGHLIGHTS OF NESTEM TECHNOLOGIES ISO 9001:2015 Certified and Govt Registered Institution Presentation and Video Classes by well Experienced Certified Trainers Complete Anatomy, Physiology and Pathology Training Complete Medical Coding (ICD-10 CM, CPT-4 & HCPCS) Training Complete Coverage of Industrial Requirement Flexible Class Timings, Placements with Certification High End Study Materials Software's for Practice, Free Communication, Technical & Attitude Classes 1) MEDICAL CODING FOR BEGINNERS (MCB) Nestem Technologies provides 90 Hours of Training in Certification in Medical Coding for Beginners(Charges Applicable). The following modules will be covered in the Certification in Medical Coding for Beginners. 2) ADVANCED CERTIFICATION IN MEDICAL CODING (ACMC) Nestem Technologies provides 120 Hours of Training in Advanced Certification in Medical Coding (Charges Applicable). The following Additional Modules will be covered in Advanced Certification in Medical Coding PLACEMENTS & PAY DETAILS FOR TRAINED After successful completion of the Training job offer will be provided in Leading MNC's. Placements will be in Chennai, Vellore, Trichy, Coimbatore, Salem, Tirunelveli, Viluppuram Initial Net Salary will be 13650/-. DIRECT PLACEMENT ONLY IN CHENNAI *We provide direct placement for those having well knowledge in Human Anatomy & Physiology at FREE OF COST. This assistance will be given at our specific MNC Client in Chennai. For further Information Call us on 860 8291 818

Role Description Responsible for maintaining and continuously improving the Efficiency and profitability of the assigned operation whilst Maintaining a high standard of service in accordance with Budget Key Responsibilities Should be innovative and should be able to give new ideas Should have good negotiation skills with vendors Conduct facility and EHS related trainings to the teams / vendors Ability to lead the team Should be able to quickly mobilize resources to meet the ever changing demands Should be able to coordinate with the building authorities for building related matters Reporting to the client on daily and weekly basis Work closely with finance to ensure vendors are paid on time 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 Attendance Consumable Report and Incident Report & Clients Meeting Tracker. Handling employee s queries and resolving them in a professional manner. Ensure all operational and safety procedures are properly followed. Inspect and approve staff work performance. Demonstrate leadership and training to staff. Communicate effectively to staff. Qualification Should be having an experience of 4 10years with Facility Management background. Should possess an eye for detail The person needs to have excellent communication skills experience in working with a very young and demanding set of employees having the ability to navigate in unknown circumstances and situations and needs to connect well with the employees. A very smart energetic person who is capable of taking initiative and decisions when needed. Address: Plot 255 & 238 Part of Survey 151 Dholera Village Dholera SIR Ahmedabad Gujarat Facility: Tata Semicon

Work Flexibility: Hybrid What You Will Do / Roles & Responsibilities As a member of the Global Product Engineering team you will gain in depth knowledge about Stryker’s Trauma & Extremities portfolio. You will learn how Bone Plates & Screws, External Fixators, Surgical Instruments and many other products improve people’s life. Together we are responsible for over 50'000 articles. We count on you to maintain and improve our high standard in design specification and performance. You ensure compliance with applicable regulatory and quality requirements, including FDA, EU MDR, ISO 13485, and internal standards, by driving design change management activities, support regulatory submissions, and serving as a subject matter expert during internal and external audits. In your field of responsibility, you will make sure that design requirements are met as well as apply the design change process and identify technical solutions in this context. You oversee the continuous improvement projects for existing products in our group, create and manage project plans, assign and follow up on work packages. You participate in and at times lead cross functional teams to perform design related Non-Conformities(NC), Corrective- and Preventive-Actions(CAPA). Your role will include frequent contact with other teams such as the international Regulatory Affairs, Tech. Publications, Design Quality or Marketing to address design related questions for international registrations and creations of technical files required for the implementation of EU-MDR requirements. Drive value improvement, design optimization, and continuous improvement initiatives to enhance product performance, quality, compliance, and cost effectiveness. What You Need <

