Professional Regulatory Affairs - Lifecycle Management - Non-Medicines
Perrigo Company plc
August 19, 2026
Remote friendly (Allegan, MI)
United States
Corporate Functions
Description Overview
Regulatory Affairs Professional within Non-Medicinal Lifecycle Management—support non-medicinal portfolio (cosmetics, VMS, general products, and other non-medicinal classifications such as medical devices) across the product lifecycle. Contribute to regulatory strategy and execution to deliver compliant, high-quality regulatory outcomes.
Responsibilities
- Manage lifecycle management activities: prepare/maintain/deliver regulatory documentation, product/technical files, notifications, registrations, and supporting records per global requirements.
- Identify regulatory risks, support mitigation, and ensure timely, compliant regulatory filings and documentation updates to maintain supply continuity, consumer safety, and market access.
- Independently manage complex post-market lifecycle changes and related filings/updates across products and markets; lead workstreams within LCM remit.
- Assess and manage complex post-market lifecycle changes with cross-functional teams/authorities; identify data requirements and update regulatory documentation/product files.
- Determine regulatory pathway/classification for complex changes with clear rationale and risk-based recommendations; maintain regulatory intelligence.
- Establish/maintain/update product information files, technical files, regulatory records and supporting documentation in compliance with applicable legislation.
- Manage central notifications, registration filings, renewals, documentation updates; prepare files, answer RFIs, manage timelines; develop/update master labels.
- Support audits/CAPA follow-up and mitigate risks to avoid supply disruption.
- Represent Regulatory in project teams; communicate requirements, risks, and proposals; support improvements to lifecycle processes.
- Ensure robust handover/transition of regulatory documentation and implementation requirements at launch and post-market.
Experience & Qualifications
- Typically 3–5 years in Regulatory Affairs; relevant scientific/technical degree preferred.
- Experience with lifecycle submissions, dossier maintenance, and cross-functional issue resolution.
Benefits
- Competitive compensation; benefits for you and your family; career development opportunities.
- Hybrid work: ability to work two days/week from home in many roles.
Application Instructions
- Apply via the APPLY button at the bottom of the application; submit all resumes/CVs in English.
Regulatory Affairs Professional within Non-Medicinal Lifecycle Management—support non-medicinal portfolio (cosmetics, VMS, general products, and other non-medicinal classifications such as medical devices) across the product lifecycle. Contribute to regulatory strategy and execution to deliver compliant, high-quality regulatory outcomes.
Responsibilities
- Manage lifecycle management activities: prepare/maintain/deliver regulatory documentation, product/technical files, notifications, registrations, and supporting records per global requirements.
- Identify regulatory risks, support mitigation, and ensure timely, compliant regulatory filings and documentation updates to maintain supply continuity, consumer safety, and market access.
- Independently manage complex post-market lifecycle changes and related filings/updates across products and markets; lead workstreams within LCM remit.
- Assess and manage complex post-market lifecycle changes with cross-functional teams/authorities; identify data requirements and update regulatory documentation/product files.
- Determine regulatory pathway/classification for complex changes with clear rationale and risk-based recommendations; maintain regulatory intelligence.
- Establish/maintain/update product information files, technical files, regulatory records and supporting documentation in compliance with applicable legislation.
- Manage central notifications, registration filings, renewals, documentation updates; prepare files, answer RFIs, manage timelines; develop/update master labels.
- Support audits/CAPA follow-up and mitigate risks to avoid supply disruption.
- Represent Regulatory in project teams; communicate requirements, risks, and proposals; support improvements to lifecycle processes.
- Ensure robust handover/transition of regulatory documentation and implementation requirements at launch and post-market.
Experience & Qualifications
- Typically 3–5 years in Regulatory Affairs; relevant scientific/technical degree preferred.
- Experience with lifecycle submissions, dossier maintenance, and cross-functional issue resolution.
Benefits
- Competitive compensation; benefits for you and your family; career development opportunities.
- Hybrid work: ability to work two days/week from home in many roles.
Application Instructions
- Apply via the APPLY button at the bottom of the application; submit all resumes/CVs in English.