79 Regulatory Compliance jobs in India

Manager, Financial Crime and Compliance-1

Gurugram, Uttar Pradesh TaskUs

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Job Description

About TaskUs: TaskUs is a provider of outsourced digital services and next-generation customer experience to fast-growing technology companies, helping its clients represent, protect and grow their brands. Leveraging a cloud-based infrastructure, TaskUs serves clients in the fastest-growing sectors, including social media, e-commerce, gaming, streaming media, food delivery, ride-sharing, HiTech, FinTech, and HealthTech. 

The People First culture at TaskUs has enabled the company to expand its workforce to approximately 45,000 employees globally.Presently, we have a presence in twenty-three locations across twelve countries, which include the Philippines, India, and the United States.

It started with one ridiculously good idea to create a different breed of Business Processing Outsourcing (BPO)! We at TaskUs understand that achieving growth for our partners requires a culture of constant motion, exploring new technologies, being ready to handle any challenge at a moment’s notice, and mastering consistency in an ever-changing world.

What We Offer: At TaskUs, we prioritize our employees' well-being by offering competitive industry salaries and comprehensive benefits packages. Our commitment to a People First culture is reflected in the various departments we have established, including Total Rewards, Wellness, HR, and Diversity. We take pride in our inclusive environment and positive impact on the community. Moreover, we actively encourage internal mobility and professional growth at all stages of an employee's career within TaskUs. Join our team today and experience firsthand our dedication to supporting People First.

Key Responsibilities

  • Develop and implement Fraud and Risk Management practices that are in line with the client’s needs and regulatory frameworks

  • Identify digital tools in the Fraud space to meet with specific client requirements

  • Work closely with the operations & support teams to identify potential risks

  • Identify the need and methods to automate fraud detection and risk mitigation as per client’s requirements

  • You will need to research and develop market insights and industry best practices in fraud detection and risk management

  • Participate inthe presales process including but not limited to RFP/RFI responses, Point of View management and overall deal solutioning

  • Participate in client discussions to craft pro-active solutions to meet client needs

  • Demonstrate in-depth knowledge on Fraud Detection, Investigation, Dispute management and other related practices. 

  • Provide thought leadership and detailed execution on diverse projects

  • Identify areas of risk and make recommendations on operational improvements, quality assurance and any additional training crucial to mitigate risk. Seeks ways to assist the organization in strengthening the FCRM practice

  • Identify transformation needs and opportunities and facilitate client discussions for execution

  • Requirements:

  • Graduate in any field (CFE & CAMS certified preferred)

  • 6+ experience in Customer Lifecycle Management, Fraud Investigations or disputes and chargeback management

  • Someone with a solid understanding and experience on Anti-fraud practices. 

  • Understand the latest tools and technologies prevalent in the space and has experience in building/contributing in designing digital tools (using RPA, ML, run queries and build macros)

  • Experience in Client Management.

  • Good analytical and problem-solving skills and ability to handle team and client discussions

  • Bachelor’s degree or a combination of education and experience. 

  • How We Partner To Protect You: TaskUs will neither solicit money from you during your application process nor require any form of payment in order to proceed with your application. Kindly ensure that you are always in communication with only authorized recruiters of TaskUs.


    DEI: In TaskUs we believe that innovation and higher performance are brought by people from all walks of life. We welcome applicants of different backgrounds, demographics, and circumstances. Inclusive and equitable practices are our responsibility as a business. TaskUs is committed to providing equal access to opportunities. If you need reasonable accommodations in any part of the hiring process, please let us know.

    We invite you to explore all TaskUs career opportunities and apply through the provided URL.

    This advertiser has chosen not to accept applicants from your region.

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    Regulatory Compliance

    Mumbai, Maharashtra Abbott

    Posted 17 days ago

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    Job Description

    **Primary** **Job** **Function:**
    To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations. The role is critical to maintaining business continuity and regulatory compliance.
    **Core Job Responsibilities:**
    **Regulatory Submissions and compliance**
    + Prepare and submit various applications such as additional product permission, Layout approval, facility modification approval, technical person approval, Test license, amendments in licenses, State GMP and GLP certificate applications, post approval changes etc. to State FDA
    + Prepare and submit applications such as Test license NOC, WHO GMP applications, CPP applications for additional products.
    + Ensure timely submissions and approvals for all regulatory filings.
    + Evaluate technical and scientific data for regulatory submissions.
    + Liaise with health authorities for inspections, clarifications, and approvals.
    + Ensure compliance with D&C Act, NDPS Act, Gazette Notifications, and internal SOPs.
    **Product & Business Support**
    + Handle product complaints from regulatory authorities, coordinating with QA, Legal, SCM, and Manufacturing for resolution.
    + Provide regulatory support for internalization and externalization of products.
    + To provide site CMC documents to international business team to support export registration.
    **Documentation & Quality Oversight**
    + Maintain and update regulatory databases, trackers, licenses, and approvals.
    + Review and track regulatory impact of quality documents such as change controls, deviations, FLQRs, and product certifications.
    + Evaluate and approve site change controls and Change Request evaluation forms.
    + Provide working standards/specifications and CoAs to regulatory authorities and internal teams.
    **Tender Certificates**
    + To obtain NCC, Manufacturing & Marketing Certificates, and CMC documents to support institutional and international business.
    + Coordinate with Institutional business team and site team for documentation as well as to facilitate site inspection of tendering authority.
    **Governance, SOPs & Training**
    + Support the preparation, revision, and implementation of Regulatory SOPs and work instructions.
    + Deliver training on GMP, regulatory updates, and SOPs at the site level.
    + Approve SCNs from Corporate QA and review reports from regulatory authorities.
    **Additional Responsibilities**
    + Complete assigned trainings on time
    + Perform other duties as assigned by the Regulatory Affairs leadership.
    + Act as the regulatory lead for the site, ensuring alignment with corporate and regulatory expectations.
    **Position Accountability/Scope:**
    + ·Responsible for all regulatory activities for the manufacturing site mainly LL sites.
    + ·Ensures site compliance with applicable national regulations and Abbott standards.
    + Supports business continuity through proactive regulatory planning and execution.
    **Minimum Education:**
    B.Pharm / M.Pharm / M.Sc. or equivalent in pharmaceutical or life sciences discipline.
    **Minimum Experience/Training Required:**
    + **Manager:** Minimum 08 - 12 years of experience in Regulatory Affairs preferably with a multinational or leading Indian pharmaceutical company. Prior experience in Quality Assurance is desirable.
    + Familiarity with regulatory platforms (SUGAM, ONDLS, NSWS, SolTRAQs) is desirable.
    An Equal Opportunity Employer
    Abbot welcomes and encourages diversity in our workforce.
    We provide reasonable accommodation to qualified individuals with disabilities.
    To request accommodation, please call or email
    This advertiser has chosen not to accept applicants from your region.

