Warner Chilcott is a global specialty pharmaceutical company currently focused on the gastroenterology, women's healthcare, dermatology and urology segments of the North American and Western European pharmaceuticals markets. Headquartered in Dublin, Ireland, Warner Chilcott has employees in 12 countries in North America and Western Europe. The Company's manufacturing facilities are located in Puerto Rico, Northern Ireland and Germany. Warner Chilcott is listed on the Nasdaq Stock Exchange and trades under the symbol WCRX. We currently have an opportunity available.
The individual will be responsible for the following activities:
Supervise and coordinate the activities of workers engaged in the manufacturing of tablets/ semi-solids. Ensure that all products manufactured in the department are in accordance with GMP’s and established procedures. Recommend improvements to manufacturing processes. Assist the Departments manager in the development of budgets, cost standards, and capital investment plans.
*Bachelor’s degree in Pharmacy, Chemistry, Engineering, Management or any other related in the field.
*Five (5) years of experience in manufacturing in pharmaceutical industry in Solid Dosage Processes.
*Knowledge of GMP’s, SPC, and safety regulations
*Supervisory background required
*Fully bilingual (English and Spanish). Requires reading professional literature and technical manuals; speaking to groups of employees, other public and private groups; writing documents and complex reports in English and Spanish.
*Computer knowledge, including word processing, presentation, worksheets and electronic mail
*Knowledge of cGMP’s, SPC and safety regulations
*Ability to establish and maintain effective working relationships at all levels
*Ability to interpret technical reports for implementation of processes and practices
Warner Chilcott PLC develops and markets branded prescription pharmaceutical products in the United States. The Company's primary area of...