Locum Blood Transfusion Biomedical Scientist Banding: Band 6 Location: Leeds Rate: £23–£27 per hour, with additional shift uplifts Start date: ASAP Duration: Ongoing Working pattern: Long days, 3 days on / 3 days off, with rotating night shifts An exciting opportunity has arisen for an experienced Blood Transfusion Biomedical Scientist to join a well-established NHS laboratory in Leeds. This is an excellent opportunity to work within a newly built, cutting-edge blood sciences laboratory , providing Blood Transfusion services in a modern NHS laboratory environment. The role offers an ongoing assignment with a long-day rotational shift pattern and additional uplifts for applicable shifts. What will your responsibilities be? Perform routine and specialist Blood Transfusion testing in line with departmental SOPs. Undertake group and screen testing, antibody investigations and crossmatching where required. Carry out quality control, result validation and troubleshooting. Support safe and effective transfusion practice. Maintain compliance with UKAS accreditation, ISO 15189 standards and local laboratory policies. Work confidently and independently across long-day and night shifts. Collaborate with biomedical, clinical and support colleagues to deliver an efficient diagnostic service. Qualifications and Experience HCPC registration as a Biomedical Scientist. BSc Biomedical Science or equivalent recognised qualification. Relevant post-registration experience in Blood Transfusion. Experience working within a busy diagnostic laboratory. Knowledge of transfusion quality requirements. Ability to work independently and as part of a wider laboratory team. Why work with Pulse? From the moment you register with us, our focus is entirely on you. Our expert recruitment consultants are dedicated to finding you the best opportunities and supporting you every step of the way to secure the right placement. With preferred or sole supplier status with many clients, you’ll have access to e

Senior Biomedical Scientist – Histopathology & Dissection - Relocation and Signing on Bonus Location: Oxfordshire Salary: £60,000 to £65,000 per annum, depending on experience Contract: Permanent Start Date: ASAP Hours: 37.5 hours per week, including rotational weekend working On-call: None Benefits: £10,000 relocation allowance | £10,000 sign-on bonus | 25 days’ annual leave, increasing annually to 30 days Take the next step in your Histopathology career An exciting permanent opportunity has arisen for an experienced Senior Biomedical Scientist specialising in Histopathology and Dissection to join a growing private laboratory in Oxfordshire. This is an excellent opportunity for an accomplished Biomedical Scientist who has built substantial experience in a busy diagnostic environment and is now looking for a role where their specialist dissection and cut-up expertise will be highly valued. You’ll be joining during an exciting period of permanent expansion, becoming part of an ambitious laboratory environment where experienced scientists play an important role in delivering a high-quality diagnostic service. What will your responsibilities be? Dissection will be a major focus of this position. You’ll use your senior histopathology expertise across the specimen pathway while supporting the quality and efficiency of the wider laboratory service. Undertake histology specimen dissection and cut-up within your demonstrated competencies and professional scope of practice. Work with a range of histology specimens, including biopsies and larger specimens where appropriately trained and authorised. Contribute across the histopathology workflow, including embedding, microtomy, special stains, IHC support and slide quality control where required. Maintain accurate specimen documentation, macroscopic descriptions, block selection and LIMS records. Contribute to turnaround-time delivery, quality assurance and audit readiness. Work in accordance with UKAS accreditation, ISO 15

JOB DESCRIPTION: Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to: • Career development with an international company where you can grow the career you dream of. • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. In Abbott's Medical Devices Divisions We are dedicated to advancing healthcare through innovative medical technologies that improve patient outcomes and transform lives. Our Medical Devices portfolio supports healthcare professionals worldwide with cutting-edge solutions across Cardiac Rhythm Management, Electrophysiology, Heart Failure, Neuromodulation, and Structural Heart therapies. The Opportunity QA Specialist This role will support the commercial Quality Assurance and Regulatory Compliance (QARC) activities across the EMEA region, based in Solihul, ensuring compliance with quality management systems, ISO standards, and medical device regulations. The successful candidate will work closely with affiliates, third-party logistics providers, distributors, and cross-functional teams to maintain high-quality warehousing, inventory, and distribution processes. Wha

Work Flexibility: Onsite It's Time to Join Stryker! Join Stryker's Mako Robotics team as a Senior Product Safety Engineer, helping ensure the safety, reliability, and regulatory compliance of advanced robotic-assisted surgical technologies. In this hands-on engineering role, you will partner closely with electrical, systems, and cross-functional engineering teams to identify and mitigate product safety risks throughout development. You will support electrical safety and electromagnetic compatibility (EMC) testing, troubleshoot technical challenges, and help ensure products meet applicable industry standards. This opportunity is ideal for an engineer with a strong electrical foundation who enjoys practical problem-solving, laboratory testing, and collaborating with design teams to develop safe, high-quality medical devices. What You Will Do Product Safety & Risk Management: Identify, evaluate, and document electrical and system-level safety hazards. Develop and maintain risk management documentation, including hazard analyses, FMEAs, and safety assessments, while recommending practical risk mitigation strategies. Electrical Safety & EMC: Apply electrical safety and electromagnetic compatibility principles to evaluate product designs, identify potential compliance concerns, and support troubleshooting and design improvements. Standards & Compliance: Interpret and apply relevant medical device safety standards, with particular emphasis on IEC 60601 and its relationship to ISO 14971 and applicable regulatory requirements. Testing & Laboratory Coordination: Plan, coordinate, and support electrical safety and EMC testing with internal teams and external laboratories, including UL, CSA, TÜV, and other recognized testing organizations. Prepare test

