Vacancy expired!
Key responsibilities: Act as core team member responsible for coordinating and identifying Regulatory and Compliance Remediation activity plans related to product transfer. Basic Qualifications and Skills needed Degree in Science or Engineering based discipline, laboratory experience a plus Familiarity with Change Management requirements, and Processes related to Compendial methods remediation, validation/qualification for manufacturing, and Quality and technical risk management tools. Relevant Drug Product Technical Experience related to processing and manufacturing pharmaceutical products. Excellent Communication and presentation skills. Relevant experience with manufacturing operations for Sterile Injectable Drug Products. Relevant skills to gathering data from multiple sources and summarizing into simple, well organized documents Ability to be flexible and manage multiple deadlines Work independent to meet deadlines within team goals Documentum, Doc-U Sign and Track-wise experience preferred Additional Sills:
Vacancy expired!