Gamp Jobs in Luxembourg
Gamp Jobs in Luxembourg
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About the Job Oleson specialises in delivering highquality talent and solutions that enhance the capabilities and operational excellence of our global customers. We are focused on matching the dynamic needs of Data Centre and Life Science clients with skilled professionals thereby d More...
Computer Systems Validation Consultant
The CSV Consultant will develop and maintain comprehensive validation plans, prepare validation documentation including user requirements and test scripts, conduct and oversee installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) tests, an More...
Job Title: CSV Lead Location: Raritan NJ Onsite Duration / Term: 6 months Contract Job Description: Validating ERP to AWS Data migration process and Validating Data migration project Experience in the Pharmaceutical biotechnology or medical device industry 5 years experienc More...
Overview: Tekwissen Group is a workforce management provider throughout the USA and many other countries in the world. This client is a German multinational Pharmaceutical and biotechnology company and one of the largest pharmaceutical companies in the world headquartered in More...
Perform project electrical and pneumatics hardware and PLC/HMI software design including test and validation activities on equipment and systems in accordance with applicable regulatory standards and to cGMP and GAMP 5 guidelines for the pharmaceutical industry. Liaise with associa More...
CQV Equipment validation consultant Boston MA OR Rhode Island(Onsite) 3 Months Contract I have an opening in Boston for a CQV Equipment validation consultant. It is onsite for the first 3 months maybe longer in Boston but also may have work to be done in Rhode Island. They want som More...
r du en erfaren QA inom Life Science med fokus p kvalitetsskring av datoriserade system eller r du redan en etablerad QA ITkonsult inom branschen Har du byggt upp en gedigen erfarenhet och knner att du r redo att ta nsta steg in i en senior konsultroll p en av Sveriges mest eftertrakt More...
Title: CQV Process Support Engineer Location: Holly Springs NC Onsite Key Responsibilities Provide CQV process support to clients that manufacture GMP products. Develop CQV planning doents to manage CQV projects. Generate and execute CQV protocols using Good Doentation Practices ( More...
Using initiative and a self-driven approach to identify and deliver continuous improvement opportunities, the lead will be encouraged to: Ensure that all IT systems used by sites remain compliant throughout their lifecycle, with the relevant compliance policies, standards and More...
We are looking for curious and experienced colleagues seeking the opportunity to join a fantastic company where we together have the aspiration of becoming best in class within Automation Solutions for Pharmaceutical Engineering.The Process Automation teamwork with consultancy design More...
CK Group are recruiting for an experienced Senior Validation Specialist to join a growing Cell Therapy CDMO to be based at their site in Cambridge, on a permanent basis. This role will be fully onsite. The Role: Reporting to the Validation Manager, you will support multiple p More...
About Company: Our Company is a global technology consulting and digital solutions company that enables enterprises to reimagine business models and accelerate innovation through digital technologies. Powered by more than 84000 entrepreneurial professionals across more than 30 countri More...
Hi Hope you are doing well! Please find the below job description & please share your updated resume. Role: CSV Lead Location: Raritan NJ Hybrid(23 days a week onsite) Duration: Long term Job description: Experience Validating ERP to AWS Data migration process and Validating Data More...
Qui sommes nous Cr en 2009 est bas sur le partage et lactionnariat : 100% de nos actionnaires sont salaris.Aujourdhui prsent linternational avec 2500 collaborateurs nous nous engageons maintenir une performance industrielle et conomique au travers un haut niveau dexpertise (4 delive More...
We need local candidates only Location Raritan NJ(Hybrid) Job Description (Posting). Computer System Validation In addition to validation and regulation experience the resource should have the following experience: 37 years of relevant experience; can work independently a More...
Qui sommes nous Cr en 2009 est bas sur le partage et lactionnariat : 100% de nos actionnaires sont salaris.Aujourdhui prsent linternational avec 2500 collaborateurs nous nous engageons maintenir une performance industrielle et conomique au travers un haut niveau dexpertise (4 delive More...
Accountabilities: As a Senior IT Quality Manager, you will use your pharmaceutical regulatory compliance experience and intelligence to support and deliver an integrated IT QM strategy. You will be responsible for understanding and applying regulatory compliance policies and st More...
Would you like to join a leading Digital Solution Company and contribute to innovative solutions that are built on a daily basisOur client is a leading global provider of IT solutions and services known for their customercentric approach to digital transformation. With a rich history More...
Validation Specialist With Clinical Development And Supply Chain Drug Discovery
Hi Hope you are doing well! Please find the below job description & please share your updated resume. Role: Validation specialist Location: Raritan NJ Hybrid Duration: Long term Job Details: 10 years experience in Computer System Validation or Quality management or Business Analys More...
Validation Engineer Location:TucsonAZ (100% onsite) Duration:12 months extendable The Validation Engineer will be responsible to ensure that validation requirements are met for all existing and new equipment/ facilities/utilities and processes by preparing and executing detailed val More...
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