Junior Quality Assurance (Automation​/Katalon

Our client is seeking a meticulous and experienced Quality Assurance Specialist to enhance their quality systems in Bekasi . This role is essential for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout their lifecycle. You will be involved in developing, implementing, and maintaining quality assurance programs, conducting audits, and driving continuous improvement initiatives. This position offers a significant opportunity to impact product quality and patient safety within a leading pharmaceutical manufacturing facility in West Java .

About the Role

Our client is seeking a diligent and experienced Quality Assurance Specialist to enhance their quality systems in Bekasi . This role is essential for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout their lifecycle. You will be involved in developing, implementing, and maintaining quality assurance programs, conducting audits, and driving continuous improvement initiatives. This position offers a significant opportunity to impact product quality and patient safety within a leading pharmaceutical manufacturing facility in West Java .

• Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with cGMP and other relevant regulations.
• Conduct internal audits of manufacturing processes, documentation, and facilities to ensure compliance.
• Review and approve batch records, specifications, validation protocols, and other quality-related documents.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPA).
• Participate in external regulatory inspections and customer audits, acting as a point of contact for QA matters.
• Provide quality assurance training to relevant personnel within the organization.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 3 years of experience in Quality Assurance within the pharmaceutical industry.
• Strong knowledge of cGMP (current Good Manufacturing Practices) , regulatory guidelines (e.g., BPOM), and quality systems.
• Experience with audits, deviation investigations, CAPA management, and change control processes.
• Excellent analytical, problem-solving, and documentation skills.
• Ability to work effectively both independently and as part of a cross-functional team in a hybrid setting.

• Competitive annual salary and performance incentives.
• Hybrid work schedule offering a balance between office and remote work.
• Comprehensive medical, dental, and vision insurance coverage.
• Paid time off, including vacation and sick leave.
• Opportunities for professional development and career growth in quality assurance.