Global Regulatory CMC Author – Submissions Lead

A leading healthcare intelligence organization in Pennsylvania is seeking a Regulatory Affairs CMC Author. This role involves managing regulatory submissions and ensuring compliance with global standards. Ideal candidates should have 3-5 years of regulatory affairs experience in the pharmaceutical or biotech industry, with strong communication skills and attention to detail. The position offers competitive salary and a range of benefits, fostering an inclusive environment focused on work-life balance. #J-18808-Ljbffr