Senior Process Engineering Manager – Biotech & Gene Therapy

Genezen; Lexington (MA); On-site; USD 130,000 - 170,000; Full time

Benefits offered by this job

Paid vacation days

401(k) plan with company match

Healthcare plans

FSA and HSA programs

Life and disability insurance

Job summary

GENEZEN in Lexington, MA is seeking a Manager/Sr. Manager of Process Engineering to lead the department, drive equipment upgrades, and oversee process improvements for GMP viral vector manufacturing. You will represent Engineering in client meetings and guide project execution from design through turnover.

You will manage staff, align goals with corporate objectives, and ensure on-time delivery while maintaining quality and safety standards in a fast-growth biopharma setting.

Qualifications

• B.S. in Chemical, Biomolecular, or Biomedical Engineering.
• Essential 8+ years of relevant experience including 3 years of management experience.
• Experience with single-use process equipment and process validation is preferred.

Responsibilities

• Represent department in client and cross-functional meetings as key stakeholder.
• Drive equipment, control system, and facility improvement projects within schedule and budget.
• Provide technical input for product tech transfers and deviations resolution.
• Mentor engineering staff and set team goals and performance reviews.

Skills

Leadership

Project management

Process engineering

Bioprocess

Communication

Team mentorship

Problem solving

Regulatory compliance

Multi-tasking

Technical troubleshooting

Education

B.S. in Chemical, Biomolecular, or Biomedical Engineering

Tools

Bioreactors

Chromatography skids

UF/DF systems

Fill-finish equipment

WFI and Pure Steam utilities

Compressed gas systems

Microsoft Office

Job description

GENEZEN in Lexington, MA is seeking a Manager/Sr. Manager of Process Engineering to lead the department, drive equipment upgrades, and oversee process improvements for GMP viral vector manufacturing. You will represent Engineering in client meetings and guide project execution from design through turnover.

You will manage staff, align goals with corporate objectives, and ensure on-time delivery while maintaining quality and safety standards in a fast-growth biopharma setting.