Job Description The QA Specialist is responsible for the accuracy and completeness of the ICT solution by verifying technical and/or functional requirements. The core responsibilities of the role include: identifying the types of tests to be performed
About the job Are you eager to take a new opportunity? Are you looking for a challenging and dynamic environment where to build your professional career? Description We are looking for a Process Audit to join
I am looking for a motivated Quality Manager to join my clients team at their Parma office . The successful candidate will contribute to the continuous development of our management system, ensuring compliance with international standards
About usChiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular
Role : Senior QA Automation Engineer (Remote) Location : Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking a Senior QA Automation Engineer to design, implement, and maintain automated testing frameworks for
The QA Specialist is responsible for the accuracy and completeness of the ICT solution by verifying technical and/or functional requirements. The core responsibilities of the role include: identifying the types of tests to be performed (units, integration,
Chiesi is seeking a Senior GDP QA Specialist to strengthen the GDP Quality Management System in a dynamic pharmaceutical environment. You will own core GDP QA activities, autonomously manage deviations, CAPA, change control, audits, and temperature excursions, and
QUINEL LTD is seeking a candidate to join the online gaming assessment team for functional and compliance testing of gaming systems. The role is onsite, with a structured training and qualification path before independent work. Candidates must
Specialista QA Validation - Supporto Attività di Review Tipo di Impiego: Full Time Descrizione del ruolo: La risorsa sarà inserita nel team QA Validation con il compito di supportare le attività di review e pre-approvazione delle modifiche (change)
About usChiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular
About usChiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular
Overview In this role you will safeguard pharmacovigilance quality across corporate and affiliate levels, ensuring compliance with regulations and internal standards. You will drive deviations management, CAPA, and change control within the PV QMS, collaborating with
Part of the MoOngy Group, Agap2 operates across the European market in 14 countries, providing engineering and plant consultancy services. Since 2018, Agap2 Italia has been operating nationwide in the following sectors: Energy, Oil & Gas,
About Us ProductLife Group (PLG) is a dedicated life sciences and pharmaceutical outsourcing and consulting company providing expertise and services in areas such as Product Development, Market & Patient Access, Regulatory Affairs and Safety & Vigilance
Select how often (in days) to receive an alert: About Phibro Animal Health Corporation Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer
Specific activities and responsibilities: Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment Preparation of validation protocols, reports and related documentation. knowledge of GMP regulations Ensure compliance with GMP requirements and internal
Datacolor, a global leader in color management solutions, provides software, instruments and services to improve the precision, performance and efficiency of your color workflow. We understand that details matter, and precise, consistent replication is essential. For
A prestigious company operating in the Pharma / Life Sciences sector has entrusted us with the search for a: PART-TIME CONTRACT DURATION: 18–24 months START DATE: May 2026 Do you have experience managing complex changes in
Specific activities and responsibilities: Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment Preparation of validation protocols, reports and related documentation. knowledge of GMP regulations Ensure compliance with GMP requirements and internal
Specific activities and responsibilities: Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment Preparation of validation protocols, reports and related documentation. knowledge of GMP regulations Ensure compliance with GMP requirements and internal