Senior Director, Biologics Manufacturing Operations

Bristol Myers Squibb

Harvard (MA)

On-site

USD 180,000 - 280,000

Full time

3 days ago
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Job summary

Bristol Myers Squibb seeks a senior manufacturing leader to direct Upstream/Downstream operations, drive production targets, and ensure cGMP compliance for biologics manufacturing. You will manage a large, diverse team and align schedules with supply chain needs while advancing process improvement and capital efficiency.

Responsibilities include safety leadership, cross-functional collaboration, and delivering on New Product Introductions in a fast-paced biotech environment.

Qualifications

  • Knowledge of SOPs, cGMPs and know-how to work within a regulatory environment.
  • Extensive knowledge of pharmaceutical and biopharm manufacturing processes and tech transfer.
  • Experience managing large teams (>30 people).
  • Aptitude for engineering principles and manufacturing automation systems.
  • Ability to influence in a matrixed environment.
  • Proven managerial experience in selection, motivation and retention of staff.

Responsibilities

  • Directs all activities in Upstream or Downstream Operations.
  • Allocates departmental resources to deliver production targets and manage turnover/training.
  • Accountable for multiproduct operations including New Product Introductions.
  • Owns detailed work schedules aligned with supply chain demand and site programs.
  • Drives safety leadership and ensures CAPA closure.
  • Ensures cGMP performance and regulatory compliance.
  • Maintains audit readiness for facility and SME.

Skills

Leadership
Regulatory compliance
Project management
Manufacturing operations
cGMP knowledge
Team building
Process optimization
Communication

Education

B.S. in science/engineering
M.S. or related field preferred

Tools

Process automation software
SPC
Quality systems (LIMS/MES)

Job description

Bristol Myers Squibb seeks a senior manufacturing leader to direct Upstream/Downstream operations, drive production targets, and ensure cGMP compliance for biologics manufacturing. You will manage a large, diverse team and align schedules with supply chain needs while advancing process improvement and capital efficiency.

Responsibilities include safety leadership, cross-functional collaboration, and delivering on New Product Introductions in a fast-paced biotech environment.

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