Project Specialist, QC Chemistry

Working with Us Challenging. 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 Project Specialist, Quality Control Chemistry Location: Phoenix, Arizona Shift-1st.- 6am.-2pm. Qualifications & Experience Bachelor’s degree preferred, preferably in scientific field. 1-3 years’ experience preferred. An equivalent combination of education and experience may be substituted. Ability to work with moderate supervision. Desired Competencies Intermediate knowledge of related technical skills required for analytical chemistry. Comprehensive understanding of processes and instrumentation. Intermediate knowledge of cGMP, OSHA, DEA, USP, EP, and JP; ability to deal appropriately with regulatory agencies. Intermediate skills with project management tools and tracking data Key Responsibilities Perform testing of raw material, in-process, finished product and stability samples. Perform various wet chemistry and analytical chemistry methods. Perform high complexity analytical testing. Follow methods and procedures, with strict adherence to cGMP documentation requirements. Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner. Assist in troubleshooting technical problems and inform management as appropriate. Perform peer review of testing data. Review all data in accordance with applicable procedures and cGMP requirements. Complete all review in accordance with required release timelines. Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required. Complete necessary training to become a qualified trainer. Manage projects involving technical documents, interdepartmental and global cooperation, and CAPA, and investigation/deviation tasks. Manage and facilitate multiple large and small-scale projects, such as lab equipment procurement, phased technical system implementations, and process development. Draft and review technical documents, such as SOPs and protocols. Communicate effectively with management regarding task completion, roadblocks, and needs. Assist in the development and implementation of corrective actions. Participate in housekeeping performance and audits. Prepare various solutions needed to support method performance, for example, mobile phase, needle wash, etc. Review status of supplies and reagents to ensure items are ordered as needed. Performs other tasks as assigned. Required Knowledge, Skills and Abilities Basic experience with analytical laboratory techniques Basic project management skills Basic proficiency in Microsoft Word, Outlook, and Excel Basic knowledge of laboratory safety practices Basic knowledge of electronic document management systems Basic knowledge of cGMP, compendia; ability to deal appropriately with regulatory agencies Intermediate Personal Computer skills Intermediate math skills Intermediate written and verbal communication skills Intermediate knowledge of technical skills required for analytical chemistry Intermediate strategic thinking and problem solving Intermediate GMP documentation skills Strong attention to detail Ability to use Personal Protective Equipment effectively Ability to collaborate with peers on day-to-day tasks and more technical tasks; cooperative and works well with a team Ability to communicate effectively with peers, department management, cross-functional director-level management Ability to understand and follow SOP, test method, and cGMP requirements; uses good judgment and follows procedures accurately and completely Ability to use and troubleshoot instrumentation and instrument software Ability to interpret/write technical documents Ability to make presentations in department setting Actively seeks opportunities to learn Ability to pass an initial full physical with annual monitoring Working Conditions This position is a First Shift role with expected hours: (M – F, 6:00 am – 2:00 pm) This position requires regular medical surveillance and may require incumbent to wear a respirator or gown. The incumbent must be able to distinguish colors and possess correctable vision to 20/20, annual eye exam is required. The incumbent must analyze numerical values daily. The incumbent will be working in a laboratory setting up to 6 hours per day. The incumbent will occasionally be working around hazardous materials to include chemical agents up to 6 hours per day. The incumbent often works for extended periods alone, up to 8 hours per shift. Travel requirements- travel not expected. On-site Protocol Physical 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. COVID-19 Information To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S. BMS is dedicated to ensuring that people with disabilities can perform complex functions through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. 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. BMSBL
LI-Onsite 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 Careers With 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 Protocol Physical 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. COVID-19 Information To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S. BMS is dedicated to ensuring that people with disabilities can perform complex functions through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. 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.