48 Quality Assurance jobs in Jakarta

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The Associate Software Quality Assurance / Testing Engineer is an entry level subject matter expert, responsible for assisting with every phase of the development process to ensure that the design and software adhere to company standards.
This role provides support in the development and execution of exploratory and automated tests to ensure product quality.
**What you'll be doing**
**Key Responsibilities:**
+ Supports the planning, execution, reporting, and successful completion of QA activities for all new development cycles for various releases.
+ Assists in Agile-related user story review meetings and/or works with relevant business stakeholders and developers to understand the new or modified application functionality.
+ Receives detailed instructions to work with the required user community (such as Regions or the Product Owner) to understand business requirements and uphold quality of for each release by ensuring a comprehensive end-to-end testing coverage.
+ Assists with designing and implementing end-to-end test scenarios, as well as debugging and defining corrective actions.
+ Supports the review of system requirements and tracking of quality assurance metrics (e.g. defect densities and open defect counts).
+ Assists with performing and documenting risk analysis and records test progress and results. Performing thorough regression testing when bugs are resolved.
+ Takes direction from various stakeholders to review requirements, specifications, and technical design documents to provide timely and meaningful feedback.
+ Assists with the creation of detailed, comprehensive, and well-structured test plans and test cases.
+ Supports the design, development, coding, and execution of automation scripts
+ Receives detailed instructions to identify, record, document thoroughly, and track bugs and develop and apply testing processes for new and existing products to meet client needs.
+ Assists with the development of standards and procedures to determine product quality and release readiness.
+ Supports and documents established QA processes and best practices in Agile Scrum development methodology and influences the continuous improvement of the QA activities.
+ Performs any other related task as required.
**Knowledge and Attributes:**
+ Some expertise in software QA methodologies, tools, and processes.
+ Interpersonal, communication, and organizational skills.
+ Team player with good attention to detail.
+ Ability to understand and analyze complex systems
+ Some understanding of SQL and scripting.
+ Some understanding of software development process.
+ Some expertise in agile development such as Scrum.
+ Some understanding of software integrated development environments.
+ Ability to handle client and customer issues tactfully and professionally.
+ Some understanding of object-oriented programming.
**Academic Qualifications and Certifications:**
+ Bachelor's degree or equivalent in Computer Science, Engineering or a related field.
+ Relevant certifications such as Leading SAFe would be advantageous.
**Required Experience:**
+ Basic hands-on testing experience in AGILE/DevOps Methodology, Continuous Integration, and Continuous Delivery.
+ Basic work experience in software development.
+ Basic work experience in software quality assurance.
+ Familiarity with working in an Agile/Scrum development process.
+ Familiarity with performance and/or security testing is a plus.
+ Basic hands-on experience with automated testing tools.
+ Basic experience working within a geographically dispersed company is desirable.
**Workplace type** **:**
On-site Working
**About NTT DATA**
NTT DATA is a $30+ billion trusted global innovator of business and technology services. We serve 75% of the Fortune Global 100 and are committed to helping clients innovate, optimize and transform for long-term success. We invest over $3.6 billion each year in R&D to help organizations and society move confidently and sustainably into the digital future. As a Global Top Employer, we have diverse experts in more than 50 countries and a robust partner ecosystem of established and start-up companies. Our services include business and technology consulting, data and artificial intelligence, industry solutions, as well as the development, implementation and management of applications, infrastructure, and connectivity. We are also one of the leading providers of digital and AI infrastructure in the world. NTT DATA is part of NTT Group and headquartered in Tokyo.
**Equal Opportunity Employer**
NTT DATA is proud to be an Equal Opportunity Employer with a global culture that embraces diversity. We are committed to providing an environment free of unfair discrimination and harassment. We do not discriminate based on age, race, colour, gender, sexual orientation, religion, nationality, disability, pregnancy, marital status, veteran status, or any other protected category. Join our growing global team and accelerate your career with us. Apply today.

