Professional Regulatory Affairs - Regulatory Operations (Warsaw, PL, 02-653)
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At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All . We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone , we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.
Join us on our One Perrigo journey as we evolve to win in self-care.
Description Overview
We are excited to recruit an Associate Professional Regulatory Affairs within Regulatory Operations, you will play an important role in supporting Perrigo's regulatory systems, data and digital capabilities, helping to ensure regulatory information is accurate, compliant, accessible and effectively managed throughout the product lifecycle.
You will be responsible for maintaining and improving regulatory data, supporting system usage, identification of future requirements, develop processes and workflows, and contributing to the effective operation of regulatory platforms and tools. Working closely with Regulatory Affairs colleagues across the Operations team as well as with the Regulatory Affairs Lifecycle Management, Category, Cluster and other cross-functional teams, you will help ensure regulatory information data obligations are met and maintained to a high standard and supports compliant regulatory submissions, reporting and business activities.
This role will support the ongoing development and optimisation of regulatory operations systems, data governance processes and performance reporting. You will contribute to improving data quality, process consistency and system adoption, while helping identify opportunities to enhance efficiency, visibility and operational effectiveness across Regulatory Affairs.
Working collaboratively with stakeholders, you will support data investigations, process improvements, system enhancements and reporting activities. You will help identify and resolve data quality issues, support implementation of new ways of working and contribute to the successful delivery of regulatory operations initiatives.
As an experienced regulatory operations professional, you will apply your technical expertise and analytical skills to support effective system and data management practices. You will contribute to the continuous improvement of regulatory processes, systems and metrics, helping to promote operational excellence, right-first-time quality and a data-driven approach to decision making.
This role offers the opportunity to make a meaningful contribution within the Regulatory Affairs organisation by supporting regulatory systems and data capabilities that enable compliant regulatory delivery, improve operational efficiency and help Perrigo continue its digital transformation journey.
Scope of the Role
Manages regulatory systems and data activities across multiple products, markets and regulatory workstreams, supporting the accurate, compliant and efficient execution of regulatory operations.
Provides expertise in regulatory data management, systems, reporting and process improvement, helping to optimise business processes and enhance operational performance.
Contributes to governance, continuous improvement and operational excellence initiatives, driving data quality, process consistency and adoption of scalable ways of working across Regulatory Affairs.
Independently manages regulatory systems and data activities across products, markets and workstreams to support compliant, efficient regulatory operations.
Works independently within delegated authority, resolving operational issues and improving systems, data quality, workflows and processes.
Leads or contributes to systems, data governance, process improvement and digitalisation initiatives across products, functions and regulatory processes.
Partners across Regulatory Affairs, Quality, Supply Chain, Safety, IT and other stakeholders to support accurate data, effective system use and scalable ways of working.
May support other regulatory operations activities as business needs require.
Systems, Data & Digital Capability
Manage regulatory systems and data across products, markets and workstreams, ensuring information is accurate, complete, compliant and maintained to requirements.
Support administration, maintenance and optimisation of regulatory systems, workflows and data structures to improve usability, efficiency and data quality.
Investigate and resolve regulatory data issues, including discrepancies, process gaps and system-related challenges.
Support system enhancements, implementations, upgrades and change initiatives through requirements gathering, testing and business adoption.
Contribute to data governance, ensuring regulatory information is managed, traceable and aligned across systems, products and processes.
Process Improvement, Reporting & Operational Excellence
Develop, maintain and analyse regulatory metrics, reports and dashboards covering performance, workload, compliance, data quality and outcomes.
Use system and operational data to identify trends, risks and improvement opportunities, and provide recommendations.
Support SOPs, work instructions, business processes and data standards to drive consistency and scalability.
Contribute to digitalisation and process improvements that enhance efficiency, reporting, system adoption and user experience.
Represent regulatory systems and data requirements in cross-functional projects and business solutions.
Governance, Compliance & Stakeholder Partnership
Support inspection-ready regulatory systems and data in line with regulatory requirements, procedures and governance standards.
Partner with Regulatory Affairs, Quality, Supply Chain, Safety and IT to support system use, process compliance and operational delivery.
Assess and escalate data, system or process risks, supporting timely resolution and corrective actions.
Provide user guidance on regulatory systems, data processes and reporting requirements to promote consistent, compliant ways of working.
Maintain awareness of regulatory data standards, digital capabilities and industry trends to strengthen operations and data integrity.
Experience Required
Typically 3–5 years' experience in Regulatory Affairs for healthcare products, Regulatory Operations, regulatory systems, data management or related operational roles; relevant scientific, technical or regulatory degree preferred.
Experience working with regulatory systems, regulatory data, reporting, workflows or operational processes supporting regulatory activities.
Demonstrated ability to independently manage activities, resolve issues and coordinate effectively with cross-functional stakeholders.
Experience supporting process improvement, system enhancements, reporting or data quality initiatives.
Strong analytical, organisational and communication skills, with the ability to work effectively in a matrixed environment.
Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.
Find out more about Total Rewards at Perrigo.
Hybrid Working Approach
We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.
We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here
Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo
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Job details
How this role compares
Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.
We currently track 397 comparable Regulatory Affairs roles across 88 biopharma companies.
Salary context
122 of 397 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 397 comparable roles
+ 39 more countries
Seniority mix
318 of 397 peers have a known seniority level
Therapeutic area mix
33 of 397 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.