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47 Hits

Jobs by e-mail

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    Reference number: 853873/1

    QA Specialist - CSV & Automation (m/f/d)

    Freelance/temporary employment for a project
    Stein
    • Ensure qualification and validation plans for equipment, infrastructure, and computerized systems comply with Lonza Quality policies
    • Review and approve SOPs, commissioning/qualification/validation protocols, reports, and CQV/CSV documentation (e.g., URS, FAT/SAT)
    • Provide QA leadership and guidance on qualification/validation topics for large-scale CAPEX projects
    • Act as primary QA contact for lifecycle compliance of equipment and computerized systems, including documentation in global systems (Kneat, Trackwise, DMS, Unifier)
    • Oversee vendor qualification and ensure adherence to GMP standards
    • Manage quality deviations, changes, and CAPAs, ensuring timely resolution and escalation when necessary
    • Support project teams during design, commissioning, and qualification phases for aseptic fill-finish facilities
    • Collaborate cross-functionally to maintain compliance throughout project execution
    • Contribute to continuous improvement initiatives in QA processes and systems
    • Ensure compliance with regulatory requirements and internal quality standards
    Online since: Thu Dec 11 14:56:22 CET 2025
    Reference number: 853720/1

    Laboratory Associate Sampling (m/f/d)

    Freelance/temporary employment for a project
    Lengnau, Berne
    • Participate in sampling sessions for plant and clean utilities, environmental monitoring and raw materials
    • Sample logistics (receipt, storage, SM LIMS registration, aliquoting, distribution and disposition of samples)
    • Support of raw material sampling sessions at external warehouse (3PL)
    • Supporting external shipment of QC samples (third party laboratories, suppliers or customers)
    • Daily laboratory maintenance (support, washers, waste disposal)
    Online since: Thu Dec 11 08:41:22 CET 2025
    Reference number: 853459/1

    Production Operator (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Perform production tasks across facilities while ensuring compliance with safety regulations and cGMP quality standards
    • Identify, interpret, and resolve deviations in production processes to maintain efficiency and quality
    • Execute production steps with precision, including documentation, calculations, and reporting
    • Support onboarding and training of new team members to strengthen team knowledge and performance
    Online since: Tue Dec 09 14:46:07 CET 2025
    Reference number: 853393/1

    In-Vivo Laboratory Worker (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Conduct in vivo studies with rodents and rabbits in toxicology and pharmacokinetics
    • Perform clinical scoring and health monitoring of laboratory animals
    • Collect blood samples and administer dosing via multiple routes (IP, IV, PO, Subcutaneous)
    • Carry out basic necropsy procedures and tissue collection
    • Document, review, and verify study data in forms or electronic capture systems
    • Participate in weekend study activities on a rotational basis
    • Optionally assist in surgical procedures, including anesthesia, and provide pre- and postoperative care
    • Ensure compliance with animal welfare standards and best veterinary practices
    Online since: Tue Dec 09 14:06:19 CET 2025
    Reference number: 853098/1

    Senior Data Scientist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Perform ad-hoc literature searches in biomedical databases to identify adverse drug reactions and risks
    • Develop, test, document, and maintain search profiles for published case reports and safety updates
    • Create and manage search profiles for Development Safety Update Reports (DSURs), PBRERs, and signal detection
    • Build search profiles to identify incidents and risks in association with medical devices (MDIRs, signal detection)
    • Conduct efficacy searches in biomedical databases to support safety and medical affairs reporting
    • Collaborate with stakeholders to define search criteria and ensure plausibility of results
    • Deliver timely and compliant search results in line with SOPs and regulatory requirements
    • Contribute to the Safety Literature Group, knowledge sharing, training, and process improvements
    Online since: Mon Dec 08 10:40:47 CET 2025
    Reference number: 853060/1

    Senior Director Total Rewards (m/f/d)

    Freelance/temporary employment for a project
    Basel
    • Lead the global Total Rewards strategy for CHI, ensuring alignment with business objectives and organizational culture
    • Partner with HR Leadership and HRBPs to deliver strategic and operational reward solutions across 3,500+ employees
    • Provide expert consultation on compensation, benefits, payroll, and global HR services to senior stakeholders
    • Drive pay transparency initiatives and embed a strong pay-for-performance culture
    • Manage compensation aspects of mergers, acquisitions, and organizational changes, ensuring smooth integration
    • Oversee annual market benchmarking, salary structures, grading systems, and compliance with global/local regulations
    • Develop and implement communication and education tools for Total Rewards programs to enhance understanding and adoption
    • Recommend innovative reward solutions to attract, motivate, and retain top talent globally
    • Ensure governance and policy adherence, acting as a trusted advisor on interpretation and application
    • Lead and mentor a small team, fostering collaboration and professional growth
    Online since: Mon Dec 08 08:17:24 CET 2025
    Reference number: 852900/1

