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269 ofert pracy dla: Qualified Person Job

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  • competencies? Do you really want to be a essential part of the company? Do you want to make a contribution to the implementation of and maintaining an efficient (c)GMP quality system for biotechnological products? Then this is the job for you! RESPONSIBILITIES You will

  • world and has in recent years a significant growth. ROLE DESCRIPTION In this job you will be responsible for the supervision, without any interference of third persons, of the business processes of pharmacy, related to the drug manufacturing

  • pharmaceutical industry and in GMP environment. Experience with “Change controls” and “Deviations”. - Eligible to become approved as Qualified Person, meaning you are knowledgeable of and skilled to fulfil the requirements of EU directive 2001/83/EC article 49 (Qualified Person) and/or GDP guidelines 2013/C

  • this role you will be Qualified Person for Pharmaceutical Supply Chain RESPONSIBILITIES - Batch release within the European Union (EU) of medicinal products for human or veterinary use or made for export. - Checking of the manufacture and testing of the batch in

  • In this role you will be Qualified Person for Pharmaceutical Supply Chain RESPONSIBILITIES - Batch release within the European Union (EU) of medicinal products for human or veterinary use or made for export. - Checking of the manufacture and testing of the

  • van uw supply chain kan behandelen. ROLE DESCRIPTION Wil jij als Qualified person aan de slag net over de grens in het mooie België? Ben jij er klaar voor om de kwaliteit te waarborgen van elke batch die geproduceerd is? Jij zal als

  • and GMP compliance RESPONSIBILITIES - Support Qualified Person - Ensure GMP is respected due to production and packaging - Asses Products released by other Qualified Person for distribution in Europe - Review batch documents - Negotiate Quality Agreements ...

  • ROLE DESCRIPTION You will be responsible for supporting the Qualified Person and act as the back-up QP. Most of all you are responsible for batch reviews and related activities. The duration of the project will be around 3 months with a good change on an extension ...

  • DESCRIPTION Het is jouw taak als Qualified Person om zorg te dragen voor de vrijgifte van verhandelde goederen. RESPONSIBILITIES Je draagt de verantwoording voor het kwaliteitssysteem en het volgen/naleven van GMP, GDP en ISO richtlijnen. Verder

  • international Quality organization - Responsible for ensuring consistency and communication within Quality department and with key stakeholders REQUIREMENTS - Registered Qualified Person - GMP GDP experience - Fluent both in Dutch & English - At least 8 years of

  • SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...

  • SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...

  • SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...

  • SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced ...

  • the clients facility to ensure adequate, effective and efficient use of the Quality system, programs and procedures. Moreover, some members of the Clinical Quality team act as a Qualified Person. They release Investigational Medicinal products used in EU clinical studies, manage Quality Agreements

  • The Clinical QA team has QA oversight for all clinical products received, released and distributed from the clients facility to ensure adequate, effective and efficient use of the Quality system, programs and procedures. Moreover, some members of the Clinical Quality team act as a Qualified Person

  • Junior Web Developer - Krakow We're looking for developers to join our growing team and help us build great products while contributing to our community with open source, writing, events, and more. Job Summary We’re an events company, coordinating events throughout the UK and Australia as

  • deviations, CAPAs, complaints and validations are performed correctly. REQUIREMENTS - Msc degree in pharmaceutical industry - Registered as Qualified Person (QP) and experience in pharma release - Knowledge and experience in the field of GMP, GDP, pharmaceutical - You

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