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(R), Compeed(R), Solpadeine(R), NiQuitin(R), 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 a Senior Regulatory Affairs Professional within Regulatory Operations, you will play a key role in coordinating and managing regulatory publishing activities across Perrigo’s portfolio, helping to ensure high:quality, compliant and timely delivery of submissions and related regulatory operational outputs.
You will be responsible for supporting and coordinating publishing planning, submission readiness, document workflows and operational delivery activities, working closely with Regulatory Affairs colleagues across Lifecycle Management, Category, Cluster and other cross:functional partners. You will help ensure that submission packages are prepared, quality checked and delivered in line with applicable regulatory requirements, internal standards and business priorities.
This role will also support the development and improvement of regulatory operations processes, systems and metrics. You will contribute to the optimisation of ways of working, support data and process quality, and help embed consistent, scalable approaches across Regulatory Affairs. You will work with stakeholders to identify operational risks, resolve delivery barriers and support timely execution of regulatory activities.
Acting as a senior professional within the Regulatory Operations team, you will provide technical expertise, coordination support and guidance to others. You will help drive operational discipline, right:first:time quality and continuous improvement across publishing, process, systems and performance management activities.
This role offers the opportunity to make a meaningful impact within the Regulatory Affairs organisation by supporting compliant regulatory delivery, improving operational ways of working and helping Perrigo build more digitally enabled, data:led and scalable regulatory operations capability.
Scope of the Role
:Leads and coordinates regulatory publishing and operational delivery activities across multiple products, markets and regulatory workstreams.
:Provides expertise in publishing coordination, submission readiness, document management, regulatory systems, process improvement and operational metrics. Acts as a senior Regulatory Operations professional, supporting governance, continuous improvement and consistent ways of working.
:Leads publishing activities supporting regulatory submissions, lifecycle management, commitments and business priorities. Operates with a high degree of autonomy, accountable for recommendations, issue resolution and technical guidance within delegated authority.
:Acts as a senior individual contributor and mentor, supporting delivery across publishing, systems, document management, process improvement and metrics. Collaborates closely with Lifecycle Management, Category and Cluster Regulatory Affairs, Quality, Supply Chain, Safety, IT and other stakeholders to ensure compliant, timely and efficient operations.
:Provides support across broader regulatory activities as business needs require.
Publishing Coordination and Operational Delivery
:Lead and coordinate publishing activities for regulatory submissions across medicinal products and globa
Salary: Competitive
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Category: Science
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