Quality Inspection Jobs in Lisbon
Quality Inspection Jobs in Lisbon
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Responsibilities Extraction of test scenarios and subsequent design and execution of both manual and automatedtesting. Design of scenarios to ensure coverage of both positive and negative pathways Work within a BDD framework and design web UI automation tests using selenium within a C More...
Responsibilities Extraction of test scenarios and subsequent design and execution of both manual and automatedtesting. Design of scenarios to ensure coverage of both positive and negative pathways Work within a BDD framework and design web UI automation tests using selenium within a C More...
Responsibilities Extraction of test scenarios and subsequent design and execution of both manual and automatedtesting. Design of scenarios to ensure coverage of both positive and negative pathways Work within a BDD framework and design web UI automation tests using selenium within a C More...
Responsibilities Extraction of test scenarios and subsequent design and execution of both manual and automatedtesting. Design of scenarios to ensure coverage of both positive and negative pathways Work within a BDD framework and design web UI automation tests using selenium within a C More...
Responsibilities Extraction of test scenarios and subsequent design and execution of both manual and automatedtesting. Design of scenarios to ensure coverage of both positive and negative pathways Work within a BDD framework and design web UI automation tests using selenium within a C More...
Responsibilities Extraction of test scenarios and subsequent design and execution of both manual and automatedtesting. Design of scenarios to ensure coverage of both positive and negative pathways Work within a BDD framework and design web UI automation tests using selenium within a C More...
We are seeking a skilled and experienced Senior QA Automation Engineer to join our Technology Center in Portugal. You will join a local team that is part of a wider international development team spanning the US Portugal and India. On this role youll be contributing to the quality ass More...
We are seeking a skilled and experienced Senior QA Automation Engineer to join our Technology Center in Portugal. You will join a local team that is part of a wider international development team spanning the US Portugal and India. On this role youll be contributing to the quality ass More...
We are seeking a skilled and experienced Senior QA Automation Engineer to join our Technology Center in Portugal. You will join a local team that is part of a wider international development team spanning the US Portugal and India. On this role youll be contributing to the quality ass More...
We are seeking a skilled and experienced Senior QA Automation Engineer to join our Technology Center in Portugal. You will join a local team that is part of a wider international development team spanning the US Portugal and India. On this role youll be contributing to the quality ass More...
We are seeking a skilled and experienced Senior QA Automation Engineer to join our Technology Center in Portugal. You will join a local team that is part of a wider international development team spanning the US Portugal and India. On this role youll be contributing to the quality ass More...
We are seeking a skilled and experienced Senior QA Automation Engineer to join our Technology Center in Portugal. You will join a local team that is part of a wider international development team spanning the US Portugal and India. On this role youll be contributing to the quality ass More...
Senior Medical Writer Pharmacovigilance Aggregate Reports- Homebased In Europe
The PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk managemen More...
Senior Medical Writer Pharmacovigilance Aggregate Reports- Homebased In Europe
The PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk managemen More...
Senior Medical Writer Pharmacovigilance Aggregate Reports- Homebased In Europe
The PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk managemen More...
Make an impact by working for sectors where technology is the enabler everything is groundbreaking and theres a constant need to be innovative. Be part of the team that combines business knowledge technological edge and a design experience. Our different backgrounds and knowhow are More...
We are looking for a meticulous Content Moderator to join our team in Lisbon. As a Content Moderator you will be pivotal in upholding content quality and safety on our platform ensuring compliance with guidelines to enhance user satisfaction. Responsibilities: Monitor and moderate use More...
Senior Medical Writer Pharmacovigilance Aggregate Reports- Homebased In Europe
The PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk managemen More...
Senior Medical Writer Pharmacovigilance Aggregate Reports- Homebased In Europe
The PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk managemen More...
Senior Medical Writer Pharmacovigilance Aggregate Reports- Homebased In Europe
The PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety.Key ResponsibilitiesIndependent authoring editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports risk managemen More...
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