EU Pharma Regulatory Specialist & Compliance Expert

A leading consulting firm is seeking per diem pharmaceutical consultants proficient in English and one other European language. Ideal candidates should have a B.S. in life sciences or engineering, with over 10 years of experience in regulatory compliance, quality assurance, and FDA regulations. Responsibilities include performing GMP audits, managing regulatory compliance evaluations, and contributing to the drug approval process. Strong communication and project management skills are essential.
#J-18808-Ljbffr