Regulatory Affairs Associate
il y a 1 semaine
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®, ACO®, 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 a blended-branded business to win in self-care. **Description Overview**: In tis role which focuses on biocides, you will work across several territories, giving you the chance to develop skills for executing and managing regulatory projects. You will be handling licensing and post marketing activities for Perrigo products. **Scope of the Role**: - Support in daily work for the Biocidal products portfolio: ensure compliance of our product with the relevant pieces of legislation including updating dossiers, approving artworks, label claims and associated supporting documentation. - Carry out other related regulatory affairs duties as required. - Provide administrative support to change control process, by driving assignment and follow-up processes, ensuring compliance with internal and, when applicable, external requirements and deadlines - Support the Regulatory Intelligence & Policy Manager by monitoring of specified sources across a very wide range of regulatory product qualifications to identify any intelligence relevant to the Perrigo business - Summarise and document intelligence, ensuring key information is captured for communication to the business - Other administrative support as required such as meeting preparations, information database updates - Accurately and timely updating of internal working schedules, related to assigned tasks. **Experience Required**: The ability to support several concurrent projects/products in a flexible manner both autonomously and in a team environment. Must have good Time-Management skills. Must be collaborative and able to influence change. Cross-culturally competent and customer service oriented. Great communication skills. University degree (Bachelor’s degree). Degree in life science preferred. Or Must haves: Fluency in English. Exposure to biocides/EU-BPR **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** - 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. Our full Equal Employment Opportunity and Affirmative Action Policy Statement is available on our main career site in English and Spanish and will be provided in other accessible forms for persons with disabilities. #DIV #weareperrigo_
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Manager Regulatory Affairs
il y a 1 jour
Châtillon, France Perrigo Temps plein**General description**: 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...
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Cmc Regulatory Affairs Project Manager
il y a 7 jours
Châtillon, France Perrigo Temps pleinAt 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...
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Global CMC Regulatory Lead — Hybrid Role
il y a 6 jours
Châtillon, France Perrigo Temps pleinA global healthcare leader in Châtillon is seeking an Associate Director to lead Chemistry, Manufacturing & Control (CMC) strategies. The ideal candidate will have over 15 years of experience and a proven track record of regulatory compliance and submissions. This role involves overseeing a high-performing regulatory team, engaging with global health...
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Quality Assurance Associate
il y a 1 semaine
Viry-Châtillon, Île-de-France Perrigo France Temps pleinSearch by KeywordSearch by LocationSearch by Postal Code Search by LocationSearch by Postal CodeDistance2 mi 5 mi 10 mi 30 mi 50 miSearch by Postal Code Search by LocationShow More OptionsLoading...Country/RegionAllLocationAllJob CategoryAllOnsite or RemoteAllSelect How Often (in Days) To Receive An AlertSelect how often (in days) to receive an alert:Apply...
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Quality Assurance Associate
il y a 1 jour
Châtillon, France Perrigo Temps plein**Description Overview**: In this fixed term contract role (CDD 6 months) as Quality Assurance Associate you will work within the quality department to support operational processes. **Scope of the Role**: - Ensure adherence to critical procedures and compliance to requirements for record retention. - Set up and maintain Quality Agreements with...
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Quality Assurance Associate, Qp
il y a 5 jours
Châtillon, France Perrigo Temps pleinLa Société Perrigo est dédiée à l'amélioration de la qualité de vie en proposant des produits d’automédication de qualité, abordables et fiables, qui ont la confiance des consommateurs partout où ils sont vendus. Aidez-nous à le faire. **Description générale**: **Périmètre du poste**: - Ensure adherence to critical procedures and...
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Quality Assurance Associate, Qp
il y a 5 jours
Châtillon, France Perrigo Temps pleinAt 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...
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Responsable Affaires Règlementaires Cmc
il y a 7 jours
Châtillon, France Perrigo Temps pleinChez Perrigo, nous sommes guidés par notre mission d'améliorer la vie grâce à des solutions de santé et de bien-être de confiance, accessibles à tous. Nous sommes fiers d'être l'un des 10 leaders du marché européen de l'automédication et le plus grand fournisseur de marques distributeurs de médicaments en vente libre et de nutrition infantile aux...