Capital Project Manager - Biotech Capital Projects (Hybrid)

Bristol Myers Squibb

Harvard (MA)

On-site

USD 110,000 - 134,000

Full time

6 days ago
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Benefits offered by this job

Health Coverage
Wellbeing Support Programs
Financial Well-being and Protection
Paid Time Off

Job summary

Bristol Myers Squibb is seeking a Capital Project Manager for the Devens, MA site to lead planning, design, and close-out of capital projects, ensuring budgetary and regulatory compliance. You will coordinate design, cost estimates, schedules, and vendor oversight across functions.

The role requires a BS in engineering and at least 6 years of experience in conceptual development, project management, and manufacturing support in biotech or related industries.

Qualifications

  • Bachelor degree in engineering (mechanical, electrical or chemical preferred).
  • Minimum 6 years in conceptual development, project management, planning and scheduling on capital projects, incl. Biotech or related industry.
  • Knowledge of regulatory requirements, engineering principles, and construction techniques.
  • Demonstrated proficiency communicating and collaborating across levels with customers, vendors and operations staff.
  • Experience in supporting manufacturing operations is desired.

Responsibilities

  • Coordinate project design, cost estimates, schedule, interface with client on capital projects.
  • Manage capital project implementation including oversight of selected vendors.
  • Ensure customers, peers, and support groups understand scope and deliverables for assigned capital projects.
  • Support Lead Project Manager on capital projects.

Skills

Engineering degree
Capital project management
Regulatory knowledge
Communication
Manufacturing operations
Leadership
Team collaboration
Accountability

Education

Bachelor of Science in engineering

Job description

Bristol Myers Squibb is seeking a Capital Project Manager for the Devens, MA site to lead planning, design, and close-out of capital projects, ensuring budgetary and regulatory compliance. You will coordinate design, cost estimates, schedules, and vendor oversight across functions.

The role requires a BS in engineering and at least 6 years of experience in conceptual development, project management, and manufacturing support in biotech or related industries.

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