Information Technology Sr. Specialist

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

The IT Sr. Specialist will be responsible for ensuring quality and promoting efficiency of general IT, systems, and projects at Bristol Myers Squibb, Bothell, WA. This individual will be experienced working with multiple business units and finding solutions. The individual will also occasionally be called upon to support software release activities, investigations, and providing coordination around complex projects. The individual will support projects at Juno’s current multi-product clinical facility in Bothell, WA with potential to support future manufacturing capacity in additional locations.

Responsibilities include:

• Execute Development and implementation of new capabilities across the Manufacturing systems based on requirements and developed software solutions.
• Leads and assists in Quality Assurance related projects and day to day quality activities as needed
• Develops plans for team activities to include quality compliance strategy to achieve agreed targets, and effective planning
• Support Deviations, CAPA and Change Controls
• Writes and/or reviews/approves investigations, cGMP documents, processes, etc. in a thorough and timely manner
• Participate in facility operational meetings to ensure facility reporting needs are met
• Work with subject matter experts to keep the site inspection-ready, organizing resources and materials

Education:

Bachelor’s degree or equivalent experience

Experience:

3-5+ years relevant industry experience Strong communication and collaboration skills. Experience working within electronic document management systems/quality management systems for regulated industries Technical writing competency and GMP procedure writing.

Key Responsibilities

• Support Deviations, CAPA and Change Controls
• Leads and assists in Quality Assurance related projects and day to day quality activities as needed
• Internally collaborate with IT and externally with other Cell Therapy sites and global IT.
• Execute Development and implementation of new capabilities across the Manufacturing systems based on requirements and developed software solutions.
• Participate in facility operational meetings to ensure facility reporting needs are met

WORKING CONDITIONS :

Office environment, seated majority of time. Must be able to move equipment (up to 25lbs).

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.

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.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

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