Senior Director, Analytical Excellence

Not Interested
Bookmark
Report This Job

profile Job Location:

Seattle, OR - USA

profile Monthly Salary: Not Disclosed
Posted on: 2 days ago
Vacancies: 1 Vacancy

Job Summary

Working with Us
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

TheSr. Director Analytical Science and Technology (ASAT) Analytical Excellenceis responsible for defining and driving strategic Quality Control (QC) Excellence programs across BMSs global cell therapy role will be responsible for driving alignment and harmonization of analytical method performance execution and efficiency improvements partnering closely with QC Quality and Analytical Development stakeholders. The individual will champion initiatives that improve analytical method performance facilitate best-in-class operational practices and optimize the use of analytical instruments and software platforms.

Duties/Responsibilities

  • Develop implement and continuously improve the QC Excellence strategy for global QC sites focusing on method harmonization performance optimization and operational efficacy

  • Lead cross-functional teams to establish standardized procedures tools and metrics for routine QC testing

  • Partner with site QC Quality (GPQ and QA) and ASAT functions to assess current practices identify gaps and drive alignment

  • Champion data-driven decision-making and continuous improvement principles for analytical method execution

  • Own and evolve business processes for QC-related analytical instruments and software systems coordinating with IT and site SMEs

  • Benchmark industry best practices and implement innovative approaches to process efficiency regulatory compliance and quality improvement

  • Monitor performance indicators compliance metrics and operational dashboards using findings to inform global improvement initiatives

  • Prepare and present strategic plans performance updates and improvement proposals to executive leadership

  • Mentor and develop team members fostering a high-performance and collaborative culture

  • Ensure robust change management and stakeholder engagement throughout all initiatives

  • Foster a culture of excellence and accountability for cell therapy across all partners and stakeholder.

Reporting Relationship

Reports to the Executive Director Analytical Science and Technology

Specific Knowledge Skills Abilities:

  • Extensive experience in analytical science QC operations or method lifecycle management within the pharmaceutical/biologics industry; leadership at a multi-site/global level preferred

  • Demonstrated expertise in analytical method development validation transfer troubleshooting and routine QC operations

  • Proven track record of leading complex cross-functional global initiatives preferably in operational excellence or continuous improvement roles

  • Deep understanding of analytical instrument platforms and enterprise software systems used in QC testing

  • Strong project management and organizational skills able to coordinate multiple initiatives across diverse stakeholders

  • Exceptional communication influencing and stakeholder engagement abilities

  • Data analytics competence with ability to analyze complex data sets and drive improvement actions

  • Sound knowledge of current GMP regulatory expectations and quality management systems

  • Change management expertise with experience implementing harmonization or transformation programs at scale

  • Collaborative leadership style; ability to inspire and drive teams towards a common vision

  • Strategic thinker with a results-driven proactive approach

  • Demonstrated decision making and problem-solving capabilities relative to Quality compliance technical considerations and regulatory requirements are required.

  • Ability to build strong trusting relationships lead large/complex teams and work across divisions diverse business backgrounds and cultures.

  • Excellent communication and interpersonal skills with the ability to interface with a broad range of internal and external stakeholders at all levels of the organization.

  • Demonstrates a consistent ability to achieve objectives and maintains a proactive approach to tasks.

Education/Experience/ Licenses/Certifications:

  • MSc or BSc in Cell Biology Molecular Biology Bioengineering or equivalent with 15 years of relevant experience in QC operations or commercial manufacturing or PH.D in Cell Biology Molecular Biology Bioengineering with minimal of 10 years of experience

  • Preference will be given to candidates with Cell Therapy experience

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.

Compensation Overview:

Devens - MA - US: $230950 - $279861 Seattle - WA: $237430 - $287710

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

We will never request payments financial information or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R: Senior Director Analytical Excellence

Required Experience:

Exec

Working with UsChallenging. 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 breakthrou...
View more view more

Key Skills

  • Gas Chromatography
  • Laboratory Experience
  • Analytical Chemistry
  • FDA Regulations
  • High-Performance Liquid Chromatography
  • Spectroscopy
  • Research & Development
  • Teradata
  • GLP
  • Alteryx
  • cGMP
  • Analytics

About Company

Company Logo

Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more

View Profile View Profile