19.05.25 | Vollzeit | Neuchâtel | RandstadOf industry specific compliancestandards/regulations to assays life cycle managementactivities - Participate todaily activities upon request (provide technical and statisticalsupport) Yourprofile • University or engineering degree inmicrobiology - Experience in GMPlaboratory activities - Experience
Später ansehen21.05.25 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Project Plant Engineer. The successful candidate will act as a technical expert, supporting the delivery of projects across site operations. You will coordinate various engineering work packages and serve as the primary contact for technical aspects of assigned installations, including critical GMP
Später ansehen21.05.25 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Engineering Work packages deliver according to the project schedule - Actively challenge over engineered design solutions - Check and approve design deliverables - Be responsible for the Scope, Risk, Stakeholder management of his WS; - Fill his effetely work contribution real contribution according
Später ansehen03.05.25 | Vollzeit | Neuchâtel | CK GroupCK QLS are looking for an experienced engineer, with background in MBR design, ideally for the life sciences industry. You will be joining a Global Pharmaceutical company, based in Neuchatel. Duration Until 19th December 2025, possibility for an extension. Home office 1 day home office a week
Später ansehen12.05.25 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 We are looking for a versatile RF Electronics Engineer to contribute to the development of advanced electronic products. The role involves sub-system requirements definition, designing hardware with associated analysis and ensuring rigorous validation, with a strong emphasis on metrology, PCB
Später ansehen12.05.25 | Vollzeit | Boudry | JobLeads GmbH | CHF 80’000 - CHF 100’000 Integrity and ethics. 7. Provide support and make connections between IT and OT. 8. Act within compliance and legal requirements as well as within company guidelines. Qualifications 1. Engineering educational background in Automation, OT or/and IT. 2. 7+ years of experience in managing pharmaceutical
Später ansehen12.05.25 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Users and manage training toolkits. 5. Participate in audits and continuous improvement initiatives. What you bring to Takeda 1. Degree in life sciences (biotechnology, (bio)chemistry, engineering); advanced degree preferred. 2. 5+ years of experience, with at least 3 years in cGMP manufacturing. 3
Später ansehen02.04.25 | Vollzeit | Le Locle | RandstadAnd final test sequencing. - Ensure that all projects are in compliance with cGMP, cGLP, QSR (including Design Controls), ISO or other applicable requirements. - Support and address comments and suggestions associated with validation and engineering documentation. - Protocol, Deviation, and summary report
Später ansehen12.04.25 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Departments (Production, Engineering, Validation, etc.) to foster an integrated quality approach. - Participate in project meetings and provide expertise on quality aspects related to validations. Your Profile - Degree in a scientific field (pharmacy, biotechnology, chemistry, or equivalent). - Significant
Später ansehen01.02.25 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Project Engineer Fill & Finish 100% (m/w/x) Start Date 20/01/2025 to 28/03/2025 Responsibilities - Serve as the primary technical contact for the project. - Provide input to define Detailed Engineering and project schedules. - Organize and review project activities with internal and external
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