    Technical R&D Associate Scientist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Development, improvement and validation of analytical methods for the quality assessment of starting materials, intermediates, reaction monitoring, active substances and galenical forms
    • Thorough and efficient planning, execution and documentation of experiments in collaboration with the relevant team members, analytical project lead and your supervisor, following current GxP guidelines as well as relevant SOPs
    • Work on end-to-end processes in close collaboration with other associate scientists, scientists, and partners from other departments to ensure efficient analytics and continuous improvement
    • Coordination of analytical activities, including sample management for the development of synthetic productsAuthoring of documents, e.g., analytical procedures, validation reports, user manuals, SOPs
    Online since: Fri Dec 05 14:24:06 CET 2025
    Reference number: 852860/1

    Drug Product - Project Champion (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Lead technical expansion and capacity increase projects within Drug Product manufacturing to support production ramp-up
    • Provide technical input to project design, ensuring compliance with operational needs and regulatory standards (e.g., EU GMP Annex 1)
    • Coordinate cross-functional teams and external suppliers, manage project governance, and ensure delivery on time and within scope
    • Develop and implement best-practice processes aligned with current industry and regulatory trends
    • Manage change control, troubleshooting, and deviations related to projects and equipment
    • Establish and update operational procedures in collaboration with manufacturing and quality functions
    Online since: Fri Dec 05 09:18:17 CET 2025
    Reference number: 852381/1

    Manager Regulatory Affairs (m/f/d)

    Freelance/temporary employment for a project
    Zurich
    • Lead regulatory activities for vaccine projects, including submissions and lifecycle management
    • Prepare and manage Marketing Authorization Applications (MAA) and variations in compliance with EMA and local regulations
    • Ensure timely and accurate regulatory documentation and filings
    • Provide oversight for assigned clinical trials and related regulatory requirements
    • Collaborate with global and regional teams to align regulatory strategies
    • Support health authority interactions and meetings in the region
    • Maintain regulatory archives and manage documentation in EDMS
    • Track regulatory commitments and activities in internal systems
    Online since: Wed Dec 03 09:39:09 CET 2025
    Reference number: 851966/1

    Supply Chain Clerk (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Maintain and continuously improve the production schedule within an 8-week horizon
    • Coordinate timely delivery of API and raw materials from warehouse to production lines
    • Ensure accurate posting of material consumption and labor/machine hours in ERP systems
    • Manage urgent material re-orders and resolve scheduling conflicts proactively
    • Monitor production data (volumes, material usage, quality) for continuous improvement
    • Generate KPIs and operational metrics to identify trends and optimize performance
    • Oversee QC raw material release to meet production timelines
    • Allocate material lots to production orders under FEFO principles and compliance standards
    • Track supplier purchase orders and take corrective actions for delays or shortages
    • Ensure short-term changes are reflected in the schedule and communicated to stakeholders
    Online since: Mon Dec 01 11:05:43 CET 2025

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    Reference number: 851539/1

    Senior Scientist QC Micobiology (m/f/d)

    Freelance/temporary employment for a project
    Lengnau, Berne
    • Perform microbiological testing (operations, validation, utilities, environmental monitoring)
    • Support transfer, development and validation of analytical methods
    • Execute qualification, calibration and maintenance of laboratory equipment
    • Ensure GMP inspection readiness and compliance with all Quality System documentation
    • Contribute to QC operational readiness, including project coordination
    • Coordinate daily tasks within the QC team
    • Create and revise SOPs, Work Instructions and other QC-related documents
    Online since: Thu Nov 27 15:02:40 CET 2025
    Reference number: 851387/1

    QA Batch Record Reviewer (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Review executed batch records, including production documentation and raw data
    • Support batch release by verifying the completeness and accuracy of documentation packages
    • Assess comments added to batch records, clarify with operations teams, and evaluate findings with the responsible QA Manager
    • Initiate deviations and investigations related to observations during batch record review
    • Collaborate closely with QA and production teams to maintain compliance and resolve discrepancies
    Online since: Wed Nov 26 16:01:35 CET 2025
    Reference number: 850734/1

    Technical Project Lead – GMP Environment (m/f/d)

    Freelance/temporary employment for a project
    Stein
    • Lead technical coordination for assigned systems across construction, commissioning, and qualification phases
    • Act as the primary technical point of contact for approx. 10 systems
    • Interpret and manage PNIDs to ensure system integration and compliance
    • Coordinate with vendors and third parties for equipment specifications and delivery
    • Oversee engineering preparation during construction; ensure readiness before building completion
    • Perform technical quality checks and validate engineering deliverables
    • Ensure seamless collaboration between black utilities, clean utilities, and process equipment
    • Define and maintain unified technical standards to reduce costs and ensure compliance
    • Support technical compliance requirements (e.g., ATEX, fire protection)
    • Promote safety culture and proactive communication within a large multidisciplinary team
    Online since: Mon Nov 24 08:42:45 CET 2025
    Reference number: 850280/1

