Manual QC (Data Testing) Job at Amaris Consulting (Ho Chi Minh City)

QA/QC Engineer

Perform manual and automation testing to ensure software quality, reliability, s...

Location

Vietnam , Ho Chi Minh City

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Information Technology, Software Engineering, Computer Science, or a related field
From 2 to 3+ years of experience in software testing or quality control
Hands-on experience in both manual testing and automation testing
Strong experience in automation testing using Selenium
Good understanding of testing methodologies, test design techniques, and software testing lifecycle
Experience in writing and executing test cases, test scenarios, test plans, and defect reports
Experience with functional testing, regression testing, integration testing, smoke testing, and sanity testing
Familiarity with programming or scripting languages such as Java, Python, JavaScript, or C# for automation testing
Experience with test management and bug tracking tools such as Jira, Azure DevOps, TestRail, or similar tools
Basic understanding of SQL, API testing, or Postman is an advantage

Job Responsibility

Perform manual and automation testing to ensure software quality, reliability, scalability, and security
Analyze business requirements, functional specifications, and technical documents to understand testing scope and test coverage
Design, prepare, and execute test cases, test scenarios, and test data for web and/or mobile applications
Develop and maintain automation test scripts using Selenium and related testing frameworks
Perform functional testing, regression testing, integration testing, smoke testing, and sanity testing
Identify, report, track, and verify defects throughout the testing lifecycle
Work closely with developers, Business Analysts, Product Owners, and project teams to clarify requirements and resolve quality issues
Support defect investigation and provide clear evidence, logs, screenshots, and reproduction steps
Estimate testing effort and support test planning activities

What we offer

Competitive salary and 13th-month salary
14+ annual leaves per year
Premium healthcare insurance, starting from your probation period
Project reviews and yearly performance appraisal
Annual company trips
Teambuilding activities: Team lunch/dinner, events, and celebrations, sports clubs (football, basketball, badminton, pickleball)
International team with flexible working time
Tailor-made career path
Technical workshops and training courses
Mobility: Opportunities to be on-site abroad in our offices in over 60+ countries

Fulltime

Microbiologist I

Argenta is currently looking to fill the role of Microbiologist I at our Shawnee...

Location

United States , Shawnee

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

BA / BS in a related scientific field such as biology, chemistry, microbiology, or biochemistry
1+ year laboratory experience, which can include academic experience or microbiology laboratory
basic background for the understanding, planning, and execution of laboratory Standard Operating Procedures relating to instrument use, sample analysis, document generation and control, personal safety, and environmental safety
Knowledge of FDA regulations (or similar regulated environment) to include Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP)
Basic computer skills are required
Must be able to pass a DEA background check
Proven, effective written and verbal communication skills
Demonstrated skills in the use of a wide range of microbiology test methods and instrumentation, including the following: Bioburden testing
Endotoxin testing
Aseptic technique

Job Responsibility

Performs testing of raw material, in-process and finished product samples according to approved procedures
Perform Environmental monitoring of the manufacturing and laboratory facilities including cleanroom environments, personnel, water systems, compressed gases, and laminar flow hoods
Identify microbial isolates using manual or automated techniques per written procedures in a timeframe that supports customer requirements
Prepares media, solutions, materials and equipment to support sampling and testing
Performs growth promotion and quality testing on media used for microbiological testing, and environmental monitoring in the Microbiology QC Department as needed
Maintain the record storage systems in a manner that ensures quick and reliable retrieval of the data as needed
Provide support to laboratory projects and assist other team members as needed
Adhere to the pertinent aspects of compliance and plant safety programs
Critical understanding of proper and thorough laboratory investigations
Support QA Operations as required for laboratory investigations

What we offer

great benefits
opportunity for growth

Fulltime

Senior Associate - QC Technical Services

Supporting the technical services team, the Senior Associate is responsible for ...

Location

Ireland , Dun Laoghaire

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a Science related field is required
Minimum of 5 + years of laboratory experience in a cGXP laboratory environment including exposure to analytical instrument validation
Detailed knowledge of the methodology and instrumentation and analytical techniques used for biopharmaceutical testing
Understanding of current regulatory requirements for cGXP laboratory equipment validation and electronic record integrity
Demonstrated success in managing an equipment qualification or maintenance program advantageous

Job Responsibility

Supporting the Quality Control Laboratories, the System Owner is responsible for the complete life cycle of QC equipment
Select and procure laboratory equipment in accordance with Amgen requirements
Owns and project manages change controls and adhere to Change Control metrics
Planning, executing and documenting the qualification of new laboratory equipment in a cGxP regulated environment
Developing and maintaining an equipment qualification project plan, requirements, qualification protocols and summary reports as part of the commissioning of new laboratory equipment
Generation and resolution of protocol deviations as required
Writing/contributing to equipment operating procedures and manuals
Designing and conducting training for QC staff, and other department staff as applicable
Developing and maintaining Data Integrity Assessments for QC laboratory systems
Conduct periodic reviews of instrument validation as part of validation life cycle

Fulltime

QA/qc technician

Under the direction of the Compost Manager/Supervisor, you will be responsible f...

