Senior Specialist, Quality Assurance

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. Cell Therapy is one of the most groundbreaking new forms of cancer treatments being studied today. With therapies only in their infancy and BMS’s continued investment in our Cell Therapy capabilities, the growth potential of this science, your career, and the ability to help patients are incredible. The Quality Assurance Senior Specialist position plays a key role in supporting the cGMP quality operations for the Bothell Manufacturing Plant (Jump).  Primary Responsibilities include the review of cGMP Controlled Documents such as SOPs, specifications, completed batch records, material disposition, and manages implementation of required changes to meet cGMP and internal standards. This role directly supports Jump’s release for infusion (RFI) timeline from the date of manufacture and will support all activities for routine clinical and commercial product release at Jump with an emphasis on supporting Manufacturing with a Quality perspective within a regulated cGMP environment.   The primary focus of the QA Senior Specialist role will be to support routine clinical and commercial production to ensure consistent compliance with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused culture at Jump by ensuring documentation is complete, accurate and that Batch records are executed in accordance with approved and effective standard operating procedures and specifications. This Position qualifies for a $10,000 Sign-on Bonus, $5,000 payable within 30 days of the start date, and $5,000 payable following 6 months of continuous employment. Payments are subject to a 1-year repayment agreement from date of payment issue. Applies to external hires only. This is a shift position. The shift is Wednesday - Saturday 1:30pm - 12:00am. QUALIFICATION REQUIREMENTS (Knowledge, Skills and Abilities): Education: Bachelor’s degree in relevant science or engineering discipline is preferred. Minimum of Associates degree and/or equivalent combination of education and experience is required.    Experience: 5-8 years of relevant cGMP experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.    Experience with use of complex research techniques and methodologies like six sigma and Kaizen to improve process/product quality is a plus.    Hands-on experience with batch record review and product disposition.    Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing.    Strong computer skills with Word and Excel and other electronic manufacturing systems.    Detail oriented team player with effective planning, organization, time-management, and execution skills.    Proven experience working on teams where combined contribution, collaboration, and results were expected.    Must exercise accurate judgment and be able to evaluate information critically and decide upon appropriate course of action.    Must be able to correlate events and determine the action plan required to avoid incidents recurrence and apply them.    Extensive experience in Quality Assurance processes.    Ability to work in a high paced team environment.    Strong written and verbal skills.    ROLES AND RESPONSIBILITIES: Review executed batch records to ensure compliance with approved procedures and communicate and resolve discrepancies with manufacturing operators or supervisors.    Conduct Quality on the Floor activities including quality walk-throughs of the production, testing and warehouse locations.    Provide Quality support to Manufacturing personnel on the floor; provide guidance during GMP events and initiation of deviation investigations.    Review deviations, product non-conformities, and GMP investigations to ensure adequate resolution and compliance with current Good Manufacturing Practices (GMPs).    Act as QA Subject Matter Expert (SME) and support cross functional groups on root cause analysis and development of corresponding corrective and preventive actions.    Support the batch disposition process by ensuring that all required documents are accurately and properly completed, including all batch related deviations.    Oversee manufacturing operations during patient material receipt and drug product pack out.    Own department events and minor deviations   May support internal and external audits, including documenting observations and oversee implementation of corresponding CAPAs (Corrective and Preventative Action).    Perform quality review and approval of standard operating procedures     Train and mentor junior associates. If you want to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here with our Cell Therapy team. Full of incredible and dedicated team members, those working on CAR-T and other forms of Cell Therapy are transforming patients’ lives through science. From studying individualized cell lines to making brand new discoveries, this bold and personal discipline allows you to grow your career while making a lasting impact on the field of medicine. Join us today. WORKING CONDITIONS (US Only): While performing the duties of this job, the employee is frequently required to stand; walk; sit; bend; stretch; use hands and fingers, with various manipulations; reach with hands and arms; and effectively communicate with others in the workplace, including the ability to make and promptly respond to audible cues and warnings.  May Work in areas that may have strong magnets.    May work in areas with exposure to vapor phase liquid nitrogen and other chemicals.   Must be able to gown per requirements to enter manufacturing space.   Will be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include, but not limited to safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hairnets, gloves, and hearing protection.   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. BMSCART, Veteran,
LI-Onsite 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 [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.