Title:
Quality Assurance Lead
Primary Functions
Safe, effective, and quality delivery of the assigned Project Assurance activities in support of Quality / Project Manager (FEED Phase)
Tasks and Responsibilities
+ Responsible for Jakarta quality function and assigned project quality activities,
+ Promote the Quality and Compliance requirements within the project team and client interface,
+ Support to development, implementation, and maintenance of the Project Quality Plan,
+ Coordinate and manage quality and compliance across the project team, provide support and guidance,
+ Establish network with other Company project quality groups to ensure best practices / lessons learnt are employed and captured and disseminated to Project Team members,
+ Effectively manage quality compliance audit and surveillance program in accordance with generated plans, ensure outputs from these activities are reported and disseminated to project team members,
+ Champion quality and compliance requirements within Project Team and Supply Chain organizations,
+ Work with delivery, engineering, procurement, and client team to resolve quality issues,
+ Play an active role in ensuring that all project activities comply with required Company safety, environmental and ethical standards,
+ Take time to ensure personal safety and recognize safety concerns for fellow team members, reporting potential safety issues and unsafe acts. Courage to Care.
+ Provide support to occupational Health and Safety manager within Jakarta Office remit
Experience
+ 10 to 15 Years as Quality Assurance with EPC Organization preferred
+ Minimum bachelor's degree
+ Lead Auditor Certification (ISO)
Location
+ Jakarta

Our client is looking for a meticulous and dedicated Pharmaceutical Quality Assurance Specialist to join our regulatory compliance team in **Jakarta, Jakarta, ID**. This role is critical in ensuring that our pharmaceutical products meet the highest standards of quality, safety, and efficacy, adhering to all national and international regulatory requirements. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS). This includes conducting internal audits, reviewing manufacturing processes, and ensuring compliance with Good Manufacturing Practices (GMP). Your responsibilities will extend to investigating deviations, managing corrective and preventive actions (CAPA), and participating in regulatory inspections. Excellent analytical skills and a thorough understanding of pharmaceutical manufacturing processes and quality control principles are essential. The ideal candidate will possess strong documentation skills and the ability to interpret and apply regulatory guidelines effectively. You will work collaboratively with manufacturing, R&D, and validation teams to resolve quality issues and drive continuous improvement. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field is required. At least 4 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry is mandatory. Knowledge of GMP, regulatory affairs, and quality risk management is essential. Strong attention to detail, problem-solving capabilities, and excellent written and verbal communication skills are necessary. This position is based in **Jakarta, Jakarta, ID**, and requires full-time commitment on-site. Join our team and contribute to delivering life-saving medicines with unwavering quality.

Our client is seeking an experienced Senior Quality Assurance Engineer to join their manufacturing and production team in **Jakarta, Jakarta, ID**. This role requires on-site presence to oversee and implement quality control processes directly on the production floor. You will be responsible for developing and executing comprehensive quality assurance strategies, ensuring that all manufactured products meet stringent quality standards and customer specifications. Your duties will include designing and implementing test plans, developing testing procedures, and conducting rigorous testing of raw materials, in-process materials, and finished goods. You will analyze quality data, identify root causes of defects, and implement corrective and preventive actions (CAPA). Collaborating with production, engineering, and R&D teams is crucial to address quality issues and drive continuous improvement. You will also be responsible for maintaining quality documentation, ensuring compliance with industry standards (e.g., ISO), and training production staff on quality procedures. The ideal candidate will possess a Bachelor's degree in Engineering (Mechanical, Industrial, or relevant field), with a minimum of 5 years of experience in quality assurance within a manufacturing environment. Strong knowledge of quality management systems (QMS), statistical process control (SPC), and various testing methodologies is required. Excellent analytical, problem-solving, and communication skills are essential. Experience with Six Sigma or Lean Manufacturing principles is a significant advantage. This position offers a vital role in ensuring the high quality of our client's products.

