Job was saved successfully.
Job was removed from Saved Jobs.

Job Details

Bristol Myers Squibb

Compliance Specialist

Equipment/Technology Specialist

Equipment and Facilities Specialist


Bothell, Washington, United States

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 primary focus of the Manufacturing Compliance Specialist, Manufacturing Compliance and Training is to support Manufacturing and ensure Jump Manufacturing inspection readiness. Including assisting with leading and driving the execution of Manufacturing Compliance deliverables according to established policies, procedures, and Current Good Manufacturing Practices (cGMP’s). The Manufacturing Compliance Specialist works with cross functional teams, builds and leads compliance programs and processes, collaborates with stakeholders and management, communicates project status and metrics, supports audits and regulatory inspections, and leads compliance evaluation of regulated activities within Manufacturing.

REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:


Bachelors degree preferred, or equivalent in work experience.


  • 4+ years of experience in a GxP Quality or Manufacturing setting
  • 2+ years of experience working with Quality Systems
  • 2+ years of experience in project and/or program management

Knowledge, Skills, and Abilities

  • Ability to work with management and participate in cross-functional teams across the site
  • Demonstrated proficiency in written and verbal communication at all levels within the organization
  • Partner with manufacturing operations to manage stakeholder relationship
  • Negotiates, collaborates, influences, and actively shares ideas with peers and management
  • Demonstrated ability to effectively manage projects at a self-directed pace
  • Acts with individual integrity and professionalism, and demonstrates ability to influence others to act with integrity and professionalism


Key Responsibilities

  • Builds and leads Compliance Programs and processes including:
    • Manufacturing Inspection Readiness
    • Manufacturing Training Compliance
  • Creates and reports Quality System or Compliance Program metrics
  • Provides updates to management and partners with junior team members on obstacle resolution
  • Supports regulatory agency inspections and participates in audit-readiness activities
  • Identifies and mitigates risks in manufacturing operations that could negatively impact delivery of safe and effective therapies to patients
  • Leads/participates in continuous improvement initiatives as part of BMS Bothell site’s commitment to operational excellence
  • Represents Manufacturing on cross-functional teams, provides stakeholder input, cascades information, and takes ownership of deliverables
  • Responds with a high degree of urgency to departmental and cross functional needs and requests
  • Meets timelines with minimal management oversight or intervention
  • Actively pursues continued learning and development
  • Follows safety requirements, completes safety trainings, and escalates safety concerns


  • Temperature controlled, well lighted environment
  • Must be able to sit for extended periods
  • Typing and computer use for extended periods

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 Visit to access our complete Equal Employment Opportunity statement.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.