2,097 Quality Control Specialists jobs in Indonesia

Job Requirements

-Associate degree or above

-More than 1 year as QC Specialist/Staff

-Understand quality system management

-Familiar with the production and quality control processes and basic requirements for medical device products

-Familiar with product production and quality control processes

-Have good organizational coordination, logical thinking, external communication skills, and execution ability.

-Proficient in using office software and data analysis.

• Fluent in English, with Chinese proficiency preferred.

Responsibilities:

• Coaching and monitoring Dept (Collection/CS/Telemarketing)
• Conduct training and being a trainer
• Prepare the material for training based on needs
• Develop agent, do observation & analysis based on training result
• Bring good impact and positive vibes after coaching and training
• Other tasks as assigned

Requirements:

• Willing to work six days in a week (6+1)
• Minimum Diploma degree in any field
• Have experience as QC/QA in Collection,CS,Telemarketing minimum 1 year
• Independent, initiative, and positive
• Good communication & negotiation
• Can work individual and as a team

We are seeking a detail-oriented and analytical Quality Control (QC) Specialist with at least 3 years of experience in the Fintech industry. The ideal candidate will be responsible for ensuring the accuracy, reliability, and compliance of operational processes, data records, and customer transactions. You will work closely with cross-functional teams including Risk, Compliance, Product, and Customer Service to uphold high standards and minimize operational errors.

Key Responsibilities:

• Monitor and review operational workflows, customer transactions, and internal records to ensure accuracy and compliance with company policies and regulatory standards.
• Conduct regular quality checks on documentation, data entries, and customer onboarding processes.
• Collaborate with Risk and Compliance teams to identify potential gaps or process deviations and recommend corrective actions.
• Prepare and maintain detailed QC reports, error logs, and process audits for internal review and external audit requirements.
• Implement quality control best practices and continuously improve QC procedures and checklists.
• Train or support operational teams on quality standards and ensure adherence to updated SOPs.
• Support system testing and UAT (User Acceptance Testing) to ensure data and logic integrity.
• Stay updated with the latest industry regulations (e.g., OJK, ISO, AML/KYC guidelines) relevant to operational controls.

Requirements:

• Minimum 3 years of experience in a Quality Control, Operational Risk, or Compliance role within the Fintech or Financial Services industry.
• Strong understanding of fintech operational flows such as loan processing, e-wallet transactions, customer verification (KYC), or payment gateways.
• Excellent attention to detail and analytical thinking skills.
• Familiarity with QC tools, data validation methods, or workflow audit systems.
• Proficient in Microsoft Excel or Google Sheets; experience with CRM or ticketing tools is a plus.
• Strong communication skills and ability to work cross-functionally.
• Able to work in a fast-paced and regulated environment.

• Develop, implement, and maintain comprehensive quality control plans and procedures for various manufacturing lines.
• Lead and mentor a team of quality control inspectors, providing training and performance feedback.
• Conduct in-depth inspections and testing of raw materials, in-process components, and finished products using appropriate tools and methodologies.
• Analyze quality data, identify trends, and develop action plans to address deviations and non-conformities.
• Collaborate closely with production, engineering, and R&D teams to resolve quality issues and implement corrective and preventive actions (CAPA).
• Ensure compliance with relevant industry standards, certifications (e.g., ISO 9001), and customer specifications.
• Maintain accurate and organized records of all quality control activities, test results, and inspection reports.
• Conduct internal audits to assess the effectiveness of the quality management system and identify areas for improvement.
• Stay abreast of the latest quality control techniques, technologies, and regulatory requirements.
• Contribute to the development and continuous improvement of manufacturing processes to enhance product quality and efficiency.

• Bachelor's degree in Engineering (Mechanical, Industrial, or related), Science, or a relevant technical field.
• Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
• Proven experience with quality management systems (QMS), such as ISO 9001.
• Strong understanding of statistical process control (SPC) and other quality analysis tools.
• Excellent analytical, problem-solving, and decision-making skills.
• Proficiency in using inspection equipment and measurement tools.
• Demonstrated leadership abilities, with experience supervising or mentoring junior staff.
• Exceptional attention to detail and a commitment to accuracy.
• Strong written and verbal communication skills, with the ability to effectively communicate technical information.
• Proficiency in data analysis software and Microsoft Office Suite.
• Ability to work independently and manage workload effectively in a remote setting.