Location

Canada , Niagara Falls

Salary:

50000.00 - 55000.00 CAD / Year

Walker Industries

Expiration Date

Until further notice

Requirements

Experience in a laboratory, production setting and/or operational environments is considered an asset. Equivalent combination of education, training, and hands-on experience will be considered.
Graduation from college in a related field such as biology, chemistry or environmental science/management is considered an asset.
Demonstrated willingness and ability to learn technical processes, procedures, and systems.
Strong communication, problem-solving, and organizational skills with the ability to work independently and as part of a team.
A valid driver’s license and reliable transportation.
Experience with Microsoft Word and Excel.

Job Responsibility

Perform tasks in the areas of sample collection/preparation, resampling, and chemical analysis.
Laboratory maintenance, entering data from lab reports, ordering/purchasing lab and general supplies.
Overseeing curing piles to identify when piles are ready for sampling.
Test and record physical and chemical properties such as moisture, pH level, temperatures and porosity, bulk density and oxygen.
Collect and label ground and/or surface water samples from round the Niagara Campus.
Provides insight into and interpretation of results, collecting data where required and generating data for weekly, monthly and annual reports.
Comply with all regulatory requirements (Ministry of Environment) and company policies/procedures as they pertain to this position.
Assist in the development and maintenance of Safe Work Procedures.
Maintain legible and detailed records (manual and electronic).
Communicate needs of process changes to Compost Operators.

What we offer

A comprehensive total rewards package and benefits to support your wellbeing
Leaders who support your growth and success
A workplace that provides the best health & safety practices in industry
Give back to your community with two paid volunteer days annually and opportunities to become involved in events

Fulltime

Quality Control Analyst/Tester

We are seeking a Quality Control Analyst / Tester to work alongside a Business A...

Location

Canada , North York

Salary:

70000.00 - 90000.00 USD / Year

FARBER

Expiration Date

Until further notice

Requirements

4+ years in QC/testing roles with a blend of manual and automation testing
Demonstrated experience with Azure DevOps Test Management (test plans, test suites, test cases, defects, reporting)
Experience testing low-code / SaaS / web applications with complex workflows and data rules
Strong understanding of testing fundamentals: test design techniques, boundary/negative testing, regression approaches, and risk-based testing
Familiarity with automation tools/frameworks such as Playwright, Selenium, Cypress, or similar (tool-agnostic
prove ability to automate)
Ability to validate data and integrations (REST APIs, JSON payloads, connector outputs) using Postman or equivalent API query, debug and dev tools
Ability to validate outputs with independent queries using T-SQL, Fetch or equivalent data query methods
Solid communication skills and ability to work closely with developers and analysts

Job Responsibility

Define and maintain test strategy and test plans business application delivery (functional, regression, integration, data, security, performance)
Create and manage test suites, test cases, and test execution cycles in Azure DevOps Test Plans, ensuring traceability to backlog items
Design and build automated test scripts to support regression and critical-path validation (UI and/or API level)
Validate acceptance criteria with the Business Analyst and technical feasibility with the Architect
Perform end-to-end scenario testing across app → flow → data → integration surfaces
Log, triage, and track defects in Azure DevOps, including severity/prioritization recommendations and retest confirmation
Support release readiness by providing test completion reports, defect summaries, and go/no-go input
Participate in agile ceremonies (planning, refinement, demos, retros) and advise on test effort and risk early
Continuously improve QC practices: reusable test assets, automation coverage, and test data management

What we offer

Remote work model
Vacation and wellness days
Extended health and dental coverage, plus virtual doctor services
Employee Assistance Program and mental health resources
Company-matching retirement savings plan
Financial support for professional development
Annual company events
Exclusive access to perks and discounts

Fulltime

Coordinator Quality Assurance & Control

Under the direction of the Laboratory Director and in collaboration with the Lab...

Location

United States , Tucson

Salary:

Not provided

Tucson Medical Center

Expiration Date

Until further notice

Requirements

Bachelor's degree in Medical Laboratory Science or equivalent
Minimum of 5 years experience in a Clinical Laboratory
Must be able to train others to use CQI and related SPC tools
Medical Technologist (ASCP) Certification or equivalent
Knowledge of quality control test measurements and regulations regarding analyzing specimens
Skill in evaluating tests and identifying measures outside the norm, and whether any follow up testing might be required
Demonstrates effective computer skills including programs such as Microsoft Office Suite, email, PDF, and internet searches
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals
Ability to complete routine reports and correspondence
Ability to listen and accurately interpret others’ communication or instructions to take appropriate action

