job description
Join RecruitPedia Pte Ltd, a leading name in medical device manufacturing, as our QC Lab Technician (Chemistry) in the vibrant and growing tech hub of Bali, Indonesia. This is an exceptional opportunity for a detail-oriented chemistry professional to play a critical role in ensuring the quality and safety of cutting-edge medical devices. If you have a passion for precision, a background in chemistry, and a commitment to excellence, we want you on our team!
In this role, you will be responsible for conducting rigorous quality control tests, analyzing chemical compositions, and ensuring compliance with international standards. Youâll work in a state-of-the-art laboratory environment, collaborating with cross-functional teams to uphold the highest quality standards in medical device production. Baliâs dynamic work culture, combined with our companyâs innovative spirit, makes this the perfect place to grow your career while enjoying a balanced lifestyle in one of the worldâs most beautiful locations.
At RecruitPedia, we value integrity, innovation, and teamwork. We offer competitive compensation, professional development opportunities, and a supportive work environment where your contributions are recognized and rewarded. If youâre ready to take the next step in your career and make a meaningful impact in the medical device industry, apply today!
Responsibility
- Perform chemical and physical testing on raw materials, in-process samples, and finished medical devices to ensure compliance with specifications and regulatory standards.
- Operate and maintain laboratory equipment, such as HPLC, GC, FTIR, and UV-Vis spectrophotometers, ensuring accurate and reliable test results.
- Document and analyze test data, prepare detailed reports, and present findings to the quality assurance team and management.
- Assist in the development and validation of new testing methods and procedures to improve efficiency and accuracy in quality control processes.
- Ensure compliance with Good Manufacturing Practices (GMP), ISO 13485, and other relevant regulatory requirements for medical devices.
- Collaborate with production, R&D, and regulatory teams to investigate and resolve quality issues, implementing corrective and preventive actions (CAPA).
- Maintain a clean, organized, and safe laboratory environment, adhering to all safety protocols and procedures.
- Stay updated on industry trends, advancements in testing methodologies, and changes in regulatory standards to ensure continuous improvement.
Qualifications
- Bachelorâs degree in Chemistry, Chemical Engineering, Biochemistry, or a related field from an accredited institution.
- Minimum of 2 years of experience in a quality control laboratory, preferably in the medical device, pharmaceutical, or biotechnology industry.
- Hands-on experience with laboratory equipment and techniques, such as HPLC, GC, FTIR, UV-Vis spectroscopy, and wet chemistry methods.
- Strong understanding of GMP, ISO 13485, and other regulatory standards applicable to medical devices.
- Proficiency in data analysis and reporting using software such as LIMS, Excel, or Minitab.
- Excellent attention to detail, analytical skills, and ability to interpret complex technical data.
- Strong communication skills, both written and verbal, with the ability to present findings clearly to cross-functional teams.
- Ability to work independently, manage multiple tasks, and meet deadlines in a fast-paced environment.
- Certification in Quality Control or Regulatory Affairs (e.g., ASQ CQT, RAC) is a plus.