    Regulatory Compliance

    Mumbai, Maharashtra Abbott

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    Primary Job Function:

    To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations. The role is critical to maintaining business continuity and regulatory compliance.

    Core Job Responsibilities:

    Regulatory Submissions and compliance
  • Prepare and submit various applications such as additional product permission, Layout approval, facility modification approval, technical person approval, Test license, amendments in licenses, State GMP and GLP certificate applications, post approval changes etc. to State FDA
  • Prepare and submit applications such as Test license NOC, WHO GMP applications, CPP applications for additional products.
  • Ensure timely submissions and approvals for all regulatory filings.
  • Evaluate technical and scientific data for regulatory submissions.
  • Liaise with health authorities for inspections, clarifications, and approvals.
  • Ensure compliance with D&C Act, NDPS Act, Gazette Notifications, and internal SOPs.
  • Product & Business Support
  • Handle product complaints from regulatory authorities, coordinating with QA, Legal, SCM, and Manufacturing for resolution.
  • Provide regulatory support for internalization and externalization of products.
  • To provide site CMC documents to international business team to support export registration.
  • Documentation & Quality Oversight
  • Maintain and update regulatory databases, trackers, licenses, and approvals.
  • Review and track regulatory impact of quality documents such as change controls, deviations, FLQRs, and product certifications.
  • Evaluate and approve site change controls and Change Request evaluation forms.
  • Provide working standards/specifications and CoAs to regulatory authorities and internal teams.
  • Tender Certificates
  • To obtain NCC, Manufacturing & Marketing Certificates, and CMC documents to support institutional and international business.
  • Coordinate with Institutional business team and site team for documentation as well as to facilitate site inspection of tendering authority.
  • Governance, SOPs & Training
  • Support the preparation, revision, and implementation of Regulatory SOPs and work instructions.
  • Deliver training on GMP, regulatory updates, and SOPs at the site level.
  • Approve SCNs from Corporate QA and review reports from regulatory authorities.
  • Additional Responsibilities
  • Complete assigned trainings on time
  • Perform other duties as assigned by the Regulatory Affairs leadership.
  • Act as the regulatory lead for the site, ensuring alignment with corporate and regulatory expectations.
  • Position Accountability/Scope:

  • ·Responsible for all regulatory activities for the manufacturing site mainly LL sites.
  • ·Ensures site compliance with applicable national regulations and Abbott standards.
  • Supports business continuity through proactive regulatory planning and execution.
  • Minimum Education:

    B.Pharm / M.Pharm / M.Sc. or equivalent in pharmaceutical or life sciences discipline.

    Minimum Experience/Training Required:

  • Manager: Minimum 08 – 12 years of experience in Regulatory Affairs preferably with a multinational or leading Indian pharmaceutical company. Prior experience in Quality Assurance is desirable.
  • Familiarity with regulatory platforms (SUGAM, ONDLS, NSWS, SolTRAQs) is desirable.
  • This advertiser has chosen not to accept applicants from your region.

    RC-REGULATORY COMPLIANCE-REGULATORY COMPLIANCE-Manager

    Kolkata, West Bengal EY

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    The opportunity

    We’re looking for Manager with expertise in Computer System Validation and Stakeholder Management to join the leadership group of our EY-Regulatory Compliance team. This is a fantastic opportunity to be part of a leading firm whilst being instrumental in the growth of emerging service offering.

    Your key responsibilities

  • Actively contribute to the IT applications project management initiatives that includes Validation activities as per GAMP Life Cycle approach
  • Integrate technology with business process transformation programs like SAP, LIMS, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc.
  • Perform Gap assessment and Remediation procedures for legacy applications to ensure validation policies is in line with Life Cycle Approach
  • Perform Software classification, IT risk assessment and Mitigation strategies for IT applications.
  • Provide guidance and share knowledge and participate in performing procedures focusing on complex, or specialized issues in a regulatory environment. Work with the client to create plans for accomplishing engagement objectives and a strategy that complies with professional standards and addresses the risks inherent in the engagement
  • Assist Senior Managers in driving the business development process on existing client engagements by associating with clients and executing the deliverables in the most efficient manner.
  • Identify opportunities in existing accounts to cross-sell other EY services.
  • Planning and monitoring of the project deliverables from the team.
  • Create innovative insights for clients, adapts methods & practices to fit operational team needs & contributes to thought leadership documents.
  • Demonstrate team work by working with cross functional teams across service lines in completing the deliverables within the timelines
  • Maintain a strong client focus by effectively serving client needs and developing productive working relationships with client personnel. Stay abreast of current business and economic developments and new pronouncements/standards relevant to the client's business.
  • Regular status reporting to the Senior Managers, Partners, Directors and onsite coordinators.
  • Actively contribute to improving operational efficiency on projects & internal initiatives.
  • Demonstrate a detailed knowledge of market trends, competitor activities, EY products and service lines.
  • Demonstrate flexibility to travel to the customer locations on need basis
  • Conduct performance reviews and contribute to performance feedback for staff and senior staff
  • Foster teamwork, quality culture and lead by example
  • Understand and follow workplace policies and procedures
  • Training and mentoring of project resources
  • Participate in the organization-wide initiatives
  • Lead practice initiatives and portfolios
  • Market trend +Digital trends.
  • Cross skill and cross train the team members as per the business requirements
  • Skills and attributes for success

  • Quality & Compliance managed services and Consulting experience in of Life Sciences Domain.
  • Sound domain knowledge in Pharmaceutical industry in the areas of Quality and Compliance
  • Strong knowledge of Computerized Systems validation concepts such as GAMP 5 - A Risk-Based Approach to Compliant GxP Computerized Systems
  • Has worked in executing the Validation Deliverables in software implementation projects
  • Strong knowledge of standards such as USFDA 21 CFR Part 11, EU GMP Annex 11,
  • Strong knowledge of regulations such as USFDA, WHO, HIPAA, TGA, MCC, Anvisa etc.
  • Versed with ICH guidelines, ISPE framework on Risk management, System Development Life Cycle concepts.
  • Strong Knowledge on Enterprise IT applications like LIMS, SAP, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc. in Pharmaceutical organization.
  • Versed with SOP documentation, analysing the work instructions, user manuals
  • Strong knowledge of Quality System Elements such as, Deviation, CAPA, and Change Controls etc. as they relate to Computer Systems
  • Strong understanding of Data Integrity requirements
  • Governance and reporting

    Knowledge of Incident Management, Change Management, Periodic Review, Vendor Management, Quality Management Review procedures.