Our client is seeking a highly experienced and meticulous Pharmaceutical Quality Assurance Manager to ensure the highest standards of product quality and regulatory compliance. This is a fully remote position, offering the flexibility to manage quality systems from anywhere in Indonesia. You will be responsible for developing, implementing, and maintaining the company's Quality Management System (QMS) in accordance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines. Key responsibilities include overseeing quality control processes, conducting internal audits, managing deviations and CAPAs (Corrective and Preventive Actions), and ensuring all pharmaceutical products meet specified quality standards. You will also be involved in validating manufacturing processes and equipment, managing batch record reviews, and leading regulatory inspections. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing, quality assurance principles, and regulatory requirements. Excellent leadership, analytical, and problem-solving skills are essential. Key Duties:

• Develop and implement robust Quality Management Systems (QMS) compliant with GMP standards.
• Oversee quality control testing and product release processes.
• Manage deviations, investigations, and CAPA systems to address quality issues.
• Conduct internal audits to ensure compliance with regulations and company procedures.
• Lead and participate in external regulatory inspections (e.g., BPOM).
• Review and approve batch manufacturing records and validation documentation.
• Train and mentor quality assurance personnel.
• Collaborate with R&D, production, and regulatory affairs teams to ensure product quality throughout the lifecycle.

Qualifications:

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related science field.
• Minimum of 8 years of experience in pharmaceutical quality assurance or quality control, with at least 3 years in a management role.
• In-depth knowledge of GMP, ICH guidelines, and Indonesian pharmaceutical regulations.
• Experience with pharmaceutical manufacturing processes and analytical testing.
• Proven ability to manage a Quality Assurance team and drive continuous improvement.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong communication and leadership abilities.
• Comfortable working independently and managing quality operations in a remote setting.

This is a vital role for ensuring the integrity of pharmaceutical products. If you are a dedicated QA professional looking to lead quality initiatives in a remote-first environment, we encourage you to apply.

We are seeking a meticulous and experienced Pharmaceutical Quality Assurance Manager to oversee our quality systems and compliance efforts. This role offers a fully remote working arrangement, allowing you to contribute to critical quality functions from your home office. You will be responsible for developing, implementing, and maintaining comprehensive quality assurance programs that ensure compliance with GMP, FDA, and other relevant regulatory standards. Your duties will include conducting internal audits, reviewing batch records, investigating deviations and out-of-specifications results, and managing change control processes. You will also play a key role in preparing for and hosting regulatory inspections, ensuring that all documentation is accurate and up-to-date. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, quality control principles, and regulatory requirements. Excellent analytical and problem-solving skills, coupled with meticulous attention to detail, are essential for this role. You will collaborate closely with various departments, including R&D, manufacturing, and regulatory affairs, to ensure consistent product quality and compliance. Experience in developing and validating analytical methods, as well as a strong grasp of statistical analysis, will be highly beneficial. This position requires a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field, along with a proven track record in pharmaceutical quality assurance. You must be a proactive individual with the ability to work independently, manage multiple projects, and meet strict deadlines in a remote setting. Join our dedicated team and contribute to delivering safe and effective pharmaceutical products to the market.

Our client is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Assurance Specialist to ensure the highest standards of quality and compliance within their operations. This role is essential for maintaining the integrity of our pharmaceutical products and processes. You will be responsible for developing, implementing, and maintaining robust quality systems, conducting audits, and ensuring adherence to regulatory guidelines such as GMP (Good Manufacturing Practice). The ideal candidate will possess a strong scientific background, exceptional attention to detail, and a thorough understanding of pharmaceutical manufacturing and regulatory affairs. This position requires on-site presence to effectively oversee critical quality control and assurance activities.

Key Responsibilities:

• Develop, implement, and maintain comprehensive quality assurance systems.
• Conduct internal and external audits to ensure compliance with GMP and other regulatory standards.
• Review and approve batch records, validation protocols, and other quality-related documentation.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints.
• Implement corrective and preventive actions (CAPA) to address quality issues.
• Monitor and assess the performance of quality control laboratories and manufacturing processes.
• Provide training to personnel on quality systems and GMP requirements.
• Stay updated on pharmaceutical regulations and industry best practices.
• Participate in regulatory inspections and collaborate with health authorities.
• Contribute to the continuous improvement of quality processes and procedures.
• Prepare and present quality metrics and reports to management.

