Found 5 Switzerland Jobs

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  • £424/day
Have you ever considered a contract role in Switzerland? I am looking for skilled and experienced Software Developers for a contract at a fantastic company based in the city of Geneva. You will be responsible for - Mirgration to a cloud base storage solution - Development of data migration and transformation scripts using Java, Python and SQL. This contract role is full time and will pay up tp €500 for every day that is worked. If you are available and interested please send me your CV and avalibility and a good time to discuss further
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Senior Project Manager/Project Director I have an opportunity for a Senior Project Manager/Project Director on a contract basis for a Pharmaceutical Project in Switzerland. You must have pharma experience through design and delivery. Previous experience on pharmaceutical projects is essential. Accommodation, per diem and travel all included. If this is a role that interests you and you would like further information please email (url removed) or call (phone number removed)
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Clinical Data Manager 95 – 127 CHF/hr Switzerland 12 Month Contract Are you looking for a new and exciting opportunity to put your clinical data management skills and experience to good use? If so, S3 Discovery has the role for you! Our client is looking for a Clinical Data Manager to work within their dedicated and experienced team. The role involves working with Oncology Trials at their site based near Geneva, Switzerland. The role is of high priority, and therefore is on a first come, first serve basis. Are you ready and able to start your next contract role ASAP? Main responsibilities as a Clinical Data Manager include but not limited to: * Define and manage Clinical Data Management timelines on multiple studies or programs for the responsible CROs * Prepare data validation plans, data management plans and other study-specific procedures and guidelines in compliance with standard processes and SOPs * Coordinate data management activities for assigned studies/programs, including eCRF design, EDC system set up, user acceptance testing, users training, database release, data review, and query generation and data coding * Ensure that appropriate study-specific training is provided to assigned study teams and documented * Ensure ongoing and timely data capture and data cleaning, including external data sources * Deliver/coordinate data management support to study teams to support timely and ongoing data review and monitoring * Ensure study timelines are met and data quality is according to high industry standards * Ensure adherence to GCP, regulatory guidelines, standard processes, and SOPs * Transfer, lock and archive databases What skills, experience and qualifications do I need? * Degree level education * At least 5 years’ experience in clinical data management * Experience using major EDC systems (Medidata RAVE) and related tools and technologies * Prior experience leading data management studies, delivering quality databases that meet regulatory requirements * Must be fluent in English * German or French language skills are a bonus How do I apply? The application process for this role is easy. Permitting you match said criteria, simply click and apply to the advert, and if successful, you will be contacted by a member of the team ASAP. Due to the number of applications we receive, if you have not been contacted within 1 week, unfortunately you have not been successful for this role. All successful applications are subject to S3 Discovery’s stringent vetting and security checks. S3 Discovery is proud to be an equal opportunities employer and is committed to creating a diverse environment. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender identity or expression, sexual orientation, national origin, genetics, disability, age or veteran status
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Jocelyn Blackham is recruiting for a Design Quality Engineer to join a company in the Medical Device industry at their site based in Oberdorf on a contract basis until the end of 2020. The main purpose of the role will be to: - Play a key role in the team, focusing on the Life Cycle Management activities - Enhance the Design Control and Risk Management processes to better reflect state of the art practices and drive continuous improvement - Apply statistical methods and process/design excellence tools to establish test plans as well as evaluate test data and processes. Perform Gage R&R studies - Conduct and lead design verification and validation activities - Conduct and lead design / process failure mode effects and analysis - Provide leadership in all areas of the Quality System, including, but not limited to Corrective & Preventive Actions, Complaints, Nonconforming Materials, Risk Management, etc. Further responsibilities will include: - Effective communication at all levels within Quality as well as cross functionally with  departments such as Product Development, Regulatory Affairs, Manufacturing, and Marketing - Sharing knowledge and following all laws and policies that apply to the job, and maintain the highest levels of professionalism, ethics and compliance at all times - Accountability for the successful delivery of multiple simultaneous projects, spanning multiple functional areas and locations In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - A minimum of a Bachelor's degree in Engineering or related technical or scientific discipline with hands on experience in related field is required - Working knowledge of Design Controls, GMPs, QSR, 21 CFR 820, MDD 93/42/EEC,  ISO13485 and ISO14971 quality requirements is required - Experience in a Medical Device regulated environment - Previous Quality Engineering experience is preferred - Development and manufacturing experience is preferred - Fluency in English is required, good knowledge of German would be a strong asset This is an excellent opportunity to join a global medical device company. Please quote reference 47325 in all correspondence
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  • £400 - £500/day
Sybase DBA: As part of the programme to build out an innovation lab we are seeking a Sybase DBA with experience of production support. We are seeking someone with good troubleshooting skills to work in a global database team supporting Sybase/ MS SQL Server database products/ platforms in an enterprise scale environment. As a Sybase DBA your experience and skills will include: * Maintaining and supporting Sybase databases around the globe * Supporting the developers and the application teams. * Proficiency with Sybase DBA tasks as well as with SQL commands to develop stored procedures and triggers * 5 years experience with Linux, SRDF, storage, backup (preferably Commvault), monitoring, auditing and scripting. * 5 years experience with Sybase replication: classic, warm standby and MSA * Sybase installations, upgrades, troubleshooting * Experience Sybase IQ is an advantage * Wide experience with Sybase performance tuning * Experience of MS SQL Server Versions (Apply online only) is an advantage * Full understanding of RFS, Incident and change management service delivery principles ITIL * Commercial experience in a production environment We are looking for a Sybase DBA who will: * Design and implement complex changes * Troubleshoot and solve incidents * Monitor and analyze Sybase performance issues * Work with numerous technical teams to improve core infrastructure
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