    Strong Knowledge on authoring and review of Validation Deliverables such as Validation Plan & report, Requirement specifications, Risk Analysis, Qualification Protocols & reports, Test Scripts, Traceability Matrix etc.

    Has supported Audits / Inspections

    To qualify for the role, you must have

  • (Electronics, Electronics & Telecommunications, Comp. Science)/Postgraduate in Science (Preferably in Chemistry/Biochemistry) with 10-12 years of experience with Big 4 or Multi-National Regulatory Compliance companies
  • Good interpersonal skills; Good written and presentational skills
  • At managerial positions within Information Technology (IT) and/or Quality Assurance (QA) for major organizations
  • Experience in managing team and solution designing
  • Ideally, you’ll also have

  • Certified Software Quality Engineer (CSQE), Certified Software Quality Assurance (CSQA)
  • ISO 9001:2015 Lead Auditor, Quality Auditor Certification (CQA)
  • Information Security or Risk Management certifications
  • Project Management
  • What we look for

    A Team of people with commercial acumen, technical experience and enthusiasm to learn new things in this fast-moving environment with consulting skills.

    An opportunity to be a part of market-leading, multi-disciplinary team of 1400 + professionals, in the only integrated global transaction business worldwide.

    Opportunities to work with EY Consulting practices globally with leading businesses across a range of industries

    What working at EY offers

    At EY, we’re dedicated to helping our clients, from start–ups to Fortune 500 companies — and the work we do with them is as varied as they are.

    You get to work with inspiring and meaningful projects. Our focus is education and coaching alongside practical experience to ensure your personal development. We value our employees and you will be able to control your own development with an individual progression plan. You will quickly grow into a responsible role with challenging and stimulating assignments. Moreover, you will be part of an interdisciplinary environment that emphasizes high quality and knowledge exchange. Plus, we offer:

  • Support, coaching and feedback from some of the most engaging colleagues around
  • Opportunities to develop new skills and progress your career
  • The freedom and flexibility to handle your role in a way that’s right for you
  • EY | Building a better working world 

    This advertiser has chosen not to accept applicants from your region.

    RC - REGULATORY COMPLIANCE - REGULATORY COMPLIANCE - Senior

    Chennai, Tamil Nadu EY

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    The opportunity

    We’re looking for Senior with expertise in Computer System Validation and stakeholder management to join our EY-Regulatory Compliance team. This is a fantastic opportunity to be part of a leading firm whilst being instrumental in the growth of emerging service offering.

    Your key responsibilities

  • Actively contribute to the IT applications project management initiatives that includes Validation activities as per GAMP Life Cycle approach
  • Integrate technology with business process transformation programs like SAP, LIMS, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc.
  • Troubleshoot IT application related issues and suggest recommendations for solutions in consultation with relevant functions.
  • Perform Gap assessment and Remediation procedures for legacy applications to ensure validation policies is in line with Life Cycle Approach
  • Perform Software classification, IT risk assessment and Mitigation strategies for IT applications.
  • Provide guidance and share knowledge and participate in performing procedures focusing on complex, or specialized issues in a regulatory environment. Work with the client to create plans for accomplishing engagement objectives and a strategy that complies with professional standards and addresses the risks inherent in the engagement
  • Assist Senior Managers in driving the business development process on existing client engagements by associating with clients and executing the deliverables in the most efficient manner.
  • Create innovative insights for clients, adapts methods & practices to fit operational team needs & contributes to thought leadership documents.
  • Demonstrate team work by working with cross functional teams across service lines in completing the deliverables within the timelines
  • Maintain a strong client focus by effectively serving client needs and developing productive working relationships with client personnel. Stay abreast of current business and economic developments and new pronouncements/standards relevant to the client's business.
  • Review status updates and prepare management presentations.
  • Actively contribute to improving operational efficiency on projects & internal initiatives.
  • Demonstrate a detailed knowledge of market trends, competitor activities, EY products and service lines.
  • Contribute to performance feedback for staff
  • Foster teamwork and a positive learning culture
  • Understand and follow workplace policies and procedures
  • Training and mentoring of project resources
  • Cross skill and cross train the team members as per the business requirements
  • Skills and attributes for success

  • Prior experience of leading quality and compliance projects in Regulatory Compliance.
  • Sound domain knowledge in Pharmaceutical industry in the areas of Quality control, Quality assurance
  • Strong knowledge of Computerized Systems validation concepts such as GAMP 5 - A Risk-Based Approach to Compliant GxP Computerized Systems
  • Hands on experience of preparing validation deliverables for software implementation projects
  • Sound understanding of standards such as USFDA 21 CFR Part 11, EU GMP Annex 11
  • Good understanding of regulations such as USFDA, WHO, HIPAA, TGA, MCC, Anvisa etc.
  • Well versed with ICH guidelines, ISPE framework on Risk management, and SDLC
  • Strong Knowledge on Enterprise IT applications like LIMS, SAP, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc. in Pharmaceutical organization
  • Proficient in SOP documentation, drafting work instructions/user manuals, authoring and review of Validation Deliverables such as Validation Plan & report, Requirement specifications, Risk Analysis, Qualification Protocols & reports, Test Scripts, Traceability Matrix etc.
  • Demonstrated track record in project management, governance, and reporting
  • Good understanding of Quality System Elements such as, Deviation, CAPA, and Change Controls etc.
  • Exposure to Data Integrity requirements and other applicable regulations
  • Knowledge of Incident Management, Change Management, Periodic Review, Vendor Management, Quality Management Review procedures
  • Prior experience of supporting Audits / Inspections
  • To qualify for the role, you must have

