EXECUTIVE REGULATORY AFFAIRS

Role Overview: As a Regulatory Affairs professional, you will be responsible for supporting the regulatory affairs function on finished dosage forms in the pharmaceutical industry. Your role will involve ensuring compliance with current Regulatory and GMP requirements such as US FDA, EU GMP, and PIC/s. Key Responsibilities: - Support regulatory affairs function on finished dosage forms - Ensure compliance with current Regulatory and GMP requirements (US FDA, EU GMP, PIC/s) - Demonstrate strong initiative skills, working independently and as part of a team - Communicate effectively in English - Utilize advanced Microsoft Office skills (Word, Excel, PowerPoint, Outlook) Qualifications Required: - Masters or Bachelors degree in Science or Pharmacy - Minimum of 7-10 years of experience in a similar function in the pharmaceutical industry Additional Details: N/A,