Facilities Operations Manager - Biopharma

Syngene International

Baltimore (MD)

On-site

USD 120,000 - 180,000

Full time

16 hours ago
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Job summary

Syngene International is seeking a Manager of Facilities in Baltimore to lead the Facility Services group, ensuring day-to-day operations and regulatory compliance across maintenance, metrology, and planning functions.

The role requires a seasoned leader with biopharma experience, strong budgeting and project management skills, and a track record of safety and quality discipline within cGMP environments.

Qualifications

  • Bachelor’s degree in Business, Science, Engineering, or related field preferred.
  • 10+ years in a biopharmaceutical environment with at least 7+ years in a leadership role.
  • Experience with budget preparation and scheduling.
  • Prior cGMP experience is required.
  • Proficiency in Microsoft Project, Word, and Excel.

Responsibilities

  • Oversee day-to-day operations of the Facility Services group.
  • Lead General Maintenance, Manufacturing Support, Metrology, and Facility Resource Planning.
  • Ensure facilities and systems meet cGMP and regulatory standards.
  • Own Quality Systems within Facilities (Deviations, CAPAs, SOP revisions, Change Control).
  • Manage safety policies and departmental documentation in SAP.
  • Plan goals, allocate resources, and manage budgets.
  • Coordinate cross-functional shutdowns for preventive maintenance.
  • Act as site lead during internal and external audits.
  • Support capital projects as SME for plant equipment and systems.
  • Foster staff development through coaching and training.

Skills

Leadership
Communication
Project management
Budgeting
Maintenance knowledge

Education

Bachelor’s degree in Business, Science, Engineering, or related field
10+ years in biopharma with 7+ years in leadership

Tools

SAP
Microsoft Project
Excel
Word

Job description

Syngene International is seeking a Manager of Facilities in Baltimore to lead the Facility Services group, ensuring day-to-day operations and regulatory compliance across maintenance, metrology, and planning functions.

The role requires a seasoned leader with biopharma experience, strong budgeting and project management skills, and a track record of safety and quality discipline within cGMP environments.

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Equal Opportunity Employer