  • (Electronics, Electronics & Telecommunications, Comp. Science)/Postgraduate in Science (Preferably in Chemistry/Biochemistry) with 5-8 years of experience with Big 4 or Multi-National Regulatory Compliance companies
  • Good interpersonal skills; Good written and presentational skills
  • Ideally, you’ll also have

  • Certified Software Quality Engineer (CSQE), Certified Software Quality Assurance (CSQA)
  • ISO 9001:2015 Lead Auditor, Quality Auditor Certification (CQA)
  • Information Security or Risk Management certifications
  • What we look for

  • A Team of people with commercial acumen, technical experience and enthusiasm to learn new things in this fast-moving environment with consulting skills.
  • An opportunity to be a part of market-leading, multi-disciplinary team of 1400 + professionals, in the only integrated global transaction business worldwide.
  • Opportunities to work with EY Consulting practices globally with leading businesses across a range of industries
  • What working at EY offers

    At EY, we’re dedicated to helping our clients, from start–ups to Fortune 500 companies — and the work we do with them is as varied as they are.

    You get to work with inspiring and meaningful projects. Our focus is education and coaching alongside practical experience to ensure your personal development. We value our employees and you will be able to control your own development with an individual progression plan. You will quickly grow into a responsible role with challenging and stimulating assignments. Moreover, you will be part of an interdisciplinary environment that emphasizes high quality and knowledge exchange. Plus, we offer:

  • Support, coaching and feedback from some of the most engaging colleagues around
  • Opportunities to develop new skills and progress your career
  • The freedom and flexibility to handle your role in a way that’s right for yo
  • EY | Building a better working world 

    This advertiser has chosen not to accept applicants from your region.

    RC-REGULATORY COMPLIANCE-REGULATORY COMPLIANCE-Senior

    Bengaluru, Karnataka EY

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    The opportunity

    We’re looking for Senior with expertise in Computer System Validation and stakeholder management to join our EY-Regulatory Compliance team. This is a fantastic opportunity to be part of a leading firm whilst being instrumental in the growth of emerging service offering.

    Your key responsibilities

  • Actively contribute to the IT applications project management initiatives that includes Validation activities as per GAMP Life Cycle approach
  • Integrate technology with business process transformation programs like SAP, LIMS, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc.
  • Troubleshoot IT application related issues and suggest recommendations for solutions in consultation with relevant functions.
  • Perform Gap assessment and Remediation procedures for legacy applications to ensure validation policies is in line with Life Cycle Approach
  • Perform Software classification, IT risk assessment and Mitigation strategies for IT applications.
  • Provide guidance and share knowledge and participate in performing procedures focusing on complex, or specialized issues in a regulatory environment. Work with the client to create plans for accomplishing engagement objectives and a strategy that complies with professional standards and addresses the risks inherent in the engagement
  • Assist Senior Managers in driving the business development process on existing client engagements by associating with clients and executing the deliverables in the most efficient manner.
  • Create innovative insights for clients, adapts methods & practices to fit operational team needs & contributes to thought leadership documents.
  • Demonstrate team work by working with cross functional teams across service lines in completing the deliverables within the timelines
  • Maintain a strong client focus by effectively serving client needs and developing productive working relationships with client personnel. Stay abreast of current business and economic developments and new pronouncements/standards relevant to the client's business.
  • Review status updates and prepare management presentations.
  • Actively contribute to improving operational efficiency on projects & internal initiatives.
  • Demonstrate a detailed knowledge of market trends, competitor activities, EY products and service lines.
  • Contribute to performance feedback for staff
  • Foster teamwork and a positive learning culture
  • Understand and follow workplace policies and procedures
  • Training and mentoring of project resources
  • Cross skill and cross train the team members as per the business requirements
  • Skills and attributes for success

  • Prior experience of leading quality and compliance projects in Regulatory Compliance.
  • Sound domain knowledge in Pharmaceutical industry in the areas of Quality control, Quality assurance
  • Strong knowledge of Computerized Systems validation concepts such as GAMP 5 - A Risk-Based Approach to Compliant GxP Computerized Systems
  • Hands on experience of preparing validation deliverables for software implementation projects
  • Sound understanding of standards such as USFDA 21 CFR Part 11, EU GMP Annex 11,
  • Good understanding of regulations such as USFDA, WHO, HIPAA, TGA, MCC, Anvisa etc.
  • Well versed with ICH guidelines, ISPE framework on Risk management, and SDLC
  • Strong Knowledge on Enterprise IT applications like LIMS, SAP, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc. in Pharmaceutical organization
  • Proficient in SOP documentation, drafting work instructions/user manuals, authoring and review of Validation Deliverables such as Validation Plan & report, Requirement specifications, Risk Analysis, Qualification Protocols & reports, Test Scripts, Traceability Matrix etc.
  • Demonstrated track record in project management, governance, and reporting
  • Good understanding of Quality System Elements such as, Deviation, CAPA, and Change Controls etc.
  • Exposure to Data Integrity requirements and other applicable regulations
  • Knowledge of Incident Management, Change Management, Periodic Review, Vendor Management, Quality Management Review procedures
  • Prior experience of supporting Audits / Inspections
  • To qualify for the role, you must have

  • (Electronics, Electronics & Telecommunications, Comp. Science)/Postgraduate in Science (Preferably in Chemistry/Biochemistry) with 5-8 years of experience with Big 4 or Multi-National Regulatory Compliance companies
  • Good interpersonal skills; Good written and presentational skills
  • Ideally, you’ll also have

  • Certified Software Quality Engineer (CSQE), Certified Software Quality Assurance (CSQA)
  • ISO 9001:2015 Lead Auditor, Quality Auditor Certification (CQA)
  • Information Security or Risk Management certifications
  • What we look for

  • A Team of people with commercial acumen, technical experience and enthusiasm to learn new things in this fast-moving environment with consulting skills.
  • An opportunity to be a part of market-leading, multi-disciplinary team of 1400 + professionals, in the only integrated global transaction business worldwide.
  • Opportunities to work with EY Consulting practices globally with leading businesses across a range of industries
  • What working at EY offers

    At EY, we’re dedicated to helping our clients, from start–ups to Fortune 500 companies — and the work we do with them is as varied as they are.

