Professional Regulatory Affairs - Lifecycle Management - Non-Medicines
Perrigo Company plc
August 19, 2026
Remote friendly (Morristown, NJ)
United States
Corporate Functions
Description Overview
You will support Perrigo’s non-medicinal portfolio (cosmetics, VMS, general products, and other non-medicinal classifications such as medical devices) across the product lifecycle, developing and executing regulatory strategies to deliver compliant regulatory outcomes.
Responsibilities
- Manage lifecycle management activities: prepare, maintain, and deliver regulatory documentation, product/technical files, notifications, registrations, and supporting records in line with global requirements and business priorities.
- Identify regulatory risks and support mitigation; ensure timely, compliant filings and documentation updates to maintain supply continuity, consumer safety, and market access.
- Independently manage complex post-market lifecycle changes end-to-end; seek alignment for high-risk decisions and provide risk-based recommendations within delegated authority.
- Lead workstreams/workstream delivery across multiple products or markets.
- Assess and manage complex post-market lifecycle changes; work with cross-functional teams/authorities to identify data requirements and update regulatory documentation/product files.
- Determine regulatory pathway/classification for complex changes; provide rationale and risk-based recommendations.
- Establish/maintain/review/approve/update product information files, technical files, regulatory records, and supporting documentation.
- Manage central notifications, registration filings/renewals, documentation updates; prepare files, answer RFIs, and manage timelines.
- Develop/approve updated master labels; support implementation readiness and approval traceability.
- Support audits and CAPA reporting/follow-up; mitigate risks to avoid supply disruption.
- Represent Regulatory in project teams; communicate requirements, risks, and proposals.
- Support RA authority communications; respond to lifecycle queries.
- Suggest and execute process improvements to improve quality/predictability of lifecycle delivery.
- Ensure robust handover/transition of product information files, technical documentation, regulatory decisions, and implementation requirements.
Experience Required / Qualifications
- Typically 3–5 years in Regulatory Affairs; relevant scientific/technical degree preferred.
- Experience across lifecycle submissions, dossier maintenance, and cross-functional issue resolution.
- Ability to represent Regulatory, lead workstreams with increasing independence, and manage complex regulatory matters.
Benefits
- Competitive compensation; benefits to support you and your family; career development opportunities.
- Hybrid working flexibility: ability to work two days a week from home in many roles.
Application Instructions
- Click the APPLY button at the bottom of the application. Submit all application materials (resumes/CVs) in English.
You will support Perrigo’s non-medicinal portfolio (cosmetics, VMS, general products, and other non-medicinal classifications such as medical devices) across the product lifecycle, developing and executing regulatory strategies to deliver compliant regulatory outcomes.
Responsibilities
- Manage lifecycle management activities: prepare, maintain, and deliver regulatory documentation, product/technical files, notifications, registrations, and supporting records in line with global requirements and business priorities.
- Identify regulatory risks and support mitigation; ensure timely, compliant filings and documentation updates to maintain supply continuity, consumer safety, and market access.
- Independently manage complex post-market lifecycle changes end-to-end; seek alignment for high-risk decisions and provide risk-based recommendations within delegated authority.
- Lead workstreams/workstream delivery across multiple products or markets.
- Assess and manage complex post-market lifecycle changes; work with cross-functional teams/authorities to identify data requirements and update regulatory documentation/product files.
- Determine regulatory pathway/classification for complex changes; provide rationale and risk-based recommendations.
- Establish/maintain/review/approve/update product information files, technical files, regulatory records, and supporting documentation.
- Manage central notifications, registration filings/renewals, documentation updates; prepare files, answer RFIs, and manage timelines.
- Develop/approve updated master labels; support implementation readiness and approval traceability.
- Support audits and CAPA reporting/follow-up; mitigate risks to avoid supply disruption.
- Represent Regulatory in project teams; communicate requirements, risks, and proposals.
- Support RA authority communications; respond to lifecycle queries.
- Suggest and execute process improvements to improve quality/predictability of lifecycle delivery.
- Ensure robust handover/transition of product information files, technical documentation, regulatory decisions, and implementation requirements.
Experience Required / Qualifications
- Typically 3–5 years in Regulatory Affairs; relevant scientific/technical degree preferred.
- Experience across lifecycle submissions, dossier maintenance, and cross-functional issue resolution.
- Ability to represent Regulatory, lead workstreams with increasing independence, and manage complex regulatory matters.
Benefits
- Competitive compensation; benefits to support you and your family; career development opportunities.
- Hybrid working flexibility: ability to work two days a week from home in many roles.
Application Instructions
- Click the APPLY button at the bottom of the application. Submit all application materials (resumes/CVs) in English.