job description
Join PT. ELVINCO MED TECH, a leader in medical device manufacturing, as a Quality Control Specialist in the vibrant region of Badung, Bali. This role is perfect for detail-oriented professionals passionate about ensuring the highest standards of product quality, safety, and compliance in a dynamic, fast-paced environment.
As part of our team, you will play a critical role in maintaining GMP (Good Manufacturing Practices) and SOP (Standard Operating Procedures) while contributing to the production of life-saving medical devices. Your work will directly impact patient safety and product reliability, making this a highly rewarding opportunity for those committed to excellence in healthcare manufacturing.
We offer a competitive salary, a collaborative work culture, and the chance to grow within a company that values precision, innovation, and integrity. If you thrive in structured environments and are ready to take on shift-based responsibilities, we invite you to apply and help us uphold the highest quality standards in the industry.
Responsibility
- Operate and assemble medical devices strictly in accordance with SOP and GMP guidelines to ensure compliance with industry standards.
- Conduct thorough quality inspections on raw materials, in-process products, and finished goods to identify defects or deviations.
- Maintain accurate and detailed quality control records, documentation, and reports for traceability and audits.
- Ensure workplace safety, cleanliness, and hygiene in compliance with company and regulatory requirements.
- Collaborate with production teams to troubleshoot quality issues and implement corrective actions.
- Perform calibration and maintenance of testing equipment to ensure accuracy and reliability.
- Participate in continuous improvement initiatives to enhance product quality and process efficiency.
- Adhere to shift schedules and meet production deadlines without compromising quality standards.
Qualifications
- Bachelor’s degree in Engineering, Pharmaceutical Sciences, or a related field (fresh graduates are welcome).
- Strong attention to detail and a commitment to maintaining high-quality standards.
- Basic understanding of GMP, ISO 13485, or other medical device quality standards is a plus.
- Ability to work in shift-based environments (including nights, weekends, or holidays as required).
- Excellent documentation and record-keeping skills with a focus on accuracy.
- Non-smoker (company policy requirement).
- Proficient in Microsoft Office (Excel, Word) for reporting and data analysis.
- Strong teamwork and communication skills to collaborate effectively with cross-functional teams.