    You get to work with inspiring and meaningful projects. Our focus is education and coaching alongside practical experience to ensure your personal development. We value our employees and you will be able to control your own development with an individual progression plan. You will quickly grow into a responsible role with challenging and stimulating assignments. Moreover, you will be part of an interdisciplinary environment that emphasizes high quality and knowledge exchange. Plus, we offer:

  • Support, coaching and feedback from some of the most engaging colleagues around
  • Opportunities to develop new skills and progress your career
  • The freedom and flexibility to handle your role in a way that’s right for you
  • EY | Building a better working world 

    This advertiser has chosen not to accept applicants from your region.

    RC-REGULATORY COMPLIANCE-REGULATORY COMPLIANCE-Manager

    Chennai, Tamil Nadu EY

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    The opportunity

    We’re looking for Manager with expertise in Computer System Validation and Stakeholder Management to join the leadership group of our EY-Regulatory Compliance team. This is a fantastic opportunity to be part of a leading firm whilst being instrumental in the growth of emerging service offering.

    Your key responsibilities

  • Actively contribute to the IT applications project management initiatives that includes Validation activities as per GAMP Life Cycle approach
  • Integrate technology with business process transformation programs like SAP, LIMS, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc.
  • Perform Gap assessment and Remediation procedures for legacy applications to ensure validation policies is in line with Life Cycle Approach
  • Perform Software classification, IT risk assessment and Mitigation strategies for IT applications.
  • Provide guidance and share knowledge and participate in performing procedures focusing on complex, or specialized issues in a regulatory environment. Work with the client to create plans for accomplishing engagement objectives and a strategy that complies with professional standards and addresses the risks inherent in the engagement
  • Assist Senior Managers in driving the business development process on existing client engagements by associating with clients and executing the deliverables in the most efficient manner.
  • Identify opportunities in existing accounts to cross-sell other EY services.
  • Planning and monitoring of the project deliverables from the team.
  • Create innovative insights for clients, adapts methods & practices to fit operational team needs & contributes to thought leadership documents.
  • Demonstrate team work by working with cross functional teams across service lines in completing the deliverables within the timelines
  • Maintain a strong client focus by effectively serving client needs and developing productive working relationships with client personnel. Stay abreast of current business and economic developments and new pronouncements/standards relevant to the client's business.
  • Regular status reporting to the Senior Managers, Partners, Directors and onsite coordinators.
  • Actively contribute to improving operational efficiency on projects & internal initiatives.
  • Demonstrate a detailed knowledge of market trends, competitor activities, EY products and service lines.
  • Demonstrate flexibility to travel to the customer locations on need basis
  • Conduct performance reviews and contribute to performance feedback for staff and senior staff
  • Foster teamwork, quality culture and lead by example
  • Understand and follow workplace policies and procedures
  • Training and mentoring of project resources
  • Participate in the organization-wide initiatives
  • Lead practice initiatives and portfolios
  • Market trend +Digital trends.
  • Cross skill and cross train the team members as per the business requirements
  • Skills and attributes for success

  • Quality & Compliance managed services and Consulting experience in of Life Sciences Domain.
  • Sound domain knowledge in Pharmaceutical industry in the areas of Quality and Compliance
  • Strong knowledge of Computerized Systems validation concepts such as GAMP 5 - A Risk-Based Approach to Compliant GxP Computerized Systems
  • Has worked in executing the Validation Deliverables in software implementation projects
  • Strong knowledge of standards such as USFDA 21 CFR Part 11, EU GMP Annex 11,
  • Strong knowledge of regulations such as USFDA, WHO, HIPAA, TGA, MCC, Anvisa etc.
  • Versed with ICH guidelines, ISPE framework on Risk management, System Development Life Cycle concepts.
  • Strong Knowledge on Enterprise IT applications like LIMS, SAP, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc. in Pharmaceutical organization.
  • Versed with SOP documentation, analysing the work instructions, user manuals
  • Strong knowledge of Quality System Elements such as, Deviation, CAPA, and Change Controls etc. as they relate to Computer Systems
  • Strong understanding of Data Integrity requirements
  • Governance and reporting
  • Knowledge of Incident Management, Change Management, Periodic Review, Vendor Management, Quality Management Review procedures.
  • Strong Knowledge on authoring and review of Validation Deliverables such as Validation Plan & report, Requirement specifications, Risk Analysis, Qualification Protocols & reports, Test Scripts, Traceability Matrix etc.
  • Has supported Audits / Inspections
  • T o qualify for the role, you must have

  • (Electronics, Electronics & Telecommunications, Comp. Science)/Postgraduate in Science (Preferably in Chemistry/Biochemistry) with 10-12 years of experience with Big 4 or Multi-National Regulatory Compliance companies
  • Good interpersonal skills; Good written and presentational skills
  • At managerial positions within Information Technology (IT) and/or Quality Assurance (QA) for major organizations
  • Experience in managing team and solution designing
  • Ideally, you’ll also have

  • Certified Software Quality Engineer (CSQE), Certified Software Quality Assurance (CSQA)
  • ISO 9001:2015 Lead Auditor, Quality Auditor Certification (CQA)
  • Information Security or Risk Management certifications
  • Project Management
  • What we look for

  • A Team of people with commercial acumen, technical experience and enthusiasm to learn new things in this fast-moving environment with consulting skills.
  • An opportunity to be a part of market-leading, multi-disciplinary team of 1400 + professionals, in the only integrated global transaction business worldwide.
  • Opportunities to work with EY Consulting practices globally with leading businesses across a range of industries
  • What working at EY offers

    At EY, we’re dedicated to helping our clients, from start–ups to Fortune 500 companies — and the work we do with them is as varied as they are.

    You get to work with inspiring and meaningful projects. Our focus is education and coaching alongside practical experience to ensure your personal development. We value our employees and you will be able to control your own development with an individual progression plan. You will quickly grow into a responsible role with challenging and stimulating assignments. Moreover, you will be part of an interdisciplinary environment that emphasizes high quality and knowledge exchange. Plus, we offer:

  • Support, coaching and feedback from some of the most engaging colleagues around
  • Opportunities to develop new skills and progress your career
  • The freedom and flexibility to handle your role in a way that’s right for you
  • EY | Building a better working world 

    This advertiser has chosen not to accept applicants from your region.

