Senior Bioprocess Engineer - GMP Manufacturing & Validation

GSK; United States; On-site; USD 90,000 - 120,000; Full time

Job summary

GSK is seeking a process engineer to advance manufacturing of drug substances and vaccines. You will develop and optimize processes to produce medicines safely and efficiently, collaborating with cross-functional partners who value science, quality and continuous improvement.

We value engineers who are curious, practical problem solvers and strong communicators. This role provides opportunities to lead meaningful projects and contribute to delivering high-quality medicines to patients.

Qualifications

• Bachelor's degree in engineering or science is required.
• Minimum 5+ years of process engineering experience in pharma or medical device manufacturing.
• Experience with GMP, vaccine or pharma formulation and filling facilities.

Responsibilities

• Lead design, procurement, installation, validation and support of bioprocess equipment and facilities.
• Coordinate cross-functional teams; develop SOPs and device standards; improve throughput.
• Interface with outside engineering firms on design issues and compliance.
• Manage vendors and contractors to ensure cGMP compliance and project success.
• Stay current with tech developments in vaccine/formulation and equipment design.

Skills

Process engineering

GMP experience

Education

Bachelor's degree in engineering

Job description

GSK is seeking a process engineer to advance manufacturing of drug substances and vaccines. You will develop and optimize processes to produce medicines safely and efficiently, collaborating with cross-functional partners who value science, quality and continuous improvement.

We value engineers who are curious, practical problem solvers and strong communicators. This role provides opportunities to lead meaningful projects and contribute to delivering high-quality medicines to patients.