Night-Shift Quality Engineer Onsite – ISO/FDA Focus

Abbott; Scarborough (ME); Presencial; USD 65 000 - 90 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical plan

Dental plan

Vision plan

Health Savings Account

Flexible Spending Accounts

Long term disability

401(k)

Resumo da oferta

Abbott is seeking an Engineer, Quality for a 3‑month onsite engagement in Scarborough, Maine. You will support production on the floor, resolve quality issues, and ensure proper DHR documentation while upholding ISO, FDA, and regulatory standards.

The role requires a technical degree and strong writing and communication skills, with experience in cGMP environments and quality systems. Onsite shift runs 10PM–6:30AM.

Qualificações

• Bachelor's Degree in Engineering, Chemistry, Biotechnology, Life Science or other technical field or equivalent.
• Experience applying FDA/cGMP/QSR and ISO quality system requirements.

Responsabilidades

• Support production with resolution of quality issues in accordance with established procedures.
• Support production on the manufacturing floor, ensuring adherence to procedures and proper DHR documentation.
• Assist line clearances, reworks, and inspections as required.
• Contribute to the development and effectiveness of the Quality Management System per ISO, FDA, and other regulatory agencies.
• Maintain professional behavior and align with company policies and practices.
• Understand quality consequences of job performance and potential device defects across design, verification/validation, manufacturing and testing.
• Perform other duties as assigned to meet business needs.

Conhecimentos

Technical writing

Communication

Quality management

FDA compliance

cGMPs/QSR

Formação académica

Bachelor's degree

Engineering background

Ferramentas

Database software

Internet software

Inventory software

Spreadsheet software

Word processing software

Descrição da oferta de emprego

Abbott is seeking an Engineer, Quality for a 3‑month onsite engagement in Scarborough, Maine. You will support production on the floor, resolve quality issues, and ensure proper DHR documentation while upholding ISO, FDA, and regulatory standards.

The role requires a technical degree and strong writing and communication skills, with experience in cGMP environments and quality systems. Onsite shift runs 10PM–6:30AM.