    RC - REGULATORY COMPLIANCE - REGULATORY COMPLIANCE - Senior

    Hyderabad, Andhra Pradesh EY

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    The opportunity

    We’re looking for Senior with expertise in Computer System Validation and stakeholder management to join our EY-Regulatory Compliance team. This is a fantastic opportunity to be part of a leading firm whilst being instrumental in the growth of emerging service offering.

    Your key responsibilities

  • Actively contribute to the IT applications project management initiatives that includes Validation activities as per GAMP Life Cycle approach
  • Integrate technology with business process transformation programs like SAP, LIMS, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc.
  • Troubleshoot IT application related issues and suggest recommendations for solutions in consultation with relevant functions.
  • Perform Gap assessment and Remediation procedures for legacy applications to ensure validation policies is in line with Life Cycle Approach
  • Perform Software classification, IT risk assessment and Mitigation strategies for IT applications.
  • Provide guidance and share knowledge and participate in performing procedures focusing on complex, or specialized issues in a regulatory environment. Work with the client to create plans for accomplishing engagement objectives and a strategy that complies with professional standards and addresses the risks inherent in the engagement
  • Assist Senior Managers in driving the business development process on existing client engagements by associating with clients and executing the deliverables in the most efficient manner.
  • Create innovative insights for clients, adapts methods & practices to fit operational team needs & contributes to thought leadership documents.
  • Demonstrate team work by working with cross functional teams across service lines in completing the deliverables within the timelines
  • Maintain a strong client focus by effectively serving client needs and developing productive working relationships with client personnel. Stay abreast of current business and economic developments and new pronouncements/standards relevant to the client's business.
  • Review status updates and prepare management presentations.
  • Actively contribute to improving operational efficiency on projects & internal initiatives.
  • Demonstrate a detailed knowledge of market trends, competitor activities, EY products and service lines.
  • Contribute to performance feedback for staff
  • Foster teamwork and a positive learning culture
  • Understand and follow workplace policies and procedures
  • Training and mentoring of project resources
  • Cross skill and cross train the team members as per the business requirements
  • Skills and attributes for success

  • Prior experience of leading quality and compliance projects in Regulatory Compliance.
  • Sound domain knowledge in Pharmaceutical industry in the areas of Quality control, Quality assurance
  • Strong knowledge of Computerized Systems validation concepts such as GAMP 5 - A Risk-Based Approach to Compliant GxP Computerized Systems
  • Hands on experience of preparing validation deliverables for software implementation projects
  • Sound understanding of standards such as USFDA 21 CFR Part 11, EU GMP Annex 11,
  • Good understanding of regulations such as USFDA, WHO, HIPAA, TGA, MCC, Anvisa etc.
  • Well versed with ICH guidelines, ISPE framework on Risk management, and SDLC
  • Strong Knowledge on Enterprise IT applications like LIMS, SAP, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc. in Pharmaceutical organization
  • Proficient in SOP documentation, drafting work instructions/user manuals, authoring and review of Validation Deliverables such as Validation Plan & report, Requirement specifications, Risk Analysis, Qualification Protocols & reports, Test Scripts, Traceability Matrix etc.
  • Demonstrated track record in project management, governance, and reporting
  • Good understanding of Quality System Elements such as, Deviation, CAPA, and Change Controls etc.
  • Exposure to Data Integrity requirements and other applicable regulations
  • Knowledge of Incident Management, Change Management, Periodic Review, Vendor Management, Quality Management Review procedures
  • Prior experience of supporting Audits / Inspections
  • To qualify for the role, you must have

  • (Electronics, Electronics & Telecommunications, Comp. Science)/Postgraduate in Science (Preferably in Chemistry/Biochemistry) with 5-8 years of experience with Big 4 or Multi-National Regulatory Compliance companies
  • Good interpersonal skills; Good written and presentational skills
  • Ideally, you’ll also have

  • Certified Software Quality Engineer (CSQE), Certified Software Quality Assurance (CSQA)
  • ISO 9001:2015 Lead Auditor, Quality Auditor Certification (CQA)
  • Information Security or Risk Management certifications
  • What we look for

  • A Team of people with commercial acumen, technical experience and enthusiasm to learn new things in this fast-moving environment with consulting skills.
  • An opportunity to be a part of market-leading, multi-disciplinary team of 1400 + professionals, in the only integrated global transaction business worldwide.
  • Opportunities to work with EY Consulting practices globally with leading businesses across a range of industries
  • What working at EY offers

    At EY, we’re dedicated to helping our clients, from start–ups to Fortune 500 companies — and the work we do with them is as varied as they are.

    You get to work with inspiring and meaningful projects. Our focus is education and coaching alongside practical experience to ensure your personal development. We value our employees and you will be able to control your own development with an individual progression plan. You will quickly grow into a responsible role with challenging and stimulating assignments. Moreover, you will be part of an interdisciplinary environment that emphasizes high quality and knowledge exchange. Plus, we offer:

  • Support, coaching and feedback from some of the most engaging colleagues around
  • Opportunities to develop new skills and progress your career
  • The freedom and flexibility to handle your role in a way that’s right for you
  • EY | Building a better working world 

    This advertiser has chosen not to accept applicants from your region.
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    About the latest Regulatory compliance Jobs in India !

    RC - REGULATORY COMPLIANCE - REGULATORY COMPLIANCE - Senior

    Noida, Uttar Pradesh EY

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    The opportunity

    We’re looking for Senior with expertise in Computer System Validation and stakeholder management to join our EY-Regulatory Compliance team. This is a fantastic opportunity to be part of a leading firm whilst being instrumental in the growth of emerging service offering.

