Sr. Director, Quality Systems & Compliance

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Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: Summary

The Sr Director Quality Systems and Compliance is a full-time position located at the BMS Bothell Manufacturing Plant (JuMP) located in Bothell Washington. The primary focus for this role is to lead the Quality Systems and Compliance teams to ensure site level Quality Systems (Deviation CAPA Change Control Complaints Data Integrity Quality Risk Management and Document Control) are appropriately designed implemented and measured for cGMP compliance and effectiveness. This position is also responsible for ensuring site compliance to health authority regulations and current good manufacturing practices ensuring site inspection readiness. The position leads the management of health authority (surveillance and pre-licensure) and third-party inspections and audits at the site and ensures implementation maintenance and improvement of site self-inspection program. The position oversees the site data integrity program quality governance management escalations and health authority notifications. The position will work cross functionally across Cell Therapy sites and with global counterparts to align and improve quality systems and processes within Cell Therapy.

Duties/Responsibilities

• Identify and implement Quality Systems risk management principles methods and tools and author appropriate policies procedures and reports and provide guidance to staff.

• Oversee and manage all areas of the Quality Systems at the site (Deviation CAPA Change Control Complaints Data Integrity Quality Risk Management and Document Control) to ensure they are appropriately designed implemented and measured for cGMP compliance and effectiveness.

• Collaborate and contribute to the writing coordination review approval and maintenance of the corporate Quality Systems Risk Management and Data Integrity Policies and associated Standard Operating Procedures (SOPs).

• Works collaboratively with above site Quality Systems functions to ensure compliance with corporate standards and policies. Facilitates the implementation of IT tools that drive effectiveness and efficiency into the business.

• Develop and maintain documentation to track key Quality System and risk management related information and provide reporting to include both quantitative and qualitative information into the Quality reporting system.

• Interface with the Global Learning Management team to ensure all site cGMP training and requirements are met.

• Ensure development maintenance and execution of site self-inspection program.

• Ensure development maintenance and execution of site data integrity program.

• Lead the site document and records management programs ensuring alignment with global standards and policies.

• Lead quality management review (Quality Council) for the site ensuring proper identification and reporting of metrics measuring health of site QMS processes and report into the Pillar Quality Council

• Evaluate and report key performance metrics analyze data and lead improvement initiatives.

• Lead and manage the site inspection readiness process to ensure the Bothell is always inspection ready. This includes preparation for routine surveillance and pre-licensure inspections.

• Drive continuous improvement for effective Quality Systems risk management and data integrity programs and to address recurring issues identified throughout Bothell that impact the overall health of the Quality Systems.

• Lead facilitate coach mentor and provide technical expertise for root cause analysis and improvement initiatives across Bothell functional areas.

• Manage health authority inspections and third party GMP audits at the site which includes interfacing with Health Authority prior to during and at the conclusion of inspections.

• Lead site response and commitment process for observations received from health authority inspection and global quality audits of the site.

• Lead compilation and review of annual product quality review (APQR)

• Support authoring of new product licenses/dossiers

• Communicate significant events that may result in health authority notification product recalls etc. to management.

• Perform health authority reporting and correspondence at the site.

• Track and verify appropriate corrective actions have been implemented documented and align with source event.

• Ensure identification and mitigation of key quality and compliance risks at the site.

• Ensure product risk management documentation/files are maintained.

• Represent the Quality unit at various project meetings and provide quality and compliance input in the resolution of significant quality-related issues.

• Work to develop a high performing team delivering performance at a high degree of accuracy.

• Ensure adequate training of personnel in risk management processes.

• Proactively learn develop and customize methods and techniques (e.g. Six Sigma/Lean FMEA Root Cause Analysis etc.) to improve effectiveness of the Risk Management program.

Specific Knowledge Skills Abilities:

• Extensive knowledge of Health Authority Regulations including FDA EMA and PMDA and rest of world (ROW) as it relates good manufacturing practices for pharmaceuticals and advanced therapeutic medicinal products (ATMPs) including ICH Q10 ICH Q9 and 21CFR Part 11.

• Strong written and verbal communication skills

• Knowledge of document and records management and drug product labeling.

• Innovative proactive and resourceful; committed to quality and continuous improvement.

• Ability to work effectively in a fast paced environment with cross functional departments to finalize time-sensitive deliverables.

• Strong interpersonal and advanced leadership skills.

• Able to manage multiple priorities.

• Strong project planning skills.

• Strong computer skills with MS Office (e.g. Word Visio and Excel) and with Quality Systems (e.g. Document Management System Quality Management System) as well as statistical electronic tools.

Education/Experience/ Licenses/Certifications:

• Bachelors degree within science discipline or related field

• 12 years of experience within Cell Therapy biotech or pharmaceutical industry.

• Experience interfacing with health authorities and managing health authority and third-party audits and inspections.

• Strong experience and understanding of Quality Management System structure and function.

• Experience implementing executing and continuous improvement within deviation change control CAPA quality risk management quality processes and systems.

• Experience in implementation and maintenance of document management and records management processes and systems including electronic systems.

• Experience implementing and maintaining cGMP training program and processes including learning management systems.

• Experience leading Quality professionals and people leaders.

• Proven experience working as a detailed oriented team player with effective planning organization and execution skills.

• Experience with health authority reporting and communications.

If you come across a role that intrigues you but doesnt 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.

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 employees 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 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 structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

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 to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position please visit this page for important additional information: Protection

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