Key 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 methodologies systems practices which meets BSC, customer and regulatory requirements.
Create, and revise, departmental procedures.
Acts 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.
Responsible for reviewing and developing validation protocols and reports. Support other functional areas during the validation activities
Interface with other engineering departments within the company, customers, and suppliers on quality related issues.
Conversant with validation techniques and associated regulatory requirements

Requirements

Minimum Degree in Engineering or Science
1-3 years of experience in Operations Quality. Prior experience in the medical device industry is preferred.
Required skills: Resolves issues using standard problem-solving tools and a strong 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 in product transfer will be added advantage.