QA / QC Engineer Job at ASSYSTEM (Honnavar)

Senior QA Engineer

VarSome.com is the world’s leading website for professional human genetics. VarS...

Location

Poland

Salary:

Not provided

Saphetor

Expiration Date

Until further notice

Requirements

BSc and/or MSc Degree in Computer Science, Engineering, or other STEM degrees
At least 4 + years of experience in Quality Assurance, focusing on test automation, including designing, implementing, and maintaining test frameworks and test cases
Familiarity with test management/documentation tools (e.g., TestRail, QC)
Working knowledge of API testing tools (e.g., Postman, SoapUI)
Hands-on experience with Selenium WebDriver and test frameworks such as Pytest
Programming experience with Python
Strong analytical skills, attention to detail, and ability to work independently as well as in a team
Fluency in English (written and spoken)
Be a flexible team player and have the ability to manage a project
Highly motivated and detail-oriented individual

Job Responsibility

Conduct automation and manual testing, while documenting test methodologies
Gain in-depth knowledge of our clinical platform, which enables fast and accurate variant detection, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels to give the highest quality to our customers
Participate in the full product development life-cycle: defining test requirements at the start of a project, tracking and managing test issues, ensuring that the software meets its acceptance criteria, signing off on releases for quality purposes and reviewing test documentation
Continue to develop our automation suite and embed this within our development process
Write concise documentation and revise older test cases to achieve greater testing coverage
Develop new testing frameworks where necessary
Mentor junior QA engineers and promote best testing practices across the team

What we offer

A position in a fascinating healthcare growth domain, at the cutting edge of technology
A competitive compensation package
Remote work with occasional meetings
Endless learning opportunities while transferring new technologies from academics to clinical practice all over the world

Fulltime

Senior QA Engineer

VarSome.com is the world’s leading website for professional human genetics. VarS...

Location

Romania

Salary:

Not provided

Saphetor

Expiration Date

Until further notice

Requirements

BSc and/or MSc Degree in Computer Science, Engineering, or other STEM degrees
At least 4 + years of experience in Quality Assurance, focusing on test automation, including designing, implementing, and maintaining test frameworks and test cases
Familiarity with test management/documentation tools (e.g., TestRail, QC)
Working knowledge of API testing tools (e.g., Postman, SoapUI)
Hands-on experience with Selenium WebDriver and test frameworks such as Pytest
Programming experience with Python
Strong analytical skills, attention to detail, and ability to work independently as well as in a team
Fluency in English (written and spoken)
Be a flexible team player and have the ability to manage a project
Highly motivated and detail-oriented individual

Job Responsibility

Conduct automation and manual testing, while documenting test methodologies
Gain in-depth knowledge of our clinical platform, which enables fast and accurate variant detection, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels to give the highest quality to our customers
Participate in the full product development life-cycle: defining test requirements at the start of a project, tracking and managing test issues, ensuring that the software meets its acceptance criteria, signing off on releases for quality purposes and reviewing test documentation
Continue to develop our automation suite and embed this within our development process
Write concise documentation and revise older test cases to achieve greater testing coverage
Develop new testing frameworks where necessary
Mentor junior QA engineers and promote best testing practices across the team

What we offer

A position in a fascinating healthcare growth domain, at the cutting edge of technology
A competitive compensation package
Remote work with occasional meetings
Endless learning opportunities while transferring new technologies from academics to clinical practice all over the world

Fulltime

Senior QA Engineer

VarSome.com is the world’s leading website for professional human genetics. With...

Location

Greece , Athens

Salary:

Not provided

Saphetor

Expiration Date

Until further notice

Requirements

BSc and/or MSc Degree in Computer Science, Engineering, or other STEM degrees
At least 4 + years of experience in Quality Assurance, focusing on test automation, including designing, implementing, and maintaining test frameworks and test cases
Familiarity with test management/documentation tools (e.g., TestRail, QC)
Working knowledge of API testing tools (e.g., Postman, SoapUI)
Hands-on experience with Selenium WebDriver and test frameworks such as Pytest
Programming experience with Python
Strong analytical skills, attention to detail, and ability to work independently as well as in a team
Fluency in English (written and spoken)
Be a flexible team player and have the ability to manage a project
Highly motivated and detail-oriented individual

Job Responsibility

Conduct automation and manual testing, while documenting test methodologies
Gain in-depth knowledge of our clinical platform, which enables fast and accurate variant detection, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels to give the highest quality to our customers
Participate in the full product development life-cycle: defining test requirements at the start of a project, tracking and managing test issues, ensuring that the software meets its acceptance criteria, signing off on releases for quality purposes and reviewing test documentation
Continue to develop our automation suite and embed this within our development process
Write concise documentation and revise older test cases to achieve greater testing coverage
Develop new testing frameworks where necessary
Mentor junior QA engineers and promote best testing practices across the team

What we offer

A competitive compensation package combined with additional benefits
Endless learning opportunities, while transferring new technologies from academics to clinical practice all over the world

Fulltime

Qa/qc tester

The Marcus Evans Group, founded in 1983, is a global Business Intelligence and E...

