Associate II, Manufacturing Labels

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. 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:

Position Summary

This role is part of the Bothell Manufacturing Logistics & Services team and will focus supporting cGMP Manufacturing Operations for the BMS Bothell site, including the coordination, issuance, reconciliation, and management of production labels and records.

Functional responsibilities include all batch label and documentation control activities for Cell Therapy Operations (CTO), including performing and maintaining a GMP compliant clinical and commercial batch documentation and label issuance and control process.

Duties/Responsibilities

• Issuing production labels, batch records, and other controlled documents to support manufacturing operations.
• Coordination of work activities to support manufacturing.
• Managing an electronic document system for the Bothell site which includes reviewing and approving document change requests, troubleshooting, and releasing documents to an effective state.
• Execute operations as outlined in Standard Operating Procedures (SOPs) and work instructions.  
• Executes transactions and process in all applicable electronic systems.
• Controlled document & Deviation authoring.
• Demonstrate a strong practical knowledge in their work.
• Can represent department in departmental collaborations.
• Contributes to BMS culture and values.
• Solve technical problems by taking new perspectives using existing solutions.
• Perform all tasks in a manner consistent with the safety policies, SOPs, quality systems, and GMP requirements
• Complete training assignments to ensure the necessary technical skills and knowledge
• Train for proficiency in process systems and some supporting business systems
• Train others on SOPs, Work Instructions to successfully complete manufacturing operations
• Identify and propose innovative solutions.
• Role models the culture of compliance.

Reporting Relationship

Reports to Supervisor, Manufacturing Labels & Issuance.

Qualifications

Qualifications

• Extensive knowledge of SOPs and cGMPs and the know–how to work and manage within a regulatory environment.
• Demonstrates aptitude for engineering principles and manufacturing systems.
• Adaptable to a fast paced, complex, and ever-changing business environment.
• Quality Systems for Deviation, SOP revisions/creation, CAPA Management. 

Education:

• Associate or bachelor's degree in related field is preferred.
• A minimum high school diploma and/or equivalent combination of education and experience is required.

Experience:

• 1+ years of experience in a cGMP environment and understanding of manufacturing best practices.    

Shift Options:

Front Half PM - 1:00pm to 11:30pm

Back Half AM - 6:00am to 4:30pm

Back Half AM - 6:00am to 4:30pm

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.

Compensation Overview:

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