Qualifications:

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 6 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
• In-depth knowledge of GMP, ICH guidelines, and other relevant regulatory requirements.
• Proven experience in conducting audits and managing CAPA systems.
• Strong analytical and problem-solving skills.
• Excellent written and verbal communication skills.
• Ability to work independently and as part of a team.
• Proficiency in quality management software and data analysis tools.
• Attention to detail and a commitment to maintaining high quality standards.
• Experience in pharmaceutical manufacturing processes is highly desirable.

If you are a dedicated quality professional with a passion for ensuring product safety and efficacy in the pharmaceutical sector, we encourage you to apply. Join our client's team and play a vital role in their commitment to excellence.

Our client, a globally recognized pharmaceutical company, is seeking a highly skilled and dedicated Senior Pharmaceutical Quality Assurance Manager to lead their quality operations. This is a fully remote position, offering the flexibility to contribute from anywhere. You will be responsible for developing, implementing, and maintaining the company's quality management system (QMS) to ensure compliance with regulatory requirements such as GMP, ICH guidelines, and other relevant standards. Your core duties will include overseeing quality control processes, managing internal and external audits, conducting investigations of deviations and non-conformances, and implementing CAPA (Corrective and Preventive Actions). You will also play a key role in product lifecycle management, regulatory submissions, and continuous improvement initiatives. The ideal candidate will have extensive experience in the pharmaceutical industry, with a proven track record in quality assurance or quality control roles. Strong knowledge of pharmaceutical manufacturing processes, regulatory affairs, and quality systems is essential. Excellent leadership, communication, problem-solving, and analytical skills are required to effectively manage a team and interact with cross-functional departments and regulatory bodies. A Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field is required, with a Master's degree or advanced certification being a significant advantage. Join our client to ensure the highest standards of quality and safety in life-saving medicines.

Our client, a prominent Pharmaceutical company, is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Assurance Specialist to join their team in Jakarta, Jakarta, ID . This critical role is responsible for upholding the highest standards of quality and compliance throughout the pharmaceutical manufacturing process, ensuring adherence to Good Manufacturing Practices (GMP) and regulatory requirements.

The Senior Pharmaceutical Quality Assurance Specialist will oversee quality control activities, review and approve batch records, investigate deviations and out-of-specification results, and implement corrective and preventive actions (CAPA). You will be involved in internal and external audits, process validation, and ensuring all documentation meets regulatory agency standards. This position requires a deep understanding of pharmaceutical quality systems and a commitment to maintaining product integrity and patient safety.

Key responsibilities include:

• Reviewing and approving batch production and control records to ensure compliance with specifications and procedures.
• Investigating deviations, out-of-specification (OOS) results, and customer complaints.
• Developing and implementing Corrective and Preventive Actions (CAPA) plans.
• Participating in internal and external audits, including regulatory inspections (e.g., BPOM).
• Ensuring all manufacturing processes and documentation comply with cGMP guidelines.
• Conducting process validation, cleaning validation, and equipment qualification activities.
• Developing and maintaining Standard Operating Procedures (SOPs) and other quality-related documents.
• Monitoring and analyzing quality data to identify trends and areas for improvement.
• Providing training to personnel on quality assurance principles and procedures.
• Collaborating with cross-functional teams, including production, R&D, and regulatory affairs.

The ideal candidate will have a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 5-7 years of experience in Quality Assurance within the pharmaceutical industry is mandatory. Strong knowledge of GMP regulations, quality management systems, and pharmaceutical manufacturing processes is essential. Experience with auditing, CAPA systems, and validation protocols is required. Excellent analytical, problem-solving, and documentation skills are critical. Strong communication and interpersonal skills are necessary to effectively interact with team members and regulatory bodies. This is an excellent opportunity to contribute to a company dedicated to producing high-quality pharmaceuticals.