    Your key responsibilities

  • Actively contribute to the IT applications project management initiatives that includes Validation activities as per GAMP Life Cycle approach
  • Integrate technology with business process transformation programs like SAP, LIMS, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc.
  • Troubleshoot IT application related issues and suggest recommendations for solutions in consultation with relevant functions.
  • Perform Gap assessment and Remediation procedures for legacy applications to ensure validation policies is in line with Life Cycle Approach
  • Perform Software classification, IT risk assessment and Mitigation strategies for IT applications.
  • Provide guidance and share knowledge and participate in performing procedures focusing on complex, or specialized issues in a regulatory environment. Work with the client to create plans for accomplishing engagement objectives and a strategy that complies with professional standards and addresses the risks inherent in the engagement
  • Assist Senior Managers in driving the business development process on existing client engagements by associating with clients and executing the deliverables in the most efficient manner.
  • Create innovative insights for clients, adapts methods & practices to fit operational team needs & contributes to thought leadership documents.
  • Demonstrate team work by working with cross functional teams across service lines in completing the deliverables within the timelines
  • Maintain a strong client focus by effectively serving client needs and developing productive working relationships with client personnel. Stay abreast of current business and economic developments and new pronouncements/standards relevant to the client's business.
  • Review status updates and prepare management presentations.
  • Actively contribute to improving operational efficiency on projects & internal initiatives.
  • Demonstrate a detailed knowledge of market trends, competitor activities, EY products and service lines.
  • Contribute to performance feedback for staff
  • Foster teamwork and a positive learning culture
  • Understand and follow workplace policies and procedures
  • Training and mentoring of project resources
  • Cross skill and cross train the team members as per the business requirements
  • Skills and attributes for success

  • Prior experience of leading quality and compliance projects in Regulatory Compliance.
  • Sound domain knowledge in Pharmaceutical industry in the areas of Quality control, Quality assurance
  • Strong knowledge of Computerized Systems validation concepts such as GAMP 5 - A Risk-Based Approach to Compliant GxP Computerized Systems
  • Hands on experience of preparing validation deliverables for software implementation projects
  • Sound understanding of standards such as USFDA 21 CFR Part 11, EU GMP Annex 11,
  • Good understanding of regulations such as USFDA, WHO, HIPAA, TGA, MCC, Anvisa etc.
  • Well versed with ICH guidelines, ISPE framework on Risk management, and SDLC
  • Strong Knowledge on Enterprise IT applications like LIMS, SAP, ELN, MES, Documentum, TrackWise, Veeva Vault, ValGenesis, Argus, Regulatory Information Management System etc. in Pharmaceutical organization
  • Proficient in SOP documentation, drafting work instructions/user manuals, authoring and review of Validation Deliverables such as Validation Plan & report, Requirement specifications, Risk Analysis, Qualification Protocols & reports, Test Scripts, Traceability Matrix etc.
  • Demonstrated track record in project management, governance, and reporting
  • Good understanding of Quality System Elements such as, Deviation, CAPA, and Change Controls etc.
  • Exposure to Data Integrity requirements and other applicable regulations
  • Knowledge of Incident Management, Change Management, Periodic Review, Vendor Management, Quality Management Review procedures
  • Prior experience of supporting Audits / Inspections
  • To qualify for the role, you must have

  • (Electronics, Electronics & Telecommunications, Comp. Science)/Postgraduate in Science (Preferably in Chemistry/Biochemistry) with 5-8 years of experience with Big 4 or Multi-National Regulatory Compliance companies
  • Good interpersonal skills; Good written and presentational skills
  • Ideally, you’ll also have

  • Certified Software Quality Engineer (CSQE), Certified Software Quality Assurance (CSQA)
  • ISO 9001:2015 Lead Auditor, Quality Auditor Certification (CQA)
  • Information Security or Risk Management certifications
  • What we look for

  • A Team of people with commercial acumen, technical experience and enthusiasm to learn new things in this fast-moving environment with consulting skills.
  • An opportunity to be a part of market-leading, multi-disciplinary team of 1400 + professionals, in the only integrated global transaction business worldwide.
  • Opportunities to work with EY Consulting practices globally with leading businesses across a range of industries
  • What working at EY offers

    At EY, we’re dedicated to helping our clients, from start–ups to Fortune 500 companies — and the work we do with them is as varied as they are.

    You get to work with inspiring and meaningful projects. Our focus is education and coaching alongside practical experience to ensure your personal development. We value our employees and you will be able to control your own development with an individual progression plan. You will quickly grow into a responsible role with challenging and stimulating assignments. Moreover, you will be part of an interdisciplinary environment that emphasizes high quality and knowledge exchange. Plus, we offer:

  • Support, coaching and feedback from some of the most engaging colleagues around
  • Opportunities to develop new skills and progress your career
  • The freedom and flexibility to handle your role in a way that’s right for you
  • EY | Building a better working world 

    This advertiser has chosen not to accept applicants from your region.

    Regulatory Compliance Manager

    Bengaluru, Karnataka TD SYNNEX

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    Job Summary

    Regulatory Compliance Manager will be responsible for managing the continued development and implementation of a global trade compliance program.

    Investigative skills will be applicable in managing trade compliance with other countries, as needed.

    Acting as a regional trade compliance representative, you will maintain an active role in assuring compliance of import/ export activities in the company owned subsidiaries and offices in APJ. In respect of Customs regulations and import/export licence controls.

    Apply continuity with the global trade compliance programs by country.

    You will be responsible for identifying, prioritizing and addressing trade compliance risk and Customs compliance risk.

    Job Description

    The initial focus of the Regulatory Compliance Manager is Export Control matters. This includes resolving potential DPL matches, transactional work with stakeholders, review of compliance holds on strategic or controlled goods-based end use/end user. The Regulatory Compliance Manager is responsible for collating and analyzing metrics related to export controls. The job will also involve supporting integration of systematic export controls into ERP systems. The role will develop and extend into areas of Customs (import/export) operational controls and will be responsible for process improvement and productivity improvements in that area.

    Responsibilities:
    • Be a subject matter expert and escalation person for matters related to trade compliance – export control, sanctions, Customs compliance.

    • Be a facilitator to design and implement improved trade compliance programs working with vendors, brokers, and related internal and external business partners.

    • Communicating and meeting with relevant Government authorities as needed.

    • Complete timely and compliant transaction controls and reviews.

    • Prepare and present relevant data analytics to support decision making

    • Backup other APJ Trade Compliance activities, if required.

    • The role will not line manage staff

    Knowledge, Skills and Experience:
    • 5 to 8 Years of relevant international trade, import and export experience.

    • University Degree or equivalent. Major in Legal, International Trade, Logistics or relevant preferred. Optional for candidates who has more relevant experience.

