Systems Development, Integration & Operations, QC Systems

Job description

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. 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. Key Responsibilities · Accountable for the controlled production support and lifecycle management for GPS Quality Systems applications. · Accountable for delivery of committed business outcomes of digital capabilities implemented within the respective area. · Work with a dynamic team to oversee the design and implementation of custom /cots applications. · Collaborate directly with the business clients, IT Business Partners and other IT functions on delivery of digital capabilities. · Monitor IT service provider resource consumption, review demand and change requests for support work related to COTS/custom applications. Qualifications & Experience: Bachelor’s degree on the Sciences (Biology, Chemistry, etc.) or Computer Science. 5+ years overall work experience in Information Technology environment for delivery and support of manufacturing and business applications in a regulated environment. 3-5 years of experience as a user for Quality Systems applications in a lab will also be considered. Must have knowledge of software development lifecycle (SDLC) and of computer systems validation (CSV) Experience working in large and/or complex IT programs, preferably within the quality control domain. Demonstrated ability to use structured problem solving and available tools to quickly evaluate problems, identify root causes, create action plans, assess impact and develop resolution options Deep analytical skills and logical thinking to identify and resolve technical issues. Knowledge of cGxP and 21CFR Part11 standards. Experience using IT Service Management tool such as ServiceNow. Ability to design, author, edit and execute test scripts using automated testing tool such as ALM. Track record of innovation, results, and ability to collaborate and affect change across functions. Strong time management skills with the capacity to meet deadlines and prioritize work from multiple projects. Excellent oral and written communication skills, and relationship building skills to establish trust and rapport with the business teams. Strong sense of responsibility, accountability, and integrity. Desired Candidate Characteristics: · Have a strong commitment to a career in technology with a passion for healthcare · Ability to understand the needs of the business and commitment to deliver the best user experience and adoption · Able to collaborate across multiple teams · Demonstrated leadership experience · Excellent communication/collaboration skills · Innovative and inquisitive nature to ask questions, offer bold ideas and challenge the status quo · Agility to learn new tools and processes · 2-5 years’ experience in IT with demonstrated success in supporting and delivering Laboratory Information Management Systems (LIMS), Quality systems / applications and other COTS applications like SmartQC. Ideal Candidates Would Also Have: · Deep analytical skills and logical thinking to identify and resolve technical issues. · Experience creating complex custom solutions using coding languages and understanding of different systems used in laboratory. · Ability to work independently on most deliverables. 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. Compensation Overview: Devens - MA - US: $108,650 - $131,655 New Brunswick - NJ - US: $98,770 - $119,686 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: Health Coverage: Medical, pharmacy, dental, and vision care. Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. ​Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. *Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program. 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 a supportive culture, promoting global participation 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 BMS has an occupancy structure that determines where an employee is required to conduct their work. This struc