Senior Specialist, QC Systems and Support

Working with Us

Challenging. Meaningful. Life-changing. Bristol Myers Squibb offers work across departments, with opportunities to grow alongside high-achieving teams. Read more about our approach to working with us : careers.bms.com / working-with-us.

Bristol 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 home to our first European Cell Therapy facility, located at Leiden Bio Science Park, focused on commercial multi-product Cell Therapy manufacturing. You can become part of this exciting journey. Check out this video to learn more.

The Netherlands aims to become the medicines hub of Europe. As we expand our footprint with this new site, we are looking to grow our team and invite you to become part of our worldwide network to bring this new personalized treatment to patients suffering from blood cancer.

For more information about Bristol Myers Squibb Netherlands, visit bms.com / nl or careers.bms.com / nl.

Position Summary

The Sr. Specialist QC Systems and Support facilitates operations of the Systems and Support group for the Quality Control department. Key responsibilities include management of samples, equipment, and materials (incoming goods and laboratory supplies). The group also oversees electronic systems used for inventory management and scheduling within the QC department.

This role is stationed in Leiden and reports to QC management. The role is on-site.

Duties / Responsibilities

• Manage QC equipment lifecycle tasks in collaboration with QC laboratories, Site Engineering, Facility Services, and other departments.
• Keep laboratory equipment in cGMP state, including validation, calibration, maintenance, and repairs.
• Provide basic and first-line equipment troubleshooting.
• Maintain electronic equipment database, records, logs, and status metrics; apply status labels in accordance with GMP and written procedures.
• Support development and maintenance of QC scheduling and planning systems.
• Develop, maintain, and implement updates to ensure scheduling reflects current practices.
• Support training of peers in QC systems and processes and procedures.
• Perform document revision, project, CAPA, and related tasks and / or continuous improvement efforts.
• Initiate and complete Deviations and Change Controls where needed.
• Perform other tasks to support the QC laboratories.

Specific Knowledge, Skills, Abilities

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Why You Should Apply

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, apply anyway. You could be one step away from work that will transform your life and career.

On-site Protocol

BMS has an occupancy structure that determines where work is conducted. Roles are site-essential, site-by-design, field-based, or remote-by-design. The assigned occupancy type is based on role responsibilities.

Site-essential roles require 100% onsite, site-by-design roles may be hybrid with at least 50% onsite, and field-based / remote-by-design roles require travel and meetings as directed.

BMS is committed to accessibility; applicants can request reasonable workplace accommodations during recruitment and employment. For inquiries, contact Visit careers.bms.com / eeo-accessibility for our EEO statement.

BMS encourages vaccination and boosters for Covid-19, and will consider applicants with arrest or conviction records as permitted by law.

If residing in Los Angeles County, visit careers.bms.com / california-residents for important additional information. Data collected in role applications will be handled per applicable data privacy policies and regulations.

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