    Scientist (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Technical representation of QC Microbiology during internal reviews, customer meetings, audits, site visits, and inspections
    • Scientific SME support for project-specific microbial analyses, including monitoring, evaluating, and coordinating the implementation of improvements
    • Coordination of work packages assigned to business units (BUs), ensuring timely completion and alignment with project objectives
    • Facilitation of communication across interdisciplinary teams (e.g., studies, validation/verification, deviations, transfers)
    • Continuous improvement of QC Microbiology processes in line with regulatory standards and industry best practices
    Online since: Fri Nov 21 14:55:16 CET 2025
    Reference number: 849910/1

    Clinical Scientist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Analyse and interpret clinical data in collaboration with Biostatistics and Data Management
    • Robust experience in data review and data cleaning to ensure data quality and data integrity
    • Scientific support in the conduct and evaluation of clinical trials (phase II-III) with a focus on rare diseases
    • Preparation and review of study documents (e.g. protocols, IBs, CSRs)
    • Close collaboration with interdisciplinary teams as part of the study management team (Clin Ops, DM, Stats, Regulatory Affairs, etc.)
    • Support in communication with trial sites, CROs and authorities
    • Contribute to the development of internal and external presentations
    Online since: Fri Nov 21 13:17:32 CET 2025
    Reference number: 848825/1

    Global Clinical Program Manager (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Act as a planning expert in Clinical Operations Program Leadership, managing project information for decision-making across CDMA teams and leadership
    • Apply project management skills and clinical operations expertise to ensure timely, budget-compliant delivery of CDMA-related outcomes
    • Collaborate with other Clinical Program Managers, Portfolio & Project Management Office staff, and leadership to align deliverables
    • Drive patient- and customer-centricity by prioritizing patient needs and customer satisfaction in all activities
    • Partner across diverse regions and cultures to foster inclusion, belonging, and diversity within teams
    • Identify opportunities for collaboration across Clinical Development and Medical Affairs communities
    • Lead project management activities such as budget planning, tracking, reporting, risk management, and change management within clinical operations or diagnostic product development
    • Guide teams in resolving complex issues, influencing senior stakeholders to adopt new approaches and improve organizational outcomes
    Online since: Tue Nov 11 15:10:49 CET 2025
    Reference number: 848817/1

    Global Project Manager (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Set up and implement project, program, and product structures for development and product care activities
    • Create and maintain integrated project plans including dependencies, resources, and budgets
    • Ensure quality implementation in risk management, critical path analysis, scenario planning, and budget control
    • Guide teams through milestone reviews, capacity reviews, and continuous improvement initiatives
    • Apply project methodologies, including agile practices, and coach teams in hybrid agile/non-agile approaches
    • Manage meetings, knowledge sharing, and foster positive team dynamics
    • Establish and report KPIs, OKRs, and other metrics to measure project success
    • Identify risks, bottlenecks, and propose solutions to keep projects on track while communicating proactively with stakeholders
    Online since: Tue Nov 11 15:09:51 CET 2025
    Reference number: 847881/1

    Senior Associate in automated cell culture (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Operate and maintain automated cell culture systems for large-scale cell production
    • Support HTS campaigns and profiling assays by executing automated experiments
    • Plan experiments, order materials, and run biochemical and cellular assays on automated platforms
    • Analyze assay data and troubleshoot issues in workflows or automation systems
    • Collaborate with assay development teams across cellular, biochemical, biophysical, MS, and RNA domains
    • Contribute to the design of new cell culture systems with external vendors (optional)
    • Expand knowledge in lab automation and digital workflows
    • Work within a dynamic, inclusive matrix team focused on drug discovery
    Online since: Mon Nov 10 08:22:02 CET 2025
    Reference number: 847769/1

    Laboratory Specialist QC (m/f/d)

    Freelance/temporary employment for a project
    Lengnau, Berne
    • Performs testing in the Bio-/ Chemical Quality Control (BCQC) of final and intermediate products, in process samples, samples from cleaning validation, utilities and environmental monitoring samples
    • Supports the transfer, development and validation of analytical methods including qualification of equipment needed for analysis
    • Participation in maintenance, calibration and use of laboratory equipment
    • Participation in the training and qualification of new employees
    • Creation and revision of guidance documents such as SOPs/ WIs and other related documents
    • Supports the QC Support team during the project phase in the ordering of material and inventory management of the QC laboratories
    Online since: Wed Nov 05 13:47:49 CET 2025
    Reference number: 845943/1

    Data & Digital Workflow Specialist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Enhance data accessibility and interoperability using FAIR principles
    • Analyze and optimize digital workflows across scientific and lab environments
    • Streamline and maintain data pipelines for improved usability and performance
    • Lead product development and rollout of digital solutions
    • Conduct user training and manage change initiatives across teams
    • Document workflows and ensure consistent system usage
    • Act as liaison between IT, business units, and end-users 
    • Report progress and insights to leadership and stakeholders
    Online since: Fri Oct 24 13:41:00 CEST 2025
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