Quality Engineer

Responsibilities

Identify and implement effective process control systems to support the development, qualification, and on‑going manufacturing of products to meet or exceed internal and external requirements

Ensure quality engineering methodology systems practices meet BSC, customer and regulatory requirements.

Create and revise departmental procedures.

Act as an effective leader or team member in supporting quality disciplines, decisions, and practices.

Apply sound, systematic problem‑solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.

Assure in the development and execution of streamlined business systems which effectively identify and resolve quality issues.

Develop testing and inspection methodologies and documentation for new and existing products. Generate test protocols/reports and execute qualification and validation testing.

Review and develop validation protocols and reports. Support other functional areas during validation activities.

Interface with other engineering departments, customers, and suppliers on quality‑related issues.

Possess knowledge of validation techniques and associated regulatory requirements.

Qualifications

Minimum degree in engineering or science.

At least 5 years of experience in operations quality; experience in the medical device industry preferred.

Strong problem‑solving skills using standard tools and a solid understanding of quality operations fundamentals, including product risk assessment and data analysis to identify root causes and drive solutions. Communicates findings clearly and effectively. Process validation experience essential.

Experience in product transfer will be an added advantage.

Requisition ID: 604223 Job Segment Medical Device Engineer, Quality Engineer, Medical Device, Inspector, Manufacturing Engineer, Engineering, Healthcare, Quality

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