Job Responsibility

Supports quality improvement initiatives through team participation, data collection, process change implementations, and other activities
Ensures Quality Assurance Quality Control Program fulfills all accreditation and regulatory requirements of local, state and federal agencies and affiliates (e.g., CAP, JCAHO, CLIA, FDA, OSHA, AABB, etc.)
Provides and communicates current regulatory guidelines, legislative changes and accreditation criteria to laboratory management team, all sections of the laboratory and Respiratory Therapy
Works with Directors, management team, and quality improvement teams, to coordinate and establish annual quality assurance calendar
Assures all quality improvement and monitoring activities are completed in a timely manner
Develops and proposes, in collaboration with the management team, appropriate improvement projects utilizing statistical process controls, including but not limited to: measurement of customer satisfaction and perception of quality, measurement of cost effectiveness and productivity, and reduction/elimination of non-quality improvement processes and unnecessary redundancies
Facilitates the CQI (Continuous Quality Improvement) and SPC (Statistical Process Control), process in each section of the laboratory
Works with appropriate staff to identify key indicators of service, establish methods for monitoring performance, and to initiate improvement activities
Facilitates the implementation of processes to assure the best quality outcome is delivered to customers/clients in a customer-focused manner
Provides support to the technical and non-technical managers to target, measure, and report quality improvement opportunities

Fulltime

Quality Control Manager

Rowan Digital Infrastructure is looking for a Senior Associate, Quality Control ...

Location

United States , Denver

Salary:

140000.00 - 160000.00 USD / Year

Rowan Digital Infrastructure

Expiration Date

Until further notice

Requirements

Relevant college degree or commensurate relevant experience
Relevant construction experience (3 years minimum) for a decently sized general contractor or owner developer
Previously held site-based QA/QC roles for a minimum of 2 years
Background in Data Center development
Be familiar with large projects or have a history of multiple projects running at the same time
Knowledge of construction worksite safety practices
Proficient in Procore and other construction management software
Working knowledge of green building practices
Excellent communication and collaboration skills
Strong organizational skills

Job Responsibility

Responsible for actively monitoring the quality control program from an owner/developer perspective on all site infrastructure, substation and construction
Ability to plan and lead quality discussions as needed
Work closely with Rowan pre-con, project executive, PM’s, construction, and safety team members
Develop trusting relationships with clients, JHA’s, GC’s, sub-contractors to aid in the successful delivery of the project
Conduct site surveys to ensure work is installed per contract documents and work with PMs to update schedule with quality control inspection activities
Lead closeout efforts as we approach substantial completion to assemble all closeout documents, O&M manuals and warranty, preventive maintenance agreements, -etc.
Provide continuous improvement to the Rowan and our partner QA/QC programs
Actively work in Procore as your primary documentation tool
Read and review client-specific requirements and check for compliance
Lead Weekly PM Lease Compliance Meetings

What we offer

Hybrid working environment
Team building and educational opportunities
Generous benefits package including robust health benefits and a 401(k) company contribution
Unlimited PTO
Competitive compensation and bonus plan

Fulltime

Vice President, Quality

The Vice President, Quality serves a pivotal role in providing quality leadershi...

Location

United States , Verona

Salary:

280000.00 - 340000.00 USD / Year

Arrowhead Pharmaceuticals, Inc

Expiration Date

Until further notice

Requirements

BS in Life Sciences or related discipline
15+ years in QA or compliance with particular experience in cGMP commercial manufacturing environment and with experience in GCP clinical programs for drugs and/or biologics preferred
10+ years in a previous management role
Experience with developing a QMS and hosting successful regulatory agency inspections
Ability to thrive in a fast-paced environment, with experience in sponsor quality oversight responsibilities for contract vendors across all GxP areas
Implementation of internal phase appropriate GMP drug substance manufacturing & testing systems
Prior successful management of a Quality Management System for commercial product
Drug development through commercial manufacturing compliance experience
Excellent oral and written communication skills required
Strong computer skills utilizing a Microsoft environment (e.g. Word, Excel, Access, PowerPoint)

Job Responsibility

Develop and facilitate Quality Systems as delineated in the Quality Manual to support Arrowhead’s clinical development pipeline and preparations for product commercialization
Implement and maintain an overall Quality Management System (QMS) meeting the requirements of activities conducted within Arrowhead
Develop and oversee the internal Quality Control (QC) lab department and operations
Support activities relating to clinical QA GCP regulations at the Pasadena location
Ensure systems are in place for conducting and tracking employee training required by GxP regulations
Support efforts pertaining to internal design, construction, commissioning, and qualification of GMP facilities
Review and approve outsourced contract manufacturing documentation such as validation protocols and reports
master batch records
deviations
analytical methods and methods validation

What we offer

competitive salaries and an excellent benefit package

Fulltime

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Manual QC (Data Testing)

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