Glatt Group
We are a leading global supplier of integrated processing solutions for customers in pharmaceuticals, food processing, feeds, and fine chemicals. Our products and services are known for reliability and quality worldwide. About 3,000 employees work for Glatt across more than 15 companies and offices worldwide. For our site in Ramsey, NJ (USA), we have an immediate opening for a
Head of Pharmaceutical Development
Essential Job Functions:
Lead and direct formulation and process development scientists and activities related to client engagements. The primary responsibility is to ensure client success through leadership, planning, and execution of projects. Manage teams that develop and formulate products and processes to meet client needs, including product functionality, implementation timing, and clinical batch production through process validation. Coordinate site functions and development teams to address client-specific needs. Oversee and mentor pharmaceutical experts and scientists, develop scientific strategies to attract new clients, and supervise validation activities. Qualifications:
Minimum of 10 years of experience in pharmaceutical formulation development, process engineering, and validation with a successful track record. Master’s Degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field; PhD preferred. Decisive with ownership and integrity. Strong leadership, management, and problem-solving skills with experience leading multidisciplinary teams. Excellent communication skills. Organized, self-motivated, with a passion for the industry. Hands-on process engineering and validation experience, especially in solid oral dosage forms. Knowledge of regulatory requirements including cGMP, FDA, ICH guidelines, and regulatory filings (NDA, ANDA, 505(b)2, IND). Strong business acumen and strategic thinking to support innovation and growth. Responsibilities:
Prioritize work, provide leadership, and ensure alignment with industry trends and company goals. Oversee planning, execution, and monitoring of client projects, ensuring quality and timelines. Support business development through scientific outreach, client visits, and training seminars. Engage with clients to understand needs and maintain relationships for satisfaction. Mentor and develop scientific teams, fostering collaboration and innovation. Supervise validation activities. Provide technical guidance in formulation, process optimization, and scale-up. Develop standards ensuring compliance with industry and regulatory requirements for filings. Collaborate across departments to support drug development programs and technology transfer. Assist in scoping, forecasting, and billing for client work. Drive process improvements and innovation initiatives. Identify and mitigate project risks, ensuring clear communication with clients. Stay informed on industry trends and emerging technologies to support business growth. Salary range: $150,000 - $200,000 Join us for an interesting and responsible role in a successful, renowned company. We look forward to your online application. Applications via the online portal only can be considered. Glatt Air Techniques Inc., Human Resources, 20 Spear Road, Ramsey, NJ 07446, USA
www.glatt.com
#J-18808-Ljbffr
Essential Job Functions:
Lead and direct formulation and process development scientists and activities related to client engagements. The primary responsibility is to ensure client success through leadership, planning, and execution of projects. Manage teams that develop and formulate products and processes to meet client needs, including product functionality, implementation timing, and clinical batch production through process validation. Coordinate site functions and development teams to address client-specific needs. Oversee and mentor pharmaceutical experts and scientists, develop scientific strategies to attract new clients, and supervise validation activities. Qualifications:
Minimum of 10 years of experience in pharmaceutical formulation development, process engineering, and validation with a successful track record. Master’s Degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field; PhD preferred. Decisive with ownership and integrity. Strong leadership, management, and problem-solving skills with experience leading multidisciplinary teams. Excellent communication skills. Organized, self-motivated, with a passion for the industry. Hands-on process engineering and validation experience, especially in solid oral dosage forms. Knowledge of regulatory requirements including cGMP, FDA, ICH guidelines, and regulatory filings (NDA, ANDA, 505(b)2, IND). Strong business acumen and strategic thinking to support innovation and growth. Responsibilities:
Prioritize work, provide leadership, and ensure alignment with industry trends and company goals. Oversee planning, execution, and monitoring of client projects, ensuring quality and timelines. Support business development through scientific outreach, client visits, and training seminars. Engage with clients to understand needs and maintain relationships for satisfaction. Mentor and develop scientific teams, fostering collaboration and innovation. Supervise validation activities. Provide technical guidance in formulation, process optimization, and scale-up. Develop standards ensuring compliance with industry and regulatory requirements for filings. Collaborate across departments to support drug development programs and technology transfer. Assist in scoping, forecasting, and billing for client work. Drive process improvements and innovation initiatives. Identify and mitigate project risks, ensuring clear communication with clients. Stay informed on industry trends and emerging technologies to support business growth. Salary range: $150,000 - $200,000 Join us for an interesting and responsible role in a successful, renowned company. We look forward to your online application. Applications via the online portal only can be considered. Glatt Air Techniques Inc., Human Resources, 20 Spear Road, Ramsey, NJ 07446, USA
www.glatt.com
#J-18808-Ljbffr