    • Experience on Technology sector.

    • Good technical and practical knowledge in customs and export control regulations in India, experience in Asia Pacific is a plus.

    • Knowledge of US Export Administration Regulation and APJ Import and Export regulations.

    • Operates without supervision within established guidelines.

    • High level of independent thinking and problem-solving capabilities

    • Able to identify and address potential risk at trade compliance

    • Good IT skills (Microsoft office applications etc.).

    • Able to provide interpretation of Regulations to internal and external business partners

    • Able to converse and write effectively in English. Able to speak/ read in second language with Asia Pacific is an advantage but not mandatory.

    • Possesses strong multi-cultural interpersonal skills.

    • Able to constructively work under stress and pressure when faced with high workloads and deadlines.

    • Able to maintain and promote social, ethical, and organizational standards in conducting internal and external business activities.

    • Able to maintain confidentiality of sensitive information.

    • Able to build solid, effective working relationships with others.

    • Able to exhibit ability to be sensitive to the needs, concerns, and feelings of others.

    • Able to quickly learn new systems and technology.

    Working Conditions:
    • Consistent non-standard work or overtime as business requires.

    • On-call availability required as necessary.

    • Professional, office environment.

    • Full-time working week with some work hours flexibility expected

    What’s In It For You?

    • Elective Benefits: Our programs are tailored to your country to best accommodate your lifestyle.
    • Grow Your Career: Accelerate your path to success (and keep up with the future) with formal programs on leadership and professional development, and many more on-demand courses.
    • Elevate Your Personal Well-Being: Boost your financial, physical, and mental well-being through seminars, events, and our global Life Empowerment Assistance Program.
    • Diversity, Equity & Inclusion: It’s not just a phrase to us; valuing every voice is how we succeed. Join us in celebrating our global diversity through inclusive education, meaningful peer-to-peer conversations, and equitable growth and development opportunities.
    • Make the Most of our Global Organization : Network with other new co-workers within your first 30 days through our onboarding program.
    • Connect with Your Community: Participate in internal, peer-led inclusive communities and activities, including business resource groups, local volunteering events, and more environmental and social initiatives.

    This advertiser has chosen not to accept applicants from your region.

    Regulatory Compliance Manager

    Mumbai, Maharashtra TD SYNNEX

    Posted today

    Job Viewed

    Tap Again To Close

    Job Description

    Job Summary

    Regulatory Compliance Manager will be responsible for managing the continued development and implementation of a global trade compliance program.

    Investigative skills will be applicable in managing trade compliance with other countries, as needed.

    Acting as a regional trade compliance representative, you will maintain an active role in assuring compliance of import/ export activities in the company owned subsidiaries and offices in APJ. In respect of Customs regulations and import/export licence controls.

    Apply continuity with the global trade compliance programs by country.

    You will be responsible for identifying, prioritizing and addressing trade compliance risk and Customs compliance risk.

    Job Description

    The initial focus of the Regulatory Compliance Manager is Export Control matters. This includes resolving potential DPL matches, transactional work with stakeholders, review of compliance holds on strategic or controlled goods-based end use/end user. The Regulatory Compliance Manager is responsible for collating and analyzing metrics related to export controls. The job will also involve supporting integration of systematic export controls into ERP systems. The role will develop and extend into areas of Customs (import/export) operational controls and will be responsible for process improvement and productivity improvements in that area.

    Responsibilities:
    • Be a subject matter expert and escalation person for matters related to trade compliance – export control, sanctions, Customs compliance.

    • Be a facilitator to design and implement improved trade compliance programs working with vendors, brokers, and related internal and external business partners.

    • Communicating and meeting with relevant Government authorities as needed.

    • Complete timely and compliant transaction controls and reviews.

    • Prepare and present relevant data analytics to support decision making

    • Backup other APJ Trade Compliance activities, if required.

    • The role will not line manage staff

    Knowledge, Skills and Experience:
    • 5 to 8 Years of relevant international trade, import and export experience.

    • University Degree or equivalent. Major in Legal, International Trade, Logistics or relevant preferred. Optional for candidates who has more relevant experience.

    • Experience on Technology sector.

    • Good technical and practical knowledge in customs and export control regulations in India, experience in Asia Pacific is a plus.

    • Knowledge of US Export Administration Regulation and APJ Import and Export regulations.

    • Operates without supervision within established guidelines.

    • High level of independent thinking and problem-solving capabilities

    • Able to identify and address potential risk at trade compliance

    • Good IT skills (Microsoft office applications etc.).

    • Able to provide interpretation of Regulations to internal and external business partners

    • Able to converse and write effectively in English. Able to speak/ read in second language with Asia Pacific is an advantage but not mandatory.

    • Possesses strong multi-cultural interpersonal skills.

    • Able to constructively work under stress and pressure when faced with high workloads and deadlines.

    • Able to maintain and promote social, ethical, and organizational standards in conducting internal and external business activities.

    • Able to maintain confidentiality of sensitive information.

    • Able to build solid, effective working relationships with others.

    • Able to exhibit ability to be sensitive to the needs, concerns, and feelings of others.

    • Able to quickly learn new systems and technology.

    Working Conditions:
    • Consistent non-standard work or overtime as business requires.

    • On-call availability required as necessary.

    • Professional, office environment.

    • Full-time working week with some work hours flexibility expected

    What’s In It For You?

    • Elective Benefits: Our programs are tailored to your country to best accommodate your lifestyle.
    • Grow Your Career: Accelerate your path to success (and keep up with the future) with formal programs on leadership and professional development, and many more on-demand courses.
    • Elevate Your Personal Well-Being: Boost your financial, physical, and mental well-being through seminars, events, and our global Life Empowerment Assistance Program.
    • Diversity, Equity & Inclusion: It’s not just a phrase to us; valuing every voice is how we succeed. Join us in celebrating our global diversity through inclusive education, meaningful peer-to-peer conversations, and equitable growth and development opportunities.
    • Make the Most of our Global Organization : Network with other new co-workers within your first 30 days through our onboarding program.
    • Connect with Your Community: Participate in internal, peer-led inclusive communities and activities, including business resource groups, local volunteering events, and more environmental and social initiatives.

    This advertiser has chosen not to accept applicants from your region.
     

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