job description
Join Lifework Staffing Services as a Junior Validation Engineer and be part of a dynamic, fast-growing team that is redefining trust and excellence in the Healthcare & Medical industry. This is a unique opportunity for fresh graduates or early-career professionals to develop foundational skills in validation processes, ensuring compliance, quality, and reliability in cutting-edge medical and healthcare solutions.
Based in the vibrant and culturally rich region of Bali (Denpasar, Badung), youâll collaborate with cross-functional teams to deliver high-impact projects that uphold the highest standards of safety and efficiency. Whether youâre passionate about medical devices, pharmaceuticals, or biotechnology, this role offers a structured pathway to grow your expertise in a supportive and innovative environment.
At Lifework Staffing Services, we believe in winning together as one. If youâre eager to contribute to meaningful work while building a rewarding career, weâd love to hear from you.
Responsibility
- Assist in the development, execution, and documentation of validation protocols for medical devices, equipment, or processes in compliance with industry standards (e.g., ISO 13485, FDA 21 CFR Part 11).
- Support the preparation of validation master plans, risk assessments, and test reports to ensure regulatory compliance.
- Collaborate with engineering, quality assurance, and production teams to identify validation requirements and implement solutions.
- Conduct routine inspections and calibration checks to maintain equipment and system integrity.
- Analyze validation data and generate clear, concise reports for internal and external stakeholders.
- Participate in audits (internal/external) and assist in addressing non-conformities or CAPA (Corrective and Preventive Actions).
- Stay updated on industry regulations, best practices, and emerging technologies in validation engineering.
- Contribute to continuous improvement initiatives to enhance validation efficiency and accuracy.
Qualifications
- Bachelorâs degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Pharmacy, or a related field. Fresh graduates are encouraged to apply.
- Basic understanding of validation principles, GMP (Good Manufacturing Practices), or quality systems is a plus.
- Strong analytical, problem-solving, and attention-to-detail skills.
- Proficiency in Microsoft Office (Excel, Word) and familiarity with data analysis tools.
- Excellent written and verbal communication skills in English.
- Ability to work independently and collaboratively in a fast-paced environment.
- Willingness to learn and adapt to new technologies and methodologies.
- Prior internship or project experience in validation, quality control, or a related field is advantageous.