Director, Quality Control

Career Areas Career Stories Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Careers Home Life at BMS Career Areas Student Opportunities Events How We Recruit Career Stories Search this site Join Talent Community Candidate Login English English Italiano Español Français Português Norsk Deutsch 日本語 Bahasa melayu 中文 (简体) 中文 (繁體) 한국어 ภาษาไทย Nederlands Polski Yкраїнська Hrvatski Ελληνικά Magyar čeština Türkçe Pусский Haitian עברית Brazilian Português Dansk Suomi Svenska Français (Canada) Português (Portugal) Single PositionView All JobsDirector, Quality ControlLeiden – NLApply NowFind out how well you match with this jobUpload your resumeJob descriptionLife at BMSWorking with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position summary The Director QC is responsible for QC laboratory operations to ensure timely completion of testing (e.g., drug product, intermediates stability, raw materials and microbiology/EM) that is performed in compliance with regulatory agencies, cGMPs, and other company policies and procedures. Responsible for managing the QC budget. The Director QC is also responsible for on time closure of Lab investigations and associated CAPA’s. Oversee management and scheduling of multiple teams with varying functions and goals within the department.ResponsibilitiesDirects QC laboratory to ensure timely completion of testing (e.g., drug product, intermediates, stability, raw materials) that is performed in compliance with regulatory agencies, cGMPs, and other company policies and procedures.Defines departmental roles and accountabilities. Hires, integrates, and develops high quality talent capable of delivering against the department’s goals and objectives.Establishes and communicates performance objectives for QC staff that are consistent with the business unit and Quality goals. Defines and monitors performance measures, provide developmental feedback and coaching, and creates a collaborative environment that attracts, develops, and retains the best talent. Accountable for lifecycle management of analytical methods and technology within the QC laboratory.Directs and participates in continuous improvement efforts to drive business efficiencies (e.g., TAT improvements, COGM reductions).Directs programs which assure the proper operation and maintenance of laboratory equipment and the timely data analysis and reporting of trends.Participates in the site team, which prepares for, hosts, and responds to regulatory inspections, reviews, and approvals of the facility and products.Accountable for on time completion of quality records within the QMS.Accountable for completion of Annual Product Quality Review and periodic investigation trending reports.Verifies compliance with applicable BMS Policies and Procedures and ensures consistency with other site procedures and/or specifications.Responsible for managing the QC...