The Manufacturing Manager oversees clinical trial material production, including staff supervision, facility validation, process development, and technology transfer.
Responsibilities include managing manufacturing of oral solid doses and sterile products, collaborating across departments, ensuring GMP compliance, and handling quality documentation.
The role requires 8+ years in pharma, with strong experience in process validation, tech transfer, and regulatory guidelines, plus 5+ years of management.
Key skills include communication, teamwork, and familiarity with microbiology and sterile manufacturing is a plus.
The position offers competitive salary and benefits, with equal opportunity employment policies.