Bristol Myers Squibb

Bristol Myers Squibb

Specialist, QC Systems and Support – QC Planner

Leiden – NL, NL · Mid

Sponsorship not specifiedDetected 3 days ago
AccessibilityExcelSAPGMPCollaborationProblem SolvingMicrosoft OfficeSharePoint

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odds of building a lasting career here

38Risky
Cap-exempt (no lottery)0
Sponsors this role85
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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Employer immigration record

from this employer's Department of Labor filings

Green-card filing pattern in this occupation

Context, not a finding about this posting: of this employer's 44 green-card filings in this occupation, 100% were for a worker who already held the job.

Green-card follow-through: 41%

Of 27 labor certifications old enough to have been used, 16 expired without the employer filing the next step. Median time from filing to decision: 475 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Reported a layoff in this occupation

In a green-card filing decided 2026-01-29, this employer stated it had laid off workers in Biostatisticians (NJ) during the preceding six months. 3 such filings on record.Describes the period before that filing, not necessarily today. Unlike WARN notices this is occupation-specific and federal.

Files H-1B transfers

29 transfer filings in the last year, covering 29 workers. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • The Specialist QC Systems and Support - QC Planner supports reliable and efficient Quality Control (QC) laboratory operations by maintaining and improving the systems used to plan and schedule laboratory testing, coordinating planning activities, and aligning schedules with business and operational priorities.
  • The role maintains short- and long-term workload forecasts, planning data, user access, system interfaces, and reports; identifies capacity and scheduling risks; and helps ensure planning can continue during system or data disruptions.
  • The position also resolves system issues, supports user acceptance testing, implementation, and validation of system changes, uses planning data to identify performance improvements, and trains users in QC planning tools and processes.

Responsibilities

  • Maintain, optimize, and update QC scheduling and planning systems to reflect current laboratory practices.
  • document decisions and actions, identify capacity or schedule conflicts, and escalate risks to testing, disposition, stability commitments, or laboratory readiness.
  • Maintain short- and long-term forecasts, including planning for stability studies, other studies, and material/product disposition.
  • Manage planning tool data, user access, master data, interfaces, and reporting capabilities.
  • Resolve planning tool issues and document lab floor feedback to support continuous improvement.
  • Support UAT, implementation, and validation of QC planning system releases and enhancements by evaluating functionality, documenting defects, and providing business-user feedback.
  • Maintain contingency plans and approved fallback processes to ensure QC planning continuity during system, interface, or data disruptions.

Requirements

  • Bachelor's degree in a relevant scientific, computer or engineering program area.
  • Proficient knowledge of a lab system such as Smart QC, LIMS, SAP, etc., understanding of system interfaces and impact of changes to each other.
  • If this posting is missing required information required by local law or incorrect, contact BMS at TAEnablement@bms.com with the Job Title and Requisition number.
  • Perform other tasks as required to support QC laboratories and product disposition timelines.

Skills

  • Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
  • Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.
  • Attention to detail and demonstrated organizational skills.
  • Problem-solving ability/mentality, technically adept and logical
  • Demonstrated ability to work independently to complete assignments within defined time constraints.
  • Demonstrated ability to effectively train and assist other less experienced individuals.

Company info

  • You can become part of this exciting journey.
  • Why You Should Apply Around the world, we are passionate about making an impact on the lives of patients with serious diseases.
  • 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.
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This listing is sourced directly from Bristol Myers Squibb's careers page and normalized into a canonical job model.