Quality Control Inspector

Selamat Datang di Situs Lowongan Kerja Indonesia Terbaru 2026 dan Saat ini kami ingin memberitahukan Info Terbaru Mengenai Informasi Loker dari Perusahaan Pt Surya Sealindo Teknologi dengan posisi Quality Control Inspector. Untuk selengkapnya silahkan baca deskripsi lowongan kerja di bawah ini dengan seksama dan teliti, beserta persyaratan minimal lowongan kerja di yang telah tertera dan dijelaskan di bawah ini.

Pt Surya Sealindo Teknologi melalui program rekrutmennya saat ini sedang membuka lowongan kerja untuk posisi Quality Control Inspector di Jawa yang bertujuan untuk meningkatkan kinerja operasional di dalam maupun luar kantor Pt Surya Sealindo Teknologi. Perusahaan Tersebut sedang mencari calon tenaga kerja yang siap diterjunkan ke setiap divisi bagian perusahaan yang sesuai dengan posisi, kemampuan dan keahlian para pencari kerja tersebut. Berikut ini adalah detail lengkap persyaratan untuk posisi Quality Control Inspector di Jawa Perusahaan Pt Surya Sealindo Teknologi:

Senior Quality Control Inspector – Manufacturing

Our client, a leading manufacturer of high‑precision components, is seeking a diligent and detail‑oriented Senior Quality Control Inspector. The role is critical to ensuring that all products meet stringent quality standards before leaving the facility.

• Conduct thorough inspections of incoming materials, in‑process products, and finished goods.
• Utilize a range of measuring instruments (e.g., calipers, micrometers, CMMs) and testing equipment.
• Interpret engineering drawings, blueprints, and specifications to verify product conformance.
• Identify and document quality issues, defects, and non‑conformances accurately.
• Collaborate with production, engineering, and quality assurance teams to resolve quality problems.
• Implement and monitor statistical process control (SPC) techniques.
• Maintain accurate and organized quality control records and documentation.
• Calibrate and maintain inspection and testing equipment.
• Participate in quality audits and continuous improvement initiatives.
• Ensure adherence to all safety regulations and company quality policies.
• Train junior inspectors on inspection procedures and techniques.
• Provide feedback to suppliers regarding material quality.

• High school diploma or equivalent; technical certification in Quality Assurance or a related field is a plus.
• Minimum of 5 years of experience in quality control inspection within a manufacturing environment.
• Proficiency in using various measuring and testing instruments, including Coordinate Measuring Machines (CMMs).
• Strong understanding of quality control principles, methodologies, and standards (e.g., ISO 9001).
• Ability to read and interpret technical drawings, blueprints, and specifications.
• Experience with Statistical Process Control (SPC).
• Excellent attention to detail and accuracy.
• Strong problem‑solving and analytical skills.
• Good communication and teamwork abilities.
• Familiarity with Lean Manufacturing concepts is advantageous.

QA Engineer – Manual & Automation

We are looking for a skilled QA Engineer to ensure the quality and reliability of our systems through comprehensive testing strategies.

• Develop and execute comprehensive test plans, test cases, and test scenarios (functional & non‑functional).
• Perform manual testing across multiple system modules.
• Design, develop, and maintain automated test scripts using tools such as Selenium, Cypress, or Playwright.
• Implement and maintain API automation testing using Postman, REST Assured, or similar tools.
• Execute and manage regression testing to ensure system stability after updates or deployments.
• Participate in System Integration Testing (SIT) and User Acceptance Testing (UAT).
• Identify, document, and track defects using tools like Jira, including clear reproduction steps and severity classification.
• Conduct database validation and ensure data integrity across Oracle, PostgreSQL, and MongoDB.
• Perform performance and load testing to validate system scalability and responsiveness.
• Collaborate with developers, business analysts, and project managers to ensure proper requirement understanding and test coverage.
• Generate test reports, defect metrics, and quality dashboards for stakeholders.
• Continuously improve QA processes, including test automation, CI/CD integration, and shift‑left practices.

• 3–5 years of experience as a QA Engineer (manual & automation).
• Bachelor’s degree in Information Systems, Computer Science, or a related field.
• Strong experience with at least one automation framework (Selenium, Cypress, Playwright, etc.).
• Solid understanding of SQL for database testing (Oracle, PostgreSQL).
• Familiarity with NoSQL databases (MongoDB).
• Experience with CI/CD tools (Jenkins, GitLab CI, or similar).
• Proficiency in bug tracking & test management tools (Jira, TestRail, Zephyr, etc.).
• Understanding of Agile/Scrum methodologies.
• Experience in performance testing tools (JMeter, k6, Gatling) is a plus.
• Background in banking, financial services, or loyalty systems is preferred.
• Strong analytical thinking, problem‑solving, and communication skills.

