Senior Project Engineer – GMP Pharma Manufacturing

PCI TRGR Penn Pharmaceutical Services Ltd; Bedford (NH); On-site; USD 110,000 - 140,000; Full time

Job summary

PCI Pharma Services is seeking a Project Engineer III to lead complex engineering projects in Bedford, NH. You will collaborate with R&D, manufacturing, QA, and regulatory affairs to ensure successful project execution and compliance with GMP standards.

The role requires 7+ years in GMP/regulatory settings and a solid engineering foundation, with PMP being a plus. This on-site position emphasizes safety, project planning, and cross-department collaboration within a dynamic biopharma environment.

Qualifications

• 7+ years’ experience in GMP/regulated environments.
• Proven project management experience in pharma/biotech.
• Strong understanding of engineering principles applied to manufacturing.

Responsibilities

• Lead and manage complex engineering projects from initiation to completion.
• Develop and implement project management strategies aligned with goals.
• Collaborate with cross-functional teams to ensure project success.
• Evaluate and optimize processes to enhance efficiency.
• Provide technical leadership to project teams.
• Interface with clients and external partners to meet requirements.
• Ensure a safe workplace for contractors and PCI employees.

Skills

GMP/ISO/FDA experience

Project management

Engineering principles

Education

Bachelor's degree in Engineering or related field

Job description

PCI Pharma Services is seeking a Project Engineer III to lead complex engineering projects in Bedford, NH. You will collaborate with R&D, manufacturing, QA, and regulatory affairs to ensure successful project execution and compliance with GMP standards.

The role requires 7+ years in GMP/regulatory settings and a solid engineering foundation, with PMP being a plus. This on-site position emphasizes safety, project planning, and cross-department collaboration within a dynamic biopharma environment.