CrawlJobs Logo
NTT DATA Logo NTT DATA · IT - Software Development

Quality Assurance

Indonesia, Jakarta Selatan · Job Posted June 29, 2026
Apply Position
Job Link Share

Job Description

The Software Quality Assurance / Testing Engineer is a seasoned subject matter expert, responsible for participating in every phase of the development process to ensure that the design and software adhere to company standards. This role collaborates with various stakeholders in the development and execution of exploratory and automated tests to ensure product quality.

Job Responsibility

  • Develop, execute, and maintain automated test scripts using Katalon Studio
  • Perform functional, regression, and integration testing
  • Works across multiple teams to ensure the planning, execution, reporting, and successful completion of QA activities for all new development cycles for various releases
  • Contributes to Agile-related user story review meetings and/or work with relevant business stakeholders and developers to understand the new or modified application functionality
  • Networks with the required user community (such as Regions or the Product Owner) to understand business requirements and uphold quality of each release by ensuring a comprehensive end-to-end testing coverage
  • Designs and implements end-to-end test scenarios, as well as debugging and defining corrective actions
  • Contributes to performing and documenting risk analysis and record test progress and results
  • Performing thorough regression testing when bugs are resolved
  • Works across multiple teams to review requirements, specifications, and technical design documents to provide timely and meaningful feedback
  • Creates detailed, comprehensive, and well-structured test plans and test cases
  • Designs, develops, codes, and executes automation scripts
  • Works across multiple teams to identify, record, document thoroughly, and track bugs and develop and apply testing processes for new and existing products to meet client needs
  • Develops standards and procedures to determine product quality and release readiness
  • Contributes recommendations that will enable innovation and streamline overall testing processes
  • Works across multiple teams, documenting established QA processes and best practices in Agile Scrum development methodology and influence the continuous improvement of the QA activities
  • Performs any other related task as required

Requirements

  • 2–4 years of experience in QA / Software Testing
  • Strong hands-on experience with Katalon Studio (mandatory)
  • Solid understanding of SDLC and STLC
  • Experience in test automation and manual testing
  • Familiar with API testing tools (e.g., Postman)
  • Strong analytical thinking and attention to detail
  • Good communication skills and teamwork
  • Bachelor's degree or equivalent in Computer Science, Engineering or a related field

Nice to have

  • Proficiency with performance and/or security testing is a plus
  • Seasoned experience working within a geographically dispersed company is desirable
NTT DATA - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Quality Assurance

8 matching positions

Quality Assurance

We are seeking a detail-oriented QA professional to ensure accuracy and consiste...
Location
Location
Bangladesh , Dhaka
Salary
Salary:
Not provided
aithoth.com Logo
Thoth AI
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Diploma or bachelor’s degree in any field (preferred in Linguistics, Communication, or related disciplines)
  • Proficient in English
  • Prior experience in QA position in data labelling, content moderation, or annotation projects is an advantage
  • Attention to detail and Ability to follow complex guidelines
  • Quick to adapt to guideline changes
Job Responsibility
Job Responsibility
  • Review daily samples of agents’ tasks to ensure quality and identify errors
  • Act as the arbitrator in the ROCK system to verify the correctness of disputed cases and ensure the final decision aligns with policy
  • Track agents’ accuracy on a daily basis and flag any risks or drops in performance
  • Join calibration sessions with BDQA to ensure consistent policy understanding across the team
  • Provide regular coaching and constructive feedback to help agents improve their quality
  • Prepare or update reports and documentation required for quality monitoring and operational alignment
  • Annotating data related to audio, captions, and photos in order to identify potential violations within a piece of content
  • Collaborating with the QA, and another team member to ensure the project going smoothly
  • Maintaining quality, productivity, and utilization rate as defined by the project
  • Fulltime
Read More
Arrow Right

