Regulatory Affairs Specialist

Regulatory Affairs Specialist – Piacenza Office Coree S.R.L., the Italian branch of a multinational group headquartered in South Korea and China, is looking for a Regulatory Affairs Specialist to join its Piacenza office . The company is engaged in the development of innovative concepts in the fields of food, food supplements, medical devices, and pharmaceuticals, with a growing focus on probiotic-based medicinal products . Key Responsibilities: Regulatory feasibility assessment for the registration of new products, with a focus on pharmaceuticals and probiotics; Definition of the most suitable regulatory strategy for product development; Preparation of dossiers for submission to regulatory authorities; Ensuring legal compliance of company products (raw materials, labeling, formulations); Issuance of technical specifications, declarations, and supporting documentation; Management of documentation required for registration in foreign markets; Updating and management of international registration portals; ·Keep updated about international food, food supplements, medical devices and drug legislation; Monitoring and interpreting national and international legislation on pharmaceuticals, food supplements, and medical devices; Supporting regulatory compliance of documents and procedures related to clinical trials sponsored by the company; Acting as a liaison with the international corporate teams (China and South Korea) for the exchange of technical and regulatory documentation. Ideal Candidate Profile: Degree in Life Sciences (e.g., Pharmaceutical Chemistry and Technology, Pharmacy, Biology, Chemistry, Biotechnology, or similar); Proven experience in pharmaceutical regulatory affairs (nice to have: experience with probiotics and/or Master's degree in regulatory affairs) Familiarity with regulatory requirements for food supplements and medical devices (flexibility and willingness to work on these topics is appreciated); Strong writing and editing skills with excellent attention to detail; Excellent organizational and time management abilities; Fluent written and spoken English is essential due to frequent interaction with foreign headquarters. Why Join Us: Be part of groundbreaking probiotic development projects in a fast-evolving regulatory environment. Work alongside global teams and play a key role in shaping public health outcomes in Italy and across the EU. Job Offer: Direct employment with the company under the Italian Terziario National Collective Labor Agreement (CCNL Terziario); Salary and level will be based on the candidate's experience and qualifications; Workplace: Piacenza (on-site, full-time). J-18808-Ljbffr

Location: Plasencia, Emilia-Romaña, IT

Posted Date: 8/17/2025