Manager, Clinical Quality Standards

Manager, Clinical Quality Standards Job Description:Company Information:Breakthrough Careers!A career at Millennium comes with something no other company can offer: a community of people with diverse talents and backgrounds, all dedicated to the discovery and development of therapies that can change the world - one patient at a time. Our casual but focused environment fosters the free exchange of ideas, encourages collaborative research, and sparks discovery of innovative solutions in science and business. At Millennium, we're big on results, not formality.Position Summary:The Manager, Clinical Quality Standards Quality Control will work to ensure that quality control is built in to the day-to-day activities of the Medical Division. A primary goal for the Manager of Quality Control would be to help achieve efficient and effective quality control practices across the various functional lines within the Medical Division.Duties and Responsibilities:The Manager, Clinical Quality Standards Quality Control will interact with all the functional groups within the Medical Division to build robust clinical quality standards. This person will lead the Clinical Quality Control Initiative whose goal is to facilitate the identification and implementation of best practices and quality control. As a part of delivering the objectives of the Clinical Quality Control Initiative this person will ensure that quality control is incorporated into the line functions as well as cross-functionally among the Medical Division. This person will also be responsible for setting goals and budgets for these activities. This person will report to the Senior Director of Clinical Quality Standards who will be responsible for Quality Assurance, Clinical Quality Control and SOP/Training.Qualifications:Basic qualifications:Position requires a Bachelor's degree, Master's preferred. The ideal candidate will have at least 3-5 years of industry experience and knowledge in quality principles and have worked in quality assurance, clinical operations, regulatory or safety departments. Preferred qualifications:The candidate should have experience and knowledge of clinical drug development and post marketing activities with a thorough knowledge of GCPs and quality principles. In addition the individual should have a demonstrated ability to facilitate/coordinate/manage projects. Familiarity of regulatory inspections would also be of benefit.In depth knowledge of ICH-GCP, FDA and other international GCP-regulations is a plus.Excellent written and verbal communication skills are also a plus.Click here to immediately applyWant to learn more about us? Years of Experience Required: 3-5 YearsExpected Travel Time: None Searchable Keywords: SAS / gj-moExpected Travel Time: None Company: Millennium Pharmaceuticals, Inc. Contact: Recruiter Email: Apply by Email Address: 02454 Reference Code: 14467.26412.5425BR Company: Millennium Pharmaceuticals, Inc. Status: Full Time, Employee Job Category: Biotech/R&D/Science