Quality Assurance

Job Title: Quality Assurance. Duration: 10 months. Location: Newark DE. Module: ...
Location
Location
United States , Newark
Salary
Salary:
55.00 - 60.42 USD / Hour
apexsystems.com Logo
Apex Systems
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 8+ years of experience in QA testing
  • Knowledge and working experience on Agile testing Methodology
  • Hands-on experience in Web Services testing including Soap UI/XML, REST/JSON, MQ and Unix
  • Experience on Frontend, ETL and Database testing, with extensive working experience in writing and executing SQL queries
  • Unix, SQL Putty, Soap UI, WinSCP App Watch MQ, Splunk, JBoss. Autosys, TOAD, HP ALM JIRA
  • 2+ years of Selenium Automation experience
  • Log validations experience or Files validation manually
  • Unix commands experience
Job Responsibility
Job Responsibility
  • Key individual contributor to Quality Assurance Project teams and/or Lines of business
  • Works with project teams to ensure standard quality practices/processes are followed
  • Performs SIT/End-to-end testing on applications and technology
  • Designs and Executes test scripts based upon test strategy/plans
  • May also include Production Certification which requires manual/automated scripts be executed to certify production health and/or identify post-production defects
What we offer
What we offer
  • Medical, dental, vision, life, disability, and other insurance plans
  • ESPP (employee stock purchase program)
  • 401K program with company match after 12 months
  • HSA (Health Savings Account on the HDHP plan)
  • SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions
  • Corporate discount savings program
  • On-demand training program
  • Access to certification prep and a library of technical and leadership courses/books/seminars after 6+ months
  • Certification discounts
  • Dedicated customer service team
  • Fulltime
Read More
Arrow Right

Quality Assurance

Location
Location
Ireland , Dublin
Salary
Salary:
Not provided
sgsco.com Logo
Executive Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Engineering or Life Science related discipline
  • 2+ years of Quality Assurance experience in a Life Sciences environment
  • Manage internal ISO quality process
  • Understanding of principles of Validation and New Product Introduction
  • Experience in change control, non-conformance, corrective and preventative actions, and validation practices
  • Proven experience participating in or leading audits and inspections
Job Responsibility
Job Responsibility
  • Provide overall quality direction and oversight for key functional areas (i.e. Inspection, Validation, Quality Control, Engineering, ), ensuring that programs, policies and procedures are robust and in keeping with regulatory and company expectations
  • Quality review and approval of Validation documentation and SOPs to support site validation activities: Review of DS & QRAES documents
  • Review of validation Plans, Protocols, IQ, OQ, PQ and associated validation documents
  • Review of executed validation documents and reports
  • Support a safe working environment by complying with all pertinent environmental health/safety practice, rules and regulations
  • Provide Quality direction and input at Change Control and Deviation Review Boards and assume QA oversight of change control and Deviation/CAPA records
  • ensuring scope of record is clear and implementation activities are robust and timely
  • Perform all activities in compliance with company safety standards and SOPs
  • Fulltime
Read More
Arrow Right

Head Of Quality Assurance / Quality Control

We're partnered with a consumer products manufacturer that is looking for a Head...
Location
Location
United States , Santa Ana
Salary
Salary:
100000.00 - 135000.00 USD / Year
strategicemployment.com Logo
Strategic Employment Partners
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Hands-on QMS build or rebuild experience in a manufacturing environment
  • GMP experience — applied on the floor, not just theoretical
  • 5+ years managing or supervising QC teams (direct or indirect)
  • Production floor inspection experience — enforcing customer and internal spec compliance
  • Data fluency — KPIs, defect tracking, scrap/yield metrics, presenting to leadership
  • Experience handling customer quality disputes and documenting corrective actions
  • Onsite availability in Santa Ana
Job Responsibility
Job Responsibility
  • Own their quality department from the ground up, formalizing their QMS, installing inspection protocols on the production floor, and building the accountability structures their QC team needs to operate off documented systems
  • Fulltime
Read More
Arrow Right

