Specialist, Quality Assurance Disposition

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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: Myers Squibb Netherlands

Bristol Myers Squibb has been active in the Dutch market for over 50 years employing people across a range of activities and business units in Utrecht The Netherlands.

The Netherlands is also home to our first European Cell Therapy facility located at the Leiden Bio Science Park the largest life sciences cluster of The Netherlands. This new state of the art facility is focused on commercial manufacturing with capabilities for multi-product Cell Therapy manufacturing. You can become part of this exciting journey. Check out this video if you want to know more about it!

The Netherlands has everything it takes to become the medicines hub of Europe the so-called Boston by the North Sea. As we continue to expand our footprint by building this new site we are looking to grow our team.

Would you like to become an important chain in our worldwide network to bring this new personalized treatment to patients suffering from blood cancer Join us and be a game changer!

For more information about Bristol Myers Squibb Netherlands visit us at or Summary

The Specialist QA Disposition is responsible for supporting quality and disposition activities at the Cell Therapy Facility (CTF) in Leiden The Netherlands in accordance with Bristol Myers Squibb (BMS) policies standards procedures and Global current Good Manufacturing Practice (cGMP). Functional responsibilities include performing operational and timely preparation of disposition inputs associated to materials intermediate and drug product prior to release and providing input in the systems impacting disposition i.e. SAP ERP and CELabs LIMS System.

Duties/Responsibilities

• Executes Disposition support activities in alignment with all pertinent Standard Operating Procedures (SOPs).
• Ensures pertinent SOPs are available and present when executing disposition support tasks
• Prepares intermediate drug product and incoming materials disposition documentation and deliverables per SOPs.
• Reviews disposition documentation and deliverables to support disposition of materials and batches within the inventory management systems (IMS) and Enterprise Resource Planning (ERP) including certificate of analysis analytical and environmental testing deviations genealogy specifications and standards.
• Works in electronic systems such as ERP LIMS Learning Management and Document Management systems.
• Works on assignments of moderate complexity where judgment is required in resolving problems and making routine recommendations.
• Develops maintains or reviews SOPs material specifications training and business processes supporting disposition.
• Coordinates with internal and external stakeholders to troubleshoot concerns and issues as required.
• May own Quality System records such as deviations CAPAs or Change Controls.
• Supports archiving and filing of records and other QA department needs as identified by management.
• Supports continuous improvement projects to improve efficiency of the dispositioning and related business processes.
• Supports internal and external inspections as required.
• Maintains compliance with assigned learning plan.
• Supports integration of newer team members.
• Ensures product quality and compliance by enforcing quality assurance policies and procedures; ensures the required processes procedures and resources are adhered to while performing responsibilities.
• Work is self-directed and requires minimal direction to complete tasks by following work practices lists forms and/or procedures.

Reporting Relationship:

Specialist Quality Assurance Disposition reports into Director Disposition Operations.

Qualifications:

• Proficient computer skills with knowledge of several digital tools like MS Office and ability to learn and work with new software applications.
• Excellent verbal and technical writing skills with ability to prepare written communications and present technical data to management with clarity and accuracy.
• Ability to work in a fast-paced team environment and changing priorities.
• Detail oriented and task focused with ability to meet deadlines and prioritize work.
• Able to work across functional groups and teams to ensure requirements are met.
• Self-motivated and contribute to a positive team environment.
• Confident in making decisions for minor issues and able to recognize Quality issues and solve problems.
• Good social skills. Ability to cooperate and adapt to changing circumstances.
• Good digital skills are required.

Education/Experience/Licenses/Certifications:

• High school diploma/ associates degree required.
• A minimum of 2 years of relevant experience in a regulated environment focused on product quality is preferred

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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.

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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.

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