• Perform analytical testing on raw materials, in-process samples, and finished pharmaceutical products according to established methods and SOPs.
• Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.
• Prepare reagents, solutions, and standards required for testing.
• Document all testing activities, results, and deviations accurately and thoroughly in compliance with GMP guidelines.
• Review and analyze test data, identifying any out-of-specification (OOS) results and participating in investigations.
• Ensure laboratory equipment is calibrated, qualified, and maintained in good working order.
• Participate in method validation and transfer activities.
• Contribute to the continuous improvement of quality control processes and procedures.
• Maintain a safe and organized laboratory environment, adhering to all safety regulations.
• Collaborate with other departments, including Production, Quality Assurance, and Research & Development.
• Stay up-to-date with current industry trends, regulatory requirements (e.g., BPOM, FDA), and scientific advancements.
• Prepare and review quality control documentation, including Certificates of Analysis (CoA).

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 3 years of experience in pharmaceutical quality control or a similar laboratory setting.
• Hands-on experience with common analytical techniques and instrumentation used in pharmaceutical testing (HPLC, GC, KF Titration, etc.).
• Strong knowledge of Good Manufacturing Practices (GMP), pharmacopoeial standards (e.g., USP, EP), and regulatory requirements.
• Excellent attention to detail and accuracy in data recording and analysis.
• Proficiency in using laboratory software and data management systems.
• Strong problem-solving and critical thinking skills.
• Good written and verbal communication skills in Bahasa Indonesia and English.
• Ability to work effectively both independently and as part of a team.
• Familiarity with stability testing programs is a plus.
• Experience with statistical analysis software for quality control is advantageous.

• Implement and oversee quality control procedures on the production line.
• Conduct inspections of incoming materials, in-process components, and finished vehicles.
• Identify and document non-conforming products and implement corrective actions.
• Utilize various measurement and testing equipment to verify product specifications.
• Analyze quality data to identify trends and root causes of defects.
• Collaborate with production teams to resolve quality issues promptly.
• Ensure adherence to automotive industry quality standards (e.g., IATF 16949).
• Contribute to the development and improvement of quality control processes.
• Maintain accurate quality records and documentation.
• Participate in internal and external quality audits.
• Promote a quality-focused culture throughout the manufacturing plant.
• Train production staff on quality standards and inspection techniques.

• Diploma or Bachelor's degree in Mechanical Engineering, Automotive Engineering, or a related technical field.
• Minimum of 3-5 years of experience in quality control within the automotive industry.
• Strong knowledge of quality management principles and tools (e.g., Six Sigma, SPC).
• Proficiency in using inspection tools and equipment.
• Excellent attention to detail and analytical skills.
• Ability to read and interpret technical drawings and specifications.
• Good communication and teamwork skills.
• Understanding of lean manufacturing principles is advantageous.
• Experience with automotive quality standards is essential.
• Must be able to work full-time on-site in Tasikmalaya.

• Developing and validating analytical methods for raw materials, in-process samples, and finished products.
• Performing comprehensive quality control testing using various laboratory techniques (e.g., HPLC, GC, spectroscopy).
• Reviewing and interpreting test results, ensuring compliance with specifications and regulatory standards.
• Investigating out-of-specification (OOS) results and implementing corrective and preventive actions (CAPAs).
• Contributing to the development and implementation of quality assurance programs and SOPs.
• Participating in internal and external audits, and ensuring readiness for regulatory inspections.
• Monitoring and reporting on quality metrics and key performance indicators.
• Providing training and guidance to junior quality control personnel.
• Staying updated on pharmaceutical regulations and industry best practices.
• Collaborating with cross-functional teams to resolve quality-related issues and ensure product release.

• Develop, implement, and manage quality control standards and procedures.
• Conduct regular inspections and audits of products and processes.
• Analyze quality data, identify trends, and report on key performance indicators.
• Perform root cause analysis for product defects and non-conformities.
• Implement and track corrective and preventive actions (CAPA).
• Ensure compliance with relevant industry standards and regulations (e.g., ISO).
• Collaborate with R&D, production, and operations teams to address quality issues.
• Train and mentor junior quality assurance personnel.
• Maintain accurate quality documentation and records.
• Contribute to the continuous improvement of the quality management system.

• Bachelor's degree in Engineering, Chemistry, Biology, or a related scientific field.
• Minimum of 6 years of experience in quality control or quality assurance, preferably in the manufacturing or chemical industry.
• In-depth knowledge of Quality Management Systems (QMS), such as ISO 9001.
• Proficiency in statistical process control (SPC) and data analysis tools.
• Experience with root cause analysis methodologies (e.g., 5 Whys, Ishikawa diagrams).
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong written and verbal communication skills.
• Ability to work independently and manage time effectively in a remote setting.
• Relevant certifications (e.g., CQE, CQA) are highly desirable.