JOB DESCRIPTION: 【岗位职责】 1. 遵循标准操作程序&#xff08;SOP&#xff09;和工作说明&#xff0c;使用手动和电动工具、有限的自动化设备、制造辅助工具/固定装置、升降机/起重机和制造过程中的其他方法进行布线、组件安装、电缆线束、装配仪器的安装等。仪器装配员是一个渐进式角色&#xff0c;随着经验提升会学习到更多组件、流程和精度组件的装配。 2. 检查和验证组件和成品的质量&#xff0c;以确保它们符合规范并符合法规要求&#xff0c;例如 FDA 指南和 ISO 标准。 3. 排除故障并解决生产问题或差异。与其他部门合作&#xff0c;如工程、质量、卓越业务和产品开发&#xff0c;提供有关产品设计、可制造性、工艺改进的反馈。还与工程师、质量保证和生产主管等跨职能团队合作&#xff0c;以确保生产流程顺畅 4. 准确及时地记录和记录生产活动&#xff0c;包括装配过程、产品信息、关键零件的材料控制、标签活动和质量不合格。 5. 遵守公司政策、程序和法规&#xff0c;包括质量管理体系&#xff08;QMS&#xff09;&#xff0c;并有助于维护质量、合规性和持续改进的文化。 6. 遵循良好生产规范&#xff08;GMP&#xff09;&#xff0c;并遵守安全法规&#xff0c;以确保安全和高效的工作环境。 7. 凭借久经考验的效率和能力&#xff0c;可能需要这个角色来培训其他装配人员。具体工作职能可能会发生变化。需要执行分配的其他职责。 【任职资格】 1. 资格证书/Certificate&#xff1a; 有钳工证优先 2. 外语技能/Foreign Language Skills&#xff1a; 有大学英语四级证书优先 3. 计算机软件技能Software Skills&#xff1a; </spa

The following description is not intended as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Management retains the discretion of adding or changing the duties of the position at any time. SUMMARY The Quality Control Director develops, implements, and periodically evaluates the Company’s program to ensure the organizations production operations, from raw materials to finished products, meet the quality, integrity, and efficiency standards set by the Company. JOB DESCRIPTION Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Strategic Leadership and Quality System Oversight: Develop and implement comprehensive quality strategies and programs across multiple locations, ensuring alignment with corporate goals. Lead quality assurance teams, providing direction and support to ensure consistency and compliance with all quality standards. Quality Systems Management: Establish and maintain all required certifications and upholding all relevant standards (including ISO 9001) Oversee the management and enhancement of all quality systems and processes, including quality control, quality assurance, and quality improvement. Oversee the design, implementation, and maintenance of robust quality assurance processes and procedures. Work closely with engineering, operations, R&D, and procurement to develop incoming material specifications and requirements that optimize our manufacturing processes. Lead MRB activities, provide guidance with customer MRB requirements and assist with in-process and supplier corrective actions. Establish robust supplier quality program include assessments, qualifications, and ongoing monitoring of key suppliers. Problem-solving and Critical Thinking: Apply advanced problem-solving skills and critical thinking to identify root causes of issues and implement strategic solutions that result in systemic improvements. Champion initiativ

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. Job Summary: We are looking for an experienced Senior Mechanical Engineer to oversee design review, execution, and commissioning of HVAC systems and Process Utility systems for large-scale Oil & Gas and Pharmaceutical projects. The role involves end-to-end project management, including stakeholder coordination (PMC, GC, and sub-vendors), ensuring compliance with international standards, and delivering projects safely, on time, and within budget. Key Responsibilities: • Supervise and review the work of GC, PMC, and sub-vendors to ensure compliance with contractual obligations and project specifications. • Conduct regular site inspections and escalate any deviations, delays, or quality issues to the client management team. • Review engineering deliverables such as P&IDs, PFDs, equipment sizing calculations, data sheets, and technical specifications. • Validate designs for compliance with API, ASME, ASTM, ISO, IS codes, ASHRAE, SMACNA, and cGMP guidelines. • Ensure accurate integration of HVAC and Process Utility systems into project scope. • Review vendor documents, GA drawings, and layout for correctness and constructability. • Plan and supervise execution activities for HVAC and Process Utility systems across multiple work fronts. • Coordinate with PMC, General Contractors, and sub-vendors for timely execution and issue resolution. • Drive construction sequencing, resource allocation, and contractor mobilization plans. • Prepare and m