Specialist QC Analytical Technical Support

Working 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 rich in diversity. 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.In this role you will perform super user activities for the laboratory computerized systems, including Master Data Management activities, and associated GMP document updates. This position will act as a Super User providing support and training to End-Users of the QC laboratories as well as supporting investigations and resolution of issues. In addition, this position will support activities related to acquisition and qualification of new equipment, investigation and troubleshooting of analytical and equipment issues as well as introduction of new products to the QC laboratories. The Specialist will report to the Sr. Manager QC Analytical Tech Support.Key ResponsibilitiesSuper user of laboratory computerized systems:Performs master data management activities in computerized systems (e.g Empower, Dissolution Workstation, Tiamo, etc.), including new methods set up. Writes and executes verification protocol for custom calculations.Performs audit trail reviews and assures adherence to data integrity principles.Assists QC End Users with software issues.Provide end user training and on-the-job training for new employees where required.Updates and reviews associated GMP documents and procedures.Support change controls for QC software.Supports risk assessments.Equipment lifecycle activities.Supports acquisition and qualification of new analytical equipment.Performs feasibility experimental work as needed.Supports decommissioning of analytical equipment.Supports laboratory investigations in case of equipment-related deviations.Supports End-User with equipment troubleshooting.Deviation and Laboratory Investigation SupportSupports system-related deviations.Supports laboratory investigations associated to equipment deviation.Supports with corrective and preventive actions definition.Promotes safe practices and behaviorsReports immediately incidents to Environmental Health and Safety department, participate in investigations and identify measures to prevent similar accidents in the future.Demonstrate Bristol Myers Squibb values.Performs other tasks as assigned.Qualifications & ExperienceEducation and ExperienceFederal Certificate of Capacity as Laboratory Technician or BS degree in Life Science, Chemistry, or relevant scientific discipline or equivalent combination of education, training and experience.Minimum 4 years relevant work experience required, preferable in a regulated pharmaceutical environment.Scientific and practical knowledge of analytical techniques (e.g., chromatography techniques (High-performance liquid chromatography, Ultra-performance liquid chromatography, Gas chromatography), Dissolution, UV/VIS, and IR techniques).Previous experience of laboratory equipment qualification is preferable.Required Competencies:  Knowledge, Skills, and AbilitiesGood scientific knowledge of chromatography techniques (HPLC, UPLC, GC), dissolution, Karl Fischer, and spectroscopic techniques.Exceptional knowledge of LIMS and Empower applications.Advanced knowledge and interpretation of cGMP, ISO, FDA, MHRA and Pharmacopeia requirements, and good documentation practices.Advanced knowledge of Data Integrity principles, familiar with audit trail review requirements.General computer literacy including MS Office (Word, Excel, PowerPoint, Outlook)Effective verbal communication skills, ability to interact with different levels of the organization and departments.Effective technical writing skills, experience writing GMP documents (procedures, protocols, plans and reports).Proven analytical, problem-solving, and continuous improvement skills.Proven time management skills and a strong attention to detail.Ability to work independently and compliantly.Physical ability to perform tasks that may require prolonged standing, sitting, and other activities necessary to perform job duties.Fluent in English or French and professional command of the second language (written and verbal).If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.