Senior Specialist, Operations Training Lead Job at Bristol Myers Squibb

Bristol Myers Squibb Devens, MA 01434

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t 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. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. 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: careers.bms.com/working-with-us.

Key Responsibilities

  • As a QC Team Member it is my responsibility to compete all required tasks compliantly and safely while consistently and intentionally modeling BMS values (Integrity, Accountability, Passion, Urgency, Innovation, and Inclusion).
  • Perform functions to support lab operations such as housekeeping, alarm acknowledgement, reagent preparation, inventory management, material and reagent ordering, sample pickup and discarding, and execution of work orders.
  • Executes routine testing and procedures owned by the QC functional area for an Analyst VI role.
  • Responsible for team scheduling.
  • Will be required to perform data review for most activities
  • Authors revisions to SOPs for managerial review and approval. Will also own document updates.
  • Contributes to and leads simple and complex projects
  • Trains colleagues in the execution of complex tasks.
  • Contributes to change controls and may own as required.
  • Trains on additional procedures and provides support to a broader spectrum of QC responsibilities.
  • Supports, leads, and may review no impact deviation investigations. Support and leads laboratory investigations.
  • Actively and positively learns and participates in Operational Excellence (OpEx) and Continuous Improvement (CI) initiatives in the team. Is self-driven and mentors others.
  • Identifies and escalates challenges & barriers to execution, suggests solutions, and leads remediation.
  • Identifies and escalates method and/or instrument issues. Also supports and leads solutions.
  • Positive, supportive, and actively collaborates both within and outside the team.
  • Is considered a fully independent analyst capable of executing tasks with no supervision


Qualifications & Experience

  • High School Diploma or Equivalent with 5 years relevant experience; OR Associates Degree in a technical, scientific discipline with 3 years relevant experience; OR Bachelors Degree with 2 years relevant experience.
  • Direct relevant experience in the core responsibilities of the role will be considered in lieu of education.
  • Ability to interpret and apply cGMPs, USP, regulatory requirements and industry best practices.
  • Demonstrated experience with basic activities performed within the specific laboratory setting
  • Attention to detail and demonstrate organizational skills.
  • Ability to manage multiple assignments while meeting timelines in a GMP environment.
  • Excellent organizational and critical thinking skills.
  • The incumbent will be doing light to moderate lifting and carrying objects under 15-20 lbs.
  • Occasional weekend coverage.

If you come across a role that intrigues you but doesn’t 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.

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

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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

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.




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