Technical Architect (DPO)

HCLTech; Massachusetts; On-site; USD 90,000 - 130,000; Full time

Job summary

HCL Technologies Limited in Massachusetts is seeking a Technical Architect (DPO) to guide regulatory strategy for product development, oversee pre-marketing submissions, and ensure global compliance.

You will coordinate licenses, technical dossiers, labeling, and promotions, support audits, and partner with cross-functional teams on US and international regulatory issues. This role emphasizes efficient processes and timely regulatory approvals across markets.

Responsibilities

• Provide regulatory guidance to product development teams in defining regulatory strategies, pre-marketing, and related submissions to support optimal timelines for modified product launches in the global market.
• Execute on the submission of licenses and authorizations for the maintenance of existing products, international registrations, and dossiers, including, but not limited to Change Notifications, Technical Documents, and correspondence with Notified Bodies.
• Guide conformance with applicable regulations in product development, support of claims, content labeling, and promotional materials.
• Define data and information needed for regulatory approvals.
• Develop labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations.
• Provide Regulatory Affairs support during internal and external audits.
• Plan schedules for delivery of supporting documentations required for regulatory submissions on a project and monitors project through completion.
• Assist in the development of improved and efficient processes practices for Regulatory Affairs processes.
• Represent Regulatory Affairs on cross-functional project teams, guiding and supporting product development teams on both US and international issues, including Purchased for Resale products.
• Partner with other functions to define and generate data to assist with regulatory submissions.
• Review and provide regulatory authorization for various changes to product, procedures, etc.
• Respond to requests from foreign governments and/or distributors to prepare and submit documentation for marketing approvals in other countries, as well as provide routine regulatory information to associates and affiliates.

Job description

Career Opportunities: Technical Architect (DPO) (188069)

Requisition ID188069-Posted11/09/2026

• Provide regulatory guidance to product development teams in defining regulatory strategies, pre-marketing, and related submissions to support optimal timelines for modified product launches in the global market.
• Execute on the submission of licenses and authorizations for the maintenance of existing products, international registrations, and dossiers, including, but not limited to Change Notifications, Technical Documents, and correspondence with Notified Bodies.
• Guide conformance with applicable regulations in product development, support of claims, content labeling, and promotional materials.
• Define data and information needed for regulatory approvals.
• Develop labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations.
• Provide Regulatory Affairs support during internal and external audits.
• Plan schedules for delivery of supporting documentations required for regulatory submissions on a project and monitors project through completion.
• Assist in the development of improved and efficient processes practices for Regulatory Affairs processes.
• Represent Regulatory Affairs on cross-functional project teams, guiding and supporting product development teams on both US and international issues, including Purchased for Resale products.
• Partner with other functions to define and generate data to assist with regulatory submissions.
• Review and provide regulatory authorization for various changes to product, procedures, etc.
• Respond to requests from foreign governments and/or distributors to prepare and submit documentation for marketing approvals in other countries, as well as provide routine regulatory information to associates and affiliates.

Key Responsibilities

• Provide regulatory guidance to product development teams in defining regulatory strategies, pre-marketing, and related submissions to support optimal timelines for modified product launches in the global market.
• Execute on the submission of licenses and authorizations for the maintenance of existing products, international registrations, and dossiers, including, but not limited to Change Notifications, Technical Documents, and correspondence with Notified Bodies.
• Guide conformance with applicable regulations in product development, support of claims, content labeling, and promotional materials.
• Define data and information needed for regulatory approvals.
• Develop labeling specifications and approves proposed labeling, packaging, advertising and promotional materials after evaluating conformance to regulations.
• Provide Regulatory Affairs support during internal and external audits.
• Plan schedules for delivery of supporting documentations required for regulatory submissions on a project and monitors project through completion.
• Assist in the development of improved and efficient processes practices for Regulatory Affairs processes.
• Represent Regulatory Affairs on cross-functional project teams, guiding and supporting product development teams on both US and international issues, including Purchased for Resale products.
• Partner with other functions to define and generate data to assist with regulatory submissions.
• Review and provide regulatory authorization for various changes to product, procedures, etc.
• Respond to requests from foreign governments and/or distributors to prepare and submit documentation for marketing approvals in other countries, as well as provide routine regulatory information to associates and affiliates.