Biopharma Equipment Engineer - Process Systems

Regeneron Pharmaceuticals; City of Troy (NY); Presencial; USD 88 000 - 169 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Total rewards package

Healthcare benefits

On-site role in Troy

Resumo da oferta

Regeneron Pharmaceuticals in Troy, New York, is seeking an Equipment Engineer to specify and commission small process equipment and components for biopharmaceutical manufacturing, and to evaluate functional equivalence to existing systems. The position supports design reviews, site acceptance, and installation, with emphasis on cGMP standards.

The role involves writing test plans to demonstrate equipment suitability, assisting QA Validation, and developing standard equipment specifications,

Qualificações

• BS/BA in engineering required; chemical/biochemical/mechanical preferred.
• 5+ years for Senior level; 8+ for Principal.
• Experience with biopharmaceutical process equipment desirable.

Responsabilidades

• Specify cGMP process equipment, components, and spare parts.
• Evaluate equipment for Functional Equivalence to existing equipment.
• Assist in design review, site acceptance, and installation of equipment.
• Write and execute test plans demonstrating equipment suitability.
• Support QA Validation by preparing design documents and assisting in protocol execution.
• Author, review, and revise Standard Equipment Specifications.
• Implement corrective/preventative actions for existing equipment.
• Prepare engineering evaluations and test plans for change control.
• Support large capital projects in spare parts capacity.

Conhecimentos

CAD software

Communication skills

Formação académica

B.S./B.A. in engineering

Descrição da oferta de emprego

Regeneron Pharmaceuticals in Troy, New York, is seeking an Equipment Engineer to specify and commission small process equipment and components for biopharmaceutical manufacturing, and to evaluate functional equivalence to existing systems. The position supports design reviews, site acceptance, and installation, with emphasis on cGMP standards.

The role involves writing test plans to demonstrate equipment suitability, assisting QA Validation, and developing standard equipment specifications,