Product Assurance Quality Assurance Engineer

Are you experienced in quality or product assurance within high-reliability engi...
Location
Location
Ireland , Dublin
Salary
Salary:
55000.00 - 85000.00 EUR / Year
morson.com Logo
Morson Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree in Engineering, Physics, or a related technical discipline (or equivalent experience)
  • Experience in a Product Assurance, Quality, or Reliability role within a high-reliability engineering environment
  • Strong knowledge of relevant industry standards (e.g. ECSS, ISO 9001, AS9100)
  • Understanding of electronics manufacturing, PCB assembly, and testing processes
  • Experience managing non-conformances and applying problem-solving methodologies
  • Ability to interpret technical drawings, specifications, and test requirements
  • Strong attention to detail with a structured, analytical approach
  • Excellent communication skills and ability to work across multidisciplinary teams
Job Responsibility
Job Responsibility
  • Defining and implementing PA/QA plans in line with customer and industry standards (e.g. ECSS, ISO)
  • Supporting design reviews, ensuring quality, reliability, and safety requirements are met
  • Leading and contributing to product assurance reviews at key project milestones
  • Overseeing manufacturing and assembly processes to ensure compliance with approved procedures and workmanship standards
  • Managing non-conformances, including root cause analysis and corrective/preventative actions
  • Reviewing and approving technical documentation such as procedures, inspection plans, and test reports
  • Supporting supplier quality assurance activities, including audits and performance monitoring
  • Participating in internal and external audits
  • Performing hardware inspections and producing quality reports
  • Ensuring configuration control and full traceability of materials and components
  • Fulltime
Read More
Arrow Right

Senior Manager Quality Assurance: Incoming Quality and Warehouse

At Amgen, if you feel like you’re part of something bigger, it’s because you are...
Location
Location
United States , New Albany
Salary
Salary:
144021.45 - 194852.55 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree and 2 years of Quality/Manufacturing/Engineering experience
  • Master's degree and 6 years of Quality/Manufacturing/Engineering experience
  • Bachelor's degree and 8 years of Quality/Manufacturing/Engineering experience
  • Associate's degree and 10 years of Quality/Manufacturing/Engineering experience
  • High school diploma / GED and 12 years of quality/Manufacturing/Engineering experience
  • minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources
Job Responsibility
Job Responsibility
  • Lead, coach and develop the QA team, responsible for quality oversight of Incoming Quality, Warehouse Operations, Distribution and Facility and Engineering. Team scope includes disposition of product, materials and components, including on-the-floor support, record review, quality oversight of deviation investigations and changes, document approval
  • Ensure AOH product is manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Amgen standards, and applicable regulations
  • Drive investigations and resolution of deviations, ensuring timely, thorough, and compliant outcomes
  • Lead and participate in Quality Risk Assessments
  • Provide Quality input to support project or operational design decisions
  • Build organization according to hiring strategy that supports our growth. Partner with HR to recruit, coach, develop, motivate, and retain staff. Ensure ongoing organizational structure capable of adapting to evolving business needs
  • Provide oversight to ensure that Amgen Quality Management System is implemented and maintained in accordance with corporate standards
  • Track performance and drive continuous improvement in the performance and delivery of quality outputs in alignment with Quality strategies
  • Develop strategies in support of regulatory inspections and site audits
  • Serve as quality representative to regulatory authorities, Amgen Corporate auditors, and 3rd Parties
What we offer
What we offer
  • health and welfare plans for staff and eligible dependents
  • financial plans with opportunities to save towards retirement or other goals
  • work/life balance
  • career development opportunities
  • comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • discretionary annual bonus program
  • stock-based long-term incentives
  • award-winning time-off plans
  • flexible work models where possible
  • Fulltime
Read More
Arrow Right

