job description
Join New Myrex Laboratories Inc. as a Quality Assurance Supervisor in the vibrant region of Badung, Bali. This is a unique opportunity to lead quality control initiatives in a dynamic manufacturing and logistics environment, ensuring compliance with industry standards and driving operational excellence.
In this pivotal role, you will oversee quality assurance processes, implement best practices, and collaborate with cross-functional teams to maintain the highest standards of product integrity. Your expertise will directly contribute to enhancing efficiency, reducing defects, and fostering a culture of continuous improvement.
Based in one of Baliâs most strategic locationsâclose to Canggu, Ubud, Denpasar, or Jimbaranâyouâll enjoy a professional setting with opportunities for growth in a globally connected industry. If you are a detail-oriented leader with a passion for quality and process optimization, we invite you to apply and take the next step in your career.
Responsibility
- Develop, implement, and maintain quality assurance policies, procedures, and standards in accordance with industry regulations (e.g., ISO, GMP).
- Supervise and train QA staff to ensure adherence to protocols and consistent product quality.
- Conduct regular audits, inspections, and testing of raw materials, in-process products, and finished goods.
- Investigate and resolve quality-related issues, including non-conformances, deviations, and customer complaints.
- Collaborate with production, R&D, and supply chain teams to identify and mitigate quality risks.
- Prepare and present quality reports, metrics, and improvement recommendations to senior management.
- Ensure compliance with local and international quality standards, including documentation and record-keeping.
- Drive continuous improvement initiatives (e.g., Lean, Six Sigma) to enhance efficiency and reduce waste.
Qualifications
- Bachelorâs degree in Pharmacy, Chemistry, Chemical Engineering, or related field; Masterâs degree is a plus.
- Minimum 5 years of experience in Quality Assurance within manufacturing, pharmaceuticals, or logistics, with at least 2 years in a supervisory role.
- In-depth knowledge of GMP, ISO 9001, HACCP, or other relevant quality standards.
- Strong analytical and problem-solving skills with experience in root cause analysis (RCA) and CAPA.
- Proficient in quality management systems (QMS) and data analysis tools (e.g., Minitab, Excel).
- Excellent leadership, communication, and interpersonal skills to manage teams and stakeholder relationships.
- Familiarity with regulatory requirements for local and international markets (e.g., FDA, EU, ASEAN).
- Ability to work in a fast-paced environment with a commitment to deadlines and precision.