Regulatory Affairs Senior Manager

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

Pharmalex, a Cencora company, is looking for a Senior Manager Regulatory Affairs to join the team, remotely based in Spain.

Key Responsibilities :

• Develop and maintain strong client relationships and help drive opportunities for increased service support to Line Manager.
• Participate in regulatory processes to gain and maintain marketing authorizations for human and veterinary medicinal products (applications, renewals, variations), including medical devices, cosmetics, food supplements, and herbal products.
• Prepare, review, and compile documents within the framework of regulatory affairs projects.
• Communicate with clients and Health Authorities.
• Support scientific advice procedures and represent clients with health authorities.
• Plan and execute client projects in accordance with KPIs. Coordinate project teams with colleagues and external partners.
• Provide general guidance (consultancy) to colleagues and clients regarding Regulatory Strategy and Procedure Management.
• Develop and maintain personal regulatory knowledge, apply it to client projects, and share actively with colleagues.
• Present seminars and lectures for colleagues, clients, and professional audiences. Contribute actively to department expertise.
• Support VDC strategy implementation and optimization.
• Optimize internal processes and ensure compliance.
• Provide operational support to colleagues daily.
• Contribute to commercial, marketing, and business development activities, including proposal input.
• Oversee project delivery within budget and resolve invoicing queries.
• Provide on-site regulatory support to GCS clients as agreed with the Head of VDC REG.
• Take on other tasks aligned with abilities upon agreement with your Line Manager / Practice Area Lead / Head of VDC REG.
• Lead and coach direct reports; conduct evaluations and personal development meetings.
• Monitor utilization, capacities, and capabilities of team members and escalate issues as needed.

Education & Experience :

University degree in Life Science.

Proven professional experience in the area of responsibility; extensive knowledge of the discipline or department, capable of solving complex problems, with a strong understanding of the business.

Minimum Skills, Knowledge & Ability requirements :

What Cencora offers

Benefits outside the US may vary by country and will be aligned to local practices. Eligibility and effective date may differ for some benefits and team members under collective bargaining agreements.

Full-time position.

Affiliated Companies

PharmaLex Spain S.L.U.

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