job description
Join ScienTec Consulting, a leading global medical device manufacturer, as a Quality Technician - Biomedical. This is a unique opportunity to contribute to the production of life-saving medical devices while ensuring the highest standards of quality and compliance. Based in the vibrant regions of Bali, you will play a crucial role in maintaining the integrity and safety of biomedical products that impact lives worldwide.
As a Quality Technician, you will work in a state-of-the-art manufacturing environment, collaborating with cross-functional teams to uphold rigorous quality control protocols. Your meticulous attention to detail and commitment to excellence will directly support our mission of delivering reliable and innovative medical solutions.
If you are passionate about quality assurance and eager to advance your career in the biomedical field, we invite you to apply and become part of our dynamic team.
Responsibility
- Perform thorough inspections of biomedical devices to ensure compliance with industry standards and regulatory requirements.
- Conduct routine quality control tests and document results accurately in compliance with company protocols.
- Identify and report any deviations or defects in products, initiating corrective actions as necessary.
- Collaborate with production teams to implement quality improvement initiatives and optimize manufacturing processes.
- Maintain and calibrate inspection equipment to ensure precision and reliability in testing procedures.
- Assist in the development and revision of quality control procedures and work instructions.
- Participate in internal and external audits to ensure adherence to quality management systems.
- Support continuous improvement projects to enhance product quality and operational efficiency.
Qualifications
- Diploma or degree in Biomedical Engineering, Quality Assurance, or a related field.
- Minimum of 2 years of experience in quality control or inspection within the medical device or pharmaceutical industry.
- Strong knowledge of quality standards such as ISO 13485, FDA regulations, and GMP guidelines.
- Proficient in using inspection tools and equipment, with a keen eye for detail.
- Excellent documentation skills and familiarity with quality management software.
- Ability to work effectively in a team-oriented environment and communicate technical information clearly.
- Strong problem-solving skills and a proactive approach to identifying and resolving quality issues.
- Certification in quality control or biomedical technologies is a plus.