Associate II, Manufacturing Label and Issuance

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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: .

The Manufacturing Label and Issuance Associate II supports the cGMP Manufacturing operations for the BMS Jump site, including the coordination, issuance, reconciliation, and management of production labels and records. To succeed in this role, you will have a strong attention to detail and an analytical mindset.

Primary responsibilities include:

• Issuing production labels, batch records, and other controlled documents to support manufacturing operations
• Coordination of work activities to support manufacturing
• Follow Policies, SOPs and work instructions to support the document approval process, assign effective dates and training workflows, and document change requests
• Execute the process and procedures for identifying and distributing controlled documents for the site
• Support internal and external audits and regulatory inspections. This may require assisting with document retrieval/organization support during regulatory inspections
• Managing an electronic document system for the Bothell site which includes reviewing and approving procedural documents, and troubleshooting and releasing documents to an effective state
• May write and revise Manufacturing Label and Issuance procedures including participating in the development and roll-out of manufacturing label and issuance tools
• Perform Manufacturing Label and Issuance metric reporting and analysis for the local site data. This may require the use of relational databases and reporting tools to collate and analyze quality data

Basic Qualifications:

• Minimum of 1 year of relevant labeling experience in a cGMP/FDA regulated environment
• Some document management experience
• Strong communication and customer service skills.
• Strong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Document Management System
• Develop and improve label issuance processes to drive operational efficiency
• Must demonstrate the following behaviors consistently: Innovative, proactive, and resourceful; committed to quality and continuous improvement
• Able to prioritize, manage time well, multi-task, and troubleshoot effectively
• Ability to work effectively and collaboratively at a fast pace with cross functional departments to finalize time-sensitive deliverables
• Knowledge of cGMPs and domestic regulatory requirement

Schedule:Sun-Wed 1pm-1130pm

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:

Bothell - WA - US: $ $40.80per hour

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