Lead Quality Assurance Engineer, Supplier Quality

The Lead Quality Assurance Engineer, Supplier Quality will provide supplier rela...
Location
Location
United States , Madison
Salary
Salary:
112000.00 - 190000.00 USD / Year
exactsciences.com Logo
Exact Sciences
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in a Science or technical field
  • or Associate’s degree in Science or technical field and 2 years of relevant experience as outlined in the essential duties in lieu of a Bachelor’s degree
  • 5+ years of experience in quality principles and practice including experience in assigned area (Design Control, Supplier Management, Risk Management, etc.)
  • Product Development assignments require 8+ years of experience in product development in the medical device industry with experience in complex systems including software
  • Design Transfer assignments require 8+ years of experience in process validation principles and practice
  • Manufacturing Support assignments require 8+ years of experience in a manufacturing operation environment
  • Demonstrated ability to successfully work within an CFR 820, ISO 13485, ISO 9001, and/or cGMP structured environment
  • Applicants must be currently authorized to work in country where work will be performed on a full or part-time basis
  • Demonstrated ability to perform the Essential Duties of the position with or without accommodation
Job Responsibility
Job Responsibility
  • Represent Quality on a variety of projects as assigned
  • Communicate and collaborate with business partners to ensure robust materials, products, processes, and systems and compliance to procedures and specifications
  • Create documentation and records in the Electronic Quality Management System (EQMS)
  • Perform risk assessments and provide risk mitigation strategies
  • Implement processes to monitor product and process performance, compliance, and reliability
  • Implement, conduct, and report on process quality programs using statistical data analysis
  • Review and approve documentation related to Exact Sciences products
  • Conduct periodic reviews of Quality System documentation
  • Generate and distribute Quality metrics as assigned
  • Generate, prepare, and issue data for assigned quality plans
What we offer
What we offer
  • Paid time off (including days for vacation, holidays, volunteering, and personal time)
  • Paid leave for parents and caregivers
  • A retirement savings plan
  • Wellness support
  • Health benefits including medical, prescription drug, dental, and vision coverage
  • Bonus eligibility
  • Fulltime
Read More
Arrow Right

Senior Director, Quality Assurance

Theradaptive is revolutionizing the field of therapeutic delivery with a pipelin...
Location
Location
United States , Frederick
Salary
Salary:
Not provided
Theradaptive
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree (required) in Life Sciences, Biomedical Engineering, Chemistry, Biochemistry, or a related field
  • Advanced degree (M.S., Ph.D., or M.D.) strongly preferred
  • 15+ years of progressive quality experience in the biopharmaceutical, biotech, or medtech industry, with at least 5 years in a senior leadership role (Director level or above)
  • Demonstrated experience with combination products, including working knowledge of both drug/biologic and device QMS frameworks
  • Direct experience managing FDA inspections (PAI, cGMP, QSR) and responding to 483 observations and Warning Letters
  • Hands-on experience with protein biologics or growth factors (e.g., rhPDGF, BMP, FGF, EGF, VEGF) in a GMP manufacturing or quality context
  • Experience with sterile or aseptic combination products is highly preferred
  • Expert-level knowledge of: 21 CFR Parts 210/211 (Drug cGMP), 21 CFR Part 820 / ISO 13485 (Device QMS), 21 CFR Part 4 (Combination Products)
  • Expert-level knowledge of: ICH Q7, Q8, Q9, Q10, Q11 guidelines
  • Expert-level knowledge of: ISO 14971 (Risk Management), ISO 10993 (Biocompatibility)
Job Responsibility
Job Responsibility
  • Design, implement, and own an integrated QMS that satisfies 21 CFR Parts 210/211 (drug/biologic GMP), 21 CFR Part 820 / ISO 13485:2016 (medical device QMS), and ICH guidelines (Q7, Q8, Q9, Q10)
  • Ensure the QMS addresses the regulatory designation of the combination product (PMOA-based lead center: CDRH or CDER) and the requirements of the non-lead center
  • Develop and maintain all quality policies, SOPs, work instructions, and quality plans across the product lifecycle
  • Drive QMS digital transformation initiatives, including electronic quality management platforms (e.g., Veeva Vault QMS, MasterControl, TrackWise)
  • Serve as the company's subject-matter expert on 21 CFR Part 3 (combination product designation), 21 CFR Part 4 (regulation of combination products), and applicable guidance documents
  • Lead cross-functional efforts to align quality requirements for both the protein growth factor drug/biologic constituent and the device constituent part throughout CMC development, scale-up, and commercialization
  • Oversee the integration of device design controls (21 CFR 820.30) with drug development quality requirements, ensuring alignment in risk management activities per ISO 14971
  • Collaborate closely with Regulatory Affairs on BLA, PMA, 510(k), or De Novo submission strategies — specifically quality module content (Module 3 / CTD, Design History File, Device Master Record)
  • Prepare and lead quality-related FDA interactions including pre-submission meetings, Agency responses, and inspection readiness activities
  • Support compliance with EU MDR 2017/745, IVDR, and country-specific registration requirements for international expansion
Read More
Arrow Right