Hybrid EU Regulatory Affairs Expert PPE/MDR

ZEISS Group in Castiglione Olona, Italy is seeking a Regulatory Affairs Expert to ensure products meet safety, labeling, and legal requirements across the EU and other markets. The role emphasizes collaboration with global teams and regulatory authorities.You will coordinate approvals, handle incidents and recalls, maintain regulatory records, and support...

Regulatory Affairs Expert Castiglione Olona, Varese (3 days on-site – 2 days smart working) Permanent, Full Time ZEISS is technology and innovation. Founded in Germany in 1846, we're an internationally leading technology enterprise operating in the optics and optoelectronics industries generating more than 10.8 billion Euros in revenue with around 46,000...

Regulatory Affairs ExpertCastiglione Olona, Varese (3 days on-site – 2 days smart working)Permanent, Full TimeZEISS is technology and innovation. Founded in Germany in 1846, we’re an internationally leading technology enterprise operating in the optics and optoelectronics industries generating more than 10.8 billion Euros in revenue with around 46,000...

About The RoleWe are seeking an experienced Regulatory Affairs professional to lead medical devices and combination products regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory pathways for clinical investigations and marketing authorizations, and serve as the key regulatory representative for our global project...

Pay Rate: €30 per hourLocation: Milan, Italy | Hybrid – 3 days onsite per weekContract: Full-timeIndustry: Dental Medical DevicesLanguage: Fluent Italian requiredMeet Life Sciences is seeking an experienced Quality Management System (QMS) and EU MDR Consultant for a full-time contract opportunity within the dental medical device sector in Milan.We are...

Pay Rate: €30 per hour Location: Milan, Italy | Hybrid – 3 days onsite per week Contract: Full-time Industry: Dental Medical Devices Language: Fluent Italian required Meet Life Sciences is seeking an experienced Quality Management System (QMS) and EU MDR Consultant for a full-time contract

Overview As Regulatory Affairs Expert, you ensure ZEISS Sun Lens products meet EU and global requirements, coordinating with regional teams. You will act as the primary contact for EU regulators and manage product approvals, recalls, and safety actions. The role involves maintaining regulatory records, advising other departments, and training staff on...

Regulatory Affairs Expert Castiglione Olona, Varese (3 days on-site – 2 days smart working) Permanent, Full Time ZEISS is technology and innovation. Founded in Germany in 1846, we’re an internationally leading technology enterprise operating in the

Regulatory Affairs Expert Castiglione Olona, Varese (3 days on-site – 2 days smart working) Permanent, Full Time ZEISS is technology and innovation. Founded in Germany in 1846, we’re an internationally leading technology enterprise operating in the optics and optoelectronics industries generating more than 10.8 billion Euros in revenue with around...