Location

India , Mumbai; Kerala; Hyderabad

Salary:

Not provided

Evan Marcus

Expiration Date

Until further notice

Requirements

Bachelor's degree in computer science, Engineering or related field
Strong proficiency in programming languages (e.g., Python, Java, C#) for test automation
Solid understanding of QA/QC methodologies and best practices
Strong communication and documentation skills and the ability to collaborate effectively with cross-functional teams
1-2 years of experience in a similar role within a software development/IT environment
Strong knowledge of QA methodologies, software testing lifecycle, and defect lifecycle
Proficient with test management and defect tracking tools (e.g., JIRA)
Experience working in Agile/Scrum environments
Familiarity with JUnit testing framework or other frameworks
Excellent analytical thinking and problem-solving abilities

Job Responsibility

Develop and execute comprehensive test plans, test cases, and test scripts based on technical and business requirements
Perform both manual and automated testing to validate product functionality, usability, and performance
Log and track issues using defect tracking tools such as JIRA, ensuring timely resolution
Collaborate with developers, product managers, and operations teams to resolve bugs and ensure high-quality releases
Conduct root cause analysis for recurring issues and contribute to process improvements
Review technical and functional documentation for clarity and completeness
Participate in requirement analysis and provide QA input during sprint planning and design
Communicate testing progress, results, and issues effectively to cross-functional teams and management
Prepare quality metrics, dashboards, and testing reports for key stakeholders

What we offer

Competitive base salary
Part of a highly skilled and collaborative team
Bonus available on performance

Validation Engineer Medior

We are seeking a highly skilled Validation Engineer to join our pharmaceutical m...

Location

Belgium , Wavre

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Bachelor's degree in Pharmaceutical Sciences, Chemical Engineering, Biotechnology, or related field
5+ years of validation experience in pharmaceutical manufacturing
Experience with sterile manufacturing and biologics is highly preferred
Knowledge of Belgian pharmaceutical regulations and EU GMP
Strong understanding of validation lifecycle approaches
Proficiency in risk-based validation methodologies (ICH Q9)
Experience with continuous manufacturing validation (ICH Q13)
Knowledge of data integrity requirements in regulated environments
EU GMP (especially Annex 15 - Qualification and Validation)
ICH Guidelines (Q8, Q9, Q10, Q11, Q12, Q13)

Job Responsibility

Lead and execute process validation activities for new and existing pharmaceutical products
Develop and implement validation master plans and validation protocols (IQ/OQ/PQ)
Ensure validation activities align with ICH Q8/Q9/Q10 guidelines
Conduct risk assessments using ICH Q9 principles for validation strategies
Perform qualification activities for manufacturing equipment, utilities, and systems
Execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ)
Manage re-qualification activities per regulatory requirements
Coordinate with suppliers for Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT)
Ensure all validation activities comply with EU GMP Annex 15 and Belgian regulatory requirements
Prepare and review validation documentation for regulatory submissions

What we offer

Rapid growth: Amaris has doubled its workforce in Belgium in two years, providing numerous growth opportunities for employees
Prestigious projects: Candidates will work with renowned clients in the pharmaceutical, biotechnology, and European institutions sectors on impactful missions
International environment: An agile and dynamic structure promotes intrapreneurship and meritocracy, with international exposure at the heart of Europe

Fulltime

Quality Manager

If you’re looking for a career with a company that has a ‘Can Do’ attitude, then...

Location

Australia

Salary:

Not provided

Primero Group

Expiration Date

Until further notice

Requirements

Minimum 8–10 years of multi-discipline experience within a contractor environment
Proven experience managing, leading, and supervising teams of 4–6 personnel
Relevant experience in project QA/QC environments (engineering, construction, or EPC projects)
Strong communication, leadership, and stakeholder management skills
Ability to work in a fast-paced project delivery environment
Current driver’s licence and ability to meet site medical and safety requirements

What we offer

Competitive Compensation
Contemporary Rostering
Flexible Working Arrangements
Career Opportunities
Paid Parental Leave
Health and Wellbeing Support
Benefits & Discounts
Employee Referral Rewards
Onsite Gym (remove for site-based roles)

Fulltime

Senior Specialist Quality

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of quality compliance experience
Master’s degree and 4 years of quality compliance experience
Bachelor’s degree and 6 years of quality compliance experience
Associate’s degree and 10 years of quality compliance experience
High school diploma / GED and 12 years of quality compliance experience
Background in Quality, QC, QA, Engineering desirable
Understand quality documentation and laboratory practices including general methodologies, specifications and product quality standards
Excellent communication skills for both internal conversations and when representing Amgen at external forums
Conflict resolution
Teamwork and Networking

Job Responsibility

Lead project management of major global pharmacopoeias (USP, Ph. Eur., JP, ChP), ensuring structured review and implementation of periodic updates
Coordinate cross-functional teams and site points of contact at global manufacturing sites to execute required changes in alignment with compliance timelines
Ensure all pharmacopeial changes are appropriately assessed, documented, tracked, and maintained in a current state within Amgen systems
Author compendial assessments within Amgen’s documentation management systems for audit readiness purposes
Proactively monitor early signals, emerging trends, and evolving regulatory issues impacting global operations as it relates to pharmacopoeia matters
Represent Amgen’s approved positions in external organizations and trade associations as assigned, to influence and shape pharmacopeial public standards
Liaise with regulators through industry associations, supporting advocacy and alignment efforts
Partner with internal SMEs to ensure scientific alignment on pharmacopeial developments and regulatory changes
Support knowledge-sharing across functions to enhance understanding of external landscape developments
Provide back-up support within External Affairs as needed to ensure business continuity

What we offer

A 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
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Qa / Qc Engineer

M//s HPPL developing the Barge Berth at Honnvar Karnataka. As part of developmen...

Location

India , Honnavar

Salary:

Not provided

ASSYSTEM

Expiration Date

Until further notice

Requirements

B.E (Civil) with minimum 5 to 10 years experience in Marine construction work like Jetty/wharf and associated structures

Job Responsibility

Assisting the Resident Project Manager in the following activities: Overall Project Management Control
Preparing the RFI and BBU etc
Construction Supervision
Quality Control and Quality Assurance of various components that are being implemented
Certifying Bill of Measurements for Interim Payments

QA / QC Engineer

ASSYSTEM

Location:
India , Honnavar

Category:
Construction

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 09, 2026

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