2 jobs found in basel stadt

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    • basel, basel-stadt
    • contract
    For one of our client, a big pharmaceutical company in Basel, we are looking for a Quality Assurance Assistant, to start in August at the latest, for a contract until december 2022.Background:IMP Quality Operations Switzerland is responsible delivering Investigational Medicinal Products “IMPs” to our patients in compliance with cGMP. We are the Quality Partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality and Compliance oversight of all.Our purpose is to create a space for experimentation by coaching and celebrating learnings in order to build a purpose driven quality community that delivers innovative medicines to patients.General Information:• Start Date: ASAP• Latest Start Date: 01.08.2021• End Date: 31.12.2022• Extension: possible• Location: Basel• Worload: 80 - 100%• Remote/Home Office: no, currently due to Corona possibleTasks and Responsibilities:• Reviews Batch Records of Drug Substance and Drug Product and interacts with the corresponding departments• Supports the Quality Assurance manager in daily tasks and RP Delegate for the IMP product release• Reviews Cleaning Assessment Protocols and Reports• Gives GMP compliance input to our stakeholders• Reviews Deviations and ChangesQualifications and Requirements:• Min. Bachelor degree in Life Sciences (e.g. Pharmacy, Chemistry, Biology) (*****)• Min. 3 – 5 years of experience in the pharmaceutical industry, preferred in the GMP environment (*****)• Good knowledge of cGMP and Quality requirements (*****)• Demonstrated experience in manufacturing of Small Molecules is a plus (***)• Ability to communicate clearly and professionally both verbally and in writing in German and in English is a MUST (**)• Good EDV- experience/IT-Flair and experience with MS Office is a plusPersonal Requirements:• Flexible and innovative• Very good communication skills• Ability to communicate clearly• TeamplayerWorking hours:• Flexible working hours, no home office after Corona
    For one of our client, a big pharmaceutical company in Basel, we are looking for a Quality Assurance Assistant, to start in August at the latest, for a contract until december 2022.Background:IMP Quality Operations Switzerland is responsible delivering Investigational Medicinal Products “IMPs” to our patients in compliance with cGMP. We are the Quality Partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality and Compliance oversight of all.Our purpose is to create a space for experimentation by coaching and celebrating learnings in order to build a purpose driven quality community that delivers innovative medicines to patients.General Information:• Start Date: ASAP• Latest Start Date: 01.08.2021• End Date: 31.12.2022• Extension: possible• Location: Basel• Worload: 80 - 100%• Remote/Home Office: no, currently due to Corona possibleTasks and Responsibilities:• Reviews Batch Records of Drug Substance and Drug Product and interacts with the corresponding departments• Supports the Quality Assurance manager in daily tasks and RP Delegate for the IMP product release• Reviews Cleaning Assessment Protocols and Reports• Gives GMP compliance input to our stakeholders• Reviews Deviations and ChangesQualifications and Requirements:• Min. Bachelor degree in Life Sciences (e.g. Pharmacy, Chemistry, Biology) (*****)• Min. 3 – 5 years of experience in the pharmaceutical industry, preferred in the GMP environment (*****)• Good knowledge of cGMP and Quality requirements (*****)• Demonstrated experience in manufacturing of Small Molecules is a plus (***)• Ability to communicate clearly and professionally both verbally and in writing in German and in English is a MUST (**)• Good EDV- experience/IT-Flair and experience with MS Office is a plusPersonal Requirements:• Flexible and innovative• Very good communication skills• Ability to communicate clearly• TeamplayerWorking hours:• Flexible working hours, no home office after Corona
    • basel, basel-stadt
    • contract
    Our client, a biotech company in Solothurn area is looking for a Quality Assurance IIIstart:asapcontract until 31.08.2021 with possibility of extensionDescription:Responsible for Quality oversight to review and approval of validation and engineering life cycle documents (URS, FS, RTM, RA, DS, configuration spec, drawings etc), test protocols, CAPAs, deviations, change controls, work orders and any technical documentation in the scope of Facilities, utilities, equipment and client Execution System (global and local computerized systems) to enable start up, commissioning and qualification of new Large Scale Manufacturing facility. Furthermore advice the project groups as appropriate and be an active member of the groups where the quality input is needed.Skills:more than 4 years experience in quality assurance in pharma or biotech environmentMSc in Life Science or EngineeringAbility to cooperate with people at every level of the organisation and from multiple functions, including engineering, automation, validation, Manufacturing personnel, SME’s on equipment and knowledge of biotechnology API production.Good communication skills in English, verbally and written.Experience with Capa and Change ControlExperience of the validation of laboratory, production equipment and knowledge of production methodology involved in biopharmaceutical drug substance production.Open-mind and ability to value input from colleagues and peers. Able to drive discussion to solve problems with cross functional teams. 
    Our client, a biotech company in Solothurn area is looking for a Quality Assurance IIIstart:asapcontract until 31.08.2021 with possibility of extensionDescription:Responsible for Quality oversight to review and approval of validation and engineering life cycle documents (URS, FS, RTM, RA, DS, configuration spec, drawings etc), test protocols, CAPAs, deviations, change controls, work orders and any technical documentation in the scope of Facilities, utilities, equipment and client Execution System (global and local computerized systems) to enable start up, commissioning and qualification of new Large Scale Manufacturing facility. Furthermore advice the project groups as appropriate and be an active member of the groups where the quality input is needed.Skills:more than 4 years experience in quality assurance in pharma or biotech environmentMSc in Life Science or EngineeringAbility to cooperate with people at every level of the organisation and from multiple functions, including engineering, automation, validation, Manufacturing personnel, SME’s on equipment and knowledge of biotechnology API production.Good communication skills in English, verbally and written.Experience with Capa and Change ControlExperience of the validation of laboratory, production equipment and knowledge of production methodology involved in biopharmaceutical drug substance production.Open-mind and ability to value input from colleagues and peers. Able to drive discussion to solve problems with cross functional teams. 

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