Company

Bristol-Myers Squibb CompanySee more

addressAddressBothell, WA
type Form of workFull-Time
CategoryInformation Technology

Job description

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.
Position Summary
The Engineer IT Labs Systems is a full-time position responsible for supporting the lab systems located in Dexter, Seattle - WA. This role will also support printing in our Quality Control Labs, Manufacturing Operations Labs, and Doc Control in Bothell - WA.
Responsibilities include compliance oversight, the drafting and review of knowledgebase (KBA) articles, maintaining the knowledgebase, printer maintenance, building collaborative relationships, and providing support for Seattle and Bothell lab activities. This position aims to foster synergy among our facilities and strengthen the alignment between both of our sites, the IT department, and the business.
The candidate should have at least 10 years of experience in pharma/biotech with specific expertise in Supply Chain, Manufacturing, and Quality System disciplines. The candidate needs to understand shop floor activities, Good Manufacturing Practices (GMPs), electronic change management, and process automation in addition to prior manufacturing support.
Key Responsibilities
  • Directs, supervises, and enhances multiple facets within the print lifecycle.
  • Build Collaborative relationships between departments; Identify business needs, support the implementation of business solutions, and monitor progress/results.
  • Communicates team vision and priorities while creating a helpful and positive work culture.
  • Verify precise label printing and provide operational guidance to operators.
  • Craft and deploy knowledgebase articles (KBAs) while ensuring their ongoing relevance and accuracy.
  • Lead change management: Provide team with a clear vision of why changes are required and the way they will be implemented.
  • Diagnose and resolve calibration challenges.
  • Compliance with current Good Manufacturing Practices (GMPs)
  • Responsible for assessing talent, staff career development and conducts performance management activities & employee counseling with support from assigned leadership.
  • Creates and maintains a customer-focused environment with regular end-user feedback and customer satisfaction surveys, focusing on business retention, customer service.
  • Facilitates the relocation of printers and associated printing peripherals.
  • Administers data operations across designated locations.
  • Elevates the standard of excellence.
  • Performs periodic monitoring in compliance with Standard Operating Procedures (SOPs)
  • Formulate remedial strategies.
  • Collaborating with the business to gain insights into configurations and label stock requirements.

Qualifications & Experience
  • Bachelor's degree in an engineering or MIS discipline.
  • Must have experience with Manufacturing IT Enterprise Systems and Systems Integration.
  • Must have 10+ years of hands-on experience in a biotech manufacturing and supply chain environment.
  • Understanding of supply chain, manufacturing domains, and supporting technology including manufacturing and supply chain ERP systems (e.g., Oracle, SAP).
  • Working knowledge of regulatory requirements and how they relate to existing and new business systems and practices, primarily GXP.
  • Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE).
  • BA/BS in Computer Science, or other related field OR Equivalent Experience
  • Innovative, proactive, and continuous commitment to quality and continuous improvement.
  • Strong project planning skills.
  • Ability to prioritize multiple and competing priorities.
  • Experience in a GXP (GLP, GMP, or GCP) regulated environment.
  • Strong Computer Skills with MS Office (e.g., Word, PowerPoint, Excel, Outlook).
  • Experience with Manufacturing and/or Quality Processes.
  • Ability to work effectively at a fast pace with cross-functional departments to finalize time-sensitive deliverables.
  • Demonstrates system proficiency and takes responsibility.

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.
Refer code: 7641016. Bristol-Myers Squibb Company - The previous day - 2024-01-04 04:23

Bristol-Myers Squibb Company

Bothell, WA
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