Senior Pharmaceutical Quality Control Analyst

Our client, a leading pharmaceutical company, is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join their state‑of‑the‑art laboratory.

• Perform a wide range of analytical tests on raw materials, in‑process samples, and finished products using techniques such as HPLC, GC, UV‑Vis, Karl Fischer titration, and dissolution testing.
• Prepare reagents, standard solutions, and samples for testing according to established procedures.
• Operate and maintain laboratory equipment, ensuring calibration and performance verification.
• Accurately record and document all testing procedures, results, and observations in laboratory notebooks and electronic systems.
• Interpret analytical data, identify deviations from specifications, and investigate out‑of‑specification (OOS) results.
• Write and review analytical test methods, standard operating procedures (SOPs), and validation protocols.
• Participate in internal audits and inspections to ensure compliance with cGMP and regulatory requirements.
• Collaborate with R&D, manufacturing, and regulatory affairs departments to resolve quality issues.
• Train junior analysts on laboratory techniques, procedures, and cGMP principles.
• Stay current with pharmacopeial requirements (USP, EP) and industry best practices.
• Contribute to continuous improvement initiatives within the QC laboratory.

• Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, Biology, or a related field.
• Minimum of 5 years of experience in pharmaceutical quality control or analytical chemistry.
• Extensive hands‑on experience with analytical instrumentation commonly used in the pharmaceutical industry (HPLC, GC, etc.).
• Strong understanding of cGMP regulations and quality systems in the pharmaceutical industry.
• Proficiency in data analysis, interpretation, and troubleshooting.
• Excellent documentation skills and attention to detail.
• Strong understanding of pharmacopeial standards.
• Ability to work independently and as part of a team in a laboratory environment.
• Good communication and interpersonal skills.
• Experience with method validation and qualification is a significant advantage.

Aviation Quality Assurance Engineer

• Be well‑versed in the company’s manuals, SOPs, forms, and applicable regulations/legislation.
• Maintain, review, implement, and oversee the Quality Management System (QMS), Safety Management System (SMS), and standardization across the group.
• Assist in planning, conducting, and following up on internal audits.
• Perform quality and safety inspections, prepare findings, and summarize reports.
• Deliver internal quality and safety induction training, toolbox briefings, and other mandatory training programs.
• Provide support during external audits and liaise with relevant authorities and stakeholders.

• Bachelor’s degree in Engineering or a related field.
• Minimum 2 years of experience in the aviation industry.
• Certified or experienced as a Qualified Internal Auditor; Lead Auditor certification is an advantage.
• Hands‑on experience in Safety Management Systems (SMS).
• Strong interpersonal skills, with the ability to collaborate across departments and interact effectively with stakeholders.
• Excellent planning and organizational skills, with the ability to work independently.
• Strong analytical and problem‑solving abilities.
• Detail‑oriented, with a strong focus on quality, safety, and professional ethics.
• Proficiency in IT tools for report preparation and data analysis.
• Good knowledge of ISO 9001, QMS, and other relevant ISO standards.

Senior Quality Assurance Analyst – Pharmaceutical

Our client, a leading pharmaceutical company headquartered in Jakarta, Jakarta, ID, is seeking an experienced Senior Quality Assurance Analyst.

• Develop, validate, and implement quality assurance procedures and protocols for pharmaceutical products.
• Conduct internal audits and inspections of manufacturing processes, facilities, and documentation to ensure compliance.
• Review and approve batch records, validation reports, and change control documentation.
• Investigate deviations, out‑of‑specification (OOS) results, and customer complaints, and implement corrective and preventive actions (CAPAs).
• Ensure all quality‑related activities are documented accurately.
• Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure product quality and compliance.
• Train personnel on quality assurance procedures and cGMP principles.
• Participate in regulatory inspections and audits by health authorities (BPOM, FDA).
• Stay up‑to‑date with evolving pharmaceutical regulations and industry best practices.
• Develop and monitor key quality metrics and performance indicators.
• Contribute to the continuous improvement of the Quality Management System (QMS).
• Assisting in supplier qualification and auditing activities.
• Release raw materials, intermediates, and finished products based on established quality criteria.

• Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biology, or a related life science discipline.
• Minimum of 5 years of experience in Quality Assurance or Quality Control within the pharmaceutical or biotechnology industry.
• Comprehensive knowledge of cGMP, GCP, GLP, and other regulatory guidelines.
• Proven experience in performing audits, investigating deviations, and managing CAPAs.
• Strong understanding of pharmaceutical manufacturing processes and analytical testing.
• Excellent analytical, problem‑solving, and decision‑making skills.
• Meticulous attention to detail and commitment to accuracy.
• Strong written and verbal communication skills in English and Bahasa Indonesia.
• Proficiency in Microsoft Office Suite and experience with QMS software is a plus.
• Ability to work effectively both independently and as part of a cross‑functional team.

Senior Sanitation Quality Assurance Specialist – Remote

• Develop, implement, and maintain comprehensive sanitation programs across all operational areas.
• Conduct regular audits and inspections of facilities, equipment, and processes to verify compliance.
• Stay abreast of industry best practices and emerging trends in sanitation and hygiene management.
• Train and educate staff on proper sanitation procedures and the importance of maintaining a hygienic environment.
• Collaborate with cross‑functional teams (operations, maintenance, regulatory affairs) to integrate effective sanitation strategies.
• Manage documentation, maintain records, and prepare reports on sanitation performance and audit findings.
• Apply knowledge of food safety regulations (HACCP, GMP) and their application in non‑food manufacturing environments.
• Analyze data, identify trends, and recommend corrective actions.
• Foster a culture of quality and safety throughout the organization.

• A bachelor’s degree in a related field is preferred.
• Working knowledge of products and services.
• In‑depth understanding of industry standards and company policies.
• Strong analytical and problem‑solving skills.
• Meticulous and diligent attributes.
• Great team player with the ability to work with minimal supervision.

Senior Pharmaceutical Quality Assurance Specialist

• Maintain and enhance the Quality Management System (QMS).
• Conduct internal audits and inspections.
• Oversee compliance with Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP).
• Review and approve batch records, investigate deviations and OOS results, and implement CAPAs.
• Participate in regulatory inspections.
• Develop and implement QA policies and procedures.
• Manage CAPA system and review manufacturing documentation.
• Provide point of contact for regulatory agencies during inspections.
• Act as an advocate for product quality reviews.
• Contribute to continuous improvement of the QMS.

• Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum 5 years of progressive experience in Quality Assurance within the pharmaceutical industry.
• Strong knowledge of pharmaceutical quality systems and regulatory affairs.
• Experience with sterile manufacturing or specific dosage forms is a plus.
• Excellent written and verbal communication skills.
• Proficient in document management and data analysis tools.

Quality Assurance Specialist – Mandarin Speaker at FireRock Holdings

• Execute manual and automated testing of game builds across multiple devices and platforms.
• Maintain a high level of test coverage across all features and game systems.
• Identify, document, and track bugs using issue‑tracking systems (Jira, Clickup).
• Collaborate closely with developers, designers, and producers to reproduce and isolate bugs.
• Perform regression, smoke, and sanity testing as part of release cycles.
• Validate game balance, UI flow, and localization across regions.
• Write clear and concise test cases, checklists, and QA documentation.
• Provide feedback from the player’s perspective to improve overall gaming experience.

• Fluent in Mandarin (spoken and written), minimum HSK 4 or equivalent.
• Bachelor’s degree in Computer Science, Game Design, or a related field.
• Proven experience in game QA testing (mobile, PC, or console).
• Strong attention to detail and analytical skills.
• Familiarity with bug‑tracking and test‑management tools.
• Basic understanding of game development processes and pipelines.
• Familiarity with Unity engine and version control tools.
• Ability to write and follow detailed test cases and report bugs clearly.
• Ability to work independently and as part of a team in a fast‑paced environment.
• Excellent communication and documentation skills.
• Passion for gaming and a solid understanding of different game genres and platforms.

• Knowledge of Unity, Unreal Engine, or other game engines.
• Knowledge of asset bundle workflows and runtime content delivery.
• Exposure to localization QA and multi‑language testing.

• Strategic role with real influence on growth and community engagement.
• Competitive salary and comprehensive private health insurance coverage.

Equal Opportunity Statement

FireRock is committed to building a diverse, inclusive team where diverse voices make us stronger. We know creativity and effective problem‑solving come from teams that reflect many backgrounds, perspectives, and experiences. Together, we’re building games and communities that matter.