Regulatory Affairs Project Manager * Roche Mannheim

Your tasks:

• Leading and supporting regulatory strategies for global product submissions
• Ensuring compliance with international regulatory requirements and standards
• Collaborating with cross-functional teams, including R&D, Quality and Clinical to drive regulatory initiatives
• Providing regulatory guidance to support product development and lifecycle management
• Staying abreast of evolving regulatory trends and up‐ dates, and implementing best practices

Your qualification:

• Bachelor’s Degree in Life Sciences, Regulatory Affairs or a related field / alternatively completed vocational training with comparable experience in the regulatory field
• Profound work experience in Regulatory Affairs; preferred in Regulatory, R&D, Quality, and/or Clinical, with some experience in Healthcare regulatory affairs
• In-depth knowledge of global regulatory requirements, guidelines, and procedures especially for IVD instruments & medical device
• Strong organizational and communication skills
• Ability to multitask and effectively manage multiple projects simultaneously
• Self-motivated and capable of working independently in a self-management environment
• Fluent in English (for international meetings), German skills are not necessarily required
• Affinity for IT and good MS Office skills

* Franz & Wach is a signatory of the Diversity Charter. This job advertisement is basically addressed to people of any gender or age, any origin, orientation or identity!

Your contact to us

1.     Send us your resume via email to Penzberg@Franz-Wach.de

2.     For further questions you can reach us at the telephone number: 08856 / 60 89 04 0

Franz & Wach Personalservice GmbH
Im Thal 2

82377 Penzberg

E jobs.penzberg@franz-wach.de
T 08856 / 608904-0