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Lead Civil and Structural Engineer – 12 Month Contract - CAPEX Biotech Project - Switzerland   I am collaborating one of the biggest CDMO in Europe that is now undertaking a CAPEX Project in Switzerland and is looking for a Lead Structural Engineer to take on responsibilities from design to handover.   Due to being at an early stage of the project for a secondary manufacturing site they are looking to expand their team of consultants with a Lead Civil and Structural Engineer that is interested in expanding his/hers area of expertise within the Biotech or who is already experienced in the industry and might be just looking for a new challenge in Switzerland.   Requirements: Completed degree in Civil Engineering or Architecture A minimum of 10 years of work experience with considerably working experience within the Life Science Industries or Chemical Experience working on “multidisciplinary landscape projects” covering all aspects Experience in  project planning and implementation of interdisciplinary projects Experience in leading and managing any external partners in the delivery of the project scope across different phases from design through to Handover, Fluency in German and English is Mandatory.  Responsibilities: Development and planning of construction projects in close cooperation with customers and with interdisciplinary planning teams Lead internal and external planning teams Advising and supporting the client in construction-related matters Ensuring the required qualitative and quantitative construction resources Monitor the costs, deadlines and quality of the construction projects that you oversee  The length of the contract will be 12 months with possibility of extension and we are looking at an immediate start date. Experience in within the EU is needed. Please note we can only accept applications from candidates who hold valid European Union passport and are able to work in Europe without visa sponsorship. For a confidential discussion about quality assurance, engineering and project management roles, then send your CV to (url removed) or call me, Elena Cazacu, Senior Recruitment Consultant for Switzerland at (phone number removed). Established in 1978, NES Global Talent provides a complete range of contract and permanent talent solutions to the Oil and Gas, Power, Construction and Infrastructure, Life Sciences, Manufacturing and IT sectors worldwide. With more than 40 offices in 28 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. Offering far more than a traditional recruitment service, we fully support our contractors while they are on assignment with everything from securing visas and work permits, to providing market leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients
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  • £72 - £117/hour Rate neg dependant on location/exp
Role: CQV Engineers Location: Mainland Europe & Ireland Rates: €80.00 p/h - €130.00 p/h dependamt on experience and location Start Date: ASAP I am looking for a number of CQV Engineers for multiple locations in Europe and Ireland including Belgium, Switzerland, Sweden, Holland and Germany. For the Swiss roles I do need candidates who speak French, for all other roles English speakers would be great! I have immediate starts available and I am also looking for phased starters through July and August. I'd be particularly keen to hear from people who are already based in the countries listed above to negate the need for any local quarantine laws still in place. Skill sets I am looking for include Sterile fill finish lines, packaging, VHP Isolator suites, clean utilities, and other equipment / processes associated with Biotech manufacturing. If you are currently actively looking for a new contract or your contract is coming to an end in the next 6 - 8 weeks and you have the skills and experience for these roles then please get in contact with Dave Cattell at ContractArm
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Zenith Technologies are currently looking to hire IT Laboratory Systems Engineer to work with our global pharmaceutical client on NetLab project. Your role will be to provide end user support, administration, installation and issue resolution for laboratory equipment, servers, desktops and software packages. You will perform laboratory upgrades, create system documentation , author and execute test scripts as required. Responsibilities: * Create the development environment e.g. request servers, database, open ports between network layers, configuring windows permissions, connect instruments * Create URS/FRA/FS/CS for Technology Layer * Create the IQ/OQ script * Ensure complete end to end traceability for the documents is built * Create the software package (REALM) that can be packaged to other sites showing interest in installing the system * Troubleshoot and resolve laboratory technical issues involving software, OS, hardware, network, or scientific equipment setup/interfaces. * Perform laboratory equipment, hardware and software upgrades following corporate computer system validation policy and GMP best practices. * Coordinate with users and vendors to facilitate timely resolution of software / hardware issues. * Execute routine system administration and maintenance activities as required. * Create and/or execute software validation scripts to support laboratory. * Create and maintain system documentation including system design specifications, user requirements, functional requirements or routine controlled application change forms. * Proactively communicate with laboratory stakeholders and update helpdesk tracking software as necessary. * Ensure proper user management process is adhered to for all computerised systems * Administer lab system access requests Requirements: * Graduate degree in Engineering, Computer Science, or the Life Sciences * At least 3 years’ experience providing Lab IT systems solutions and support to manufacturing organisations in the biotechnology or pharmaceutical industries. * Excellent communication skills (written and oral). * Strong technical aptitude (i.e. able to read and comprehend technical documentation and execute procedures) *Further details on role available to short listed candidates **Shortlisted applicants who fit the requirements outlined above will be contacted for screen call before being presented to Engineering Management and / or client for technical consideration Zenith Technologies, now a Cognizant Company is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimised to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures and services. Operating across 5 continents and with over 850 skilled employees, Zenith partners with the leading Life Sciences companies globally to provide performance improvements, reduced costs and improve time to market
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  • £108 - £112/hour
Role: Lead CQV Engineers (French Speaking) Location: Geneva Duration: 12 Month Contract Rates: €120.00 p/h My client is a Global Engineering Consultancy supporting Pharma and Biotech projects around the world. They have been awarded a contract for a major Pharma manufacturing company based just outside of Geneva which has just received funding for a major site expansion for their clinical manufacturing facility, and are now looking for Lead CQV Engineers for the project. Suitable candidates should have demonstrable experience leading CQV activities on a sterile or Biotech manufacturing facility including clean utilities, WFI systems and single use delivery systems. For the lead roles, a comprehensive understanding of French language (written, speaking and reading) is required and ideally (but not essentially) you will have worked or contracted in France or Switzerland before. As the project ramps up we will be looking for more skillsets associated with the above project which may not require the same level of language skills (Project Lead, Automation SME, Process Engineers) so please feel free to contact me if you have experience working in the Biotech / Pharma industry and would like the opportunity to live and work in Switzerland. To register your interest in the above role please contact Dave Cattell at ContractArm or apply below
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Regulatory Affairs Expert The company I am delighted to work with a global industry leading nutritional health company. They offer a dynamic and fast paced environment in which to gain further experience and personal growth. About the role * This is a long term ongoing interim contractor position. * The role can be based remotely anywhere in Switzerland and possibly Germany. Travel will be required within these regions. The role is ideal for someone who has strong demonstrable experience in a previous regulatory affairs role. Applicants must have brilliant communication and the ability to work in a multidisciplinary fast paced team. Candidates with minimum 2 years+ in a senior regulatory affairs role, ideally in Switzerland, will be considered. Ongoing training will be provided where necessary. Key responsibilities * Regulatory operational and strategic tasks as required * Communication with business partners, necessary authorities * Global regulatory reporting * Creation and processing of packaging in collaboration with packaging department Required experience; * Bachelor’s degree (or equivalent) in Science preferred * Minimum 2 years + in a similar role * Swiss work experience is highly preferred * All applicants must have strong experience with operational regulatory affairs * Trustworthy personality with solutions-oriented approach * Strong communication and interpersonal skills Keywords: Regulatory affairs, RA, ISO, SOP, senior, expert, contractor, interim, contract, FTC, Switzerland, swiss, Germany, national, global, officer, lead, associate. Harris Lord is acting as a recruitment agency for this role
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