Director, Manufacturing Legal Counsel
The Director, Manufacturing Legal Counsel at Kyowa Kirin North America will serve as the primary legal advisor for the company's new manufacturing facility in Sanford, North Carolina. This role involves providing comprehensive legal support throughout the site's development, from construction to full operational status, ensuring compliance with all applicable laws and regulations.
Key responsibilities include managing the contracting process for the Sanford facility, encompassing the drafting, negotiation, and execution of agreements related to manufacturing, construction, consulting, equipment, supply, and operations. The counsel will also offer legal guidance on regulatory matters pertinent to pharmaceutical manufacturing, such as compliance with the Food, Drug, and Cosmetic Act, and support Human Resources on employment and employee relations issues specific to the Sanford site.
The ideal candidate will possess a Juris Doctorate from an accredited law school, admission to at least one U.S. state bar, and eligibility for North Carolina in-house registration. A minimum of 4–8 years of legal experience is required, preferably including contracting and legal support for manufacturing, construction, or operations in a regulated industry. Experience in the life sciences sector is preferred but not mandatory.
Kyowa Kirin North America offers a competitive compensation package, including a 401(k) plan with company matching, discretionary profit sharing, an annual bonus program, generous paid time off and holiday schedules, comprehensive healthcare benefits, and various well-being and work/life programs. Additional perks include life and disability insurance, concierge services, pet insurance, tuition assistance, and employee referral awards.
Joining Kyowa Kirin North America means becoming part of a dynamic, patient-centric organization dedicated to delivering innovative medicines in areas of unmet need. The company fosters a collaborative and inclusive culture, providing opportunities for professional growth and development within a rapidly expanding global pharmaceutical company.