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Jobdetails

Zusammenfassung

    veröffentlicht am 7. mai 2026

    Referenznummer
    25116
    nimm Kontakt mit uns auf

    Wir sind hier, um dir bei deinen Fragen zu helfen.

    M

    Marta Tomczyk

    +41 58 201 55 50

    Nächste Schritte

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    randstad operational

    randstad operational

    We find, nurture, and connect uniquely skilled talent with employers when they need it, building successful teams that scale as their business grows while positioning individuals for rewarding careers and businesses for operational success.

    Jobdetails

    For one of our clients, an international pharma company in Basel, we are currently looking for an Analytical Compliance Record Specialist.



    General Information: ...

     

    • Start date: ASAP
    • Latest start date: August 2026
    • Planned employment duration: 12 months
    • Extension: unlikely
    • Contract: temporary contract via Randstad (employment)
    • Workplace: Basel
    • Workload: 100%
    • Home Office: up to 40%
    • Working Hours: Standard


     

    Tasks & Responsibilities:
     

    • Work in a modern quality control organization in compliance with cGMP regulations.
    • Management of Compliance Records for the department, mainly Deviations, Changes and CAPAs
    • Stakeholder management for the compliance record (including QA, Scientists, Senior Management)
    • Facilitation and Documentation of Root Cause Analyses
    • Active Participation in Quality Review Boards and other strategic and quality relevant governing bodies as needed
    • Inspection Support, including preparation and presentation of records to internal and external auditors / health authority inspectors
    • Critical evaluation of own work results
    • Key role in ensuring an appropriate GMP standard in the department
    • Scientific and regulatory documentation of the work done

     


    Must Haves:
     
    • Advanced Degree (Bachelor’s, Master’s, or higher) in a relevant Natural Science field (e.g., Chemistry, Pharmacy, Biology)
    • Alternative Qualification: Candidates with a Laboratory Technician background will be considered if they possess over 10 years of high-level GMP experience
    • Between 3 to 5 years of professional experience within a regulated pharmaceutical or biotech environment
    • Proven, hands-on experience working under cGMP (current Good Manufacturing Practice) regulations is mandatory
    • QMS Software: Proficiency in Veeva Vault or a comparable Quality Management System (e.g., TrackWise)
    • Core Competencies: Demonstrated ability in managing compliance records, specifically Deviations, Change Control, and CAPAs
    • Business fluency is mandatory (written and spoken) for documentation and stakeholder management
    • Proficiency in German is considered a strong asset and highly beneficial for internal communication
     



    Nice to Haves:
     

    • Prior experience as a Deviation/CAPA Owner or previous experience in a Quality Assurance (QA) role


    Sounds interesting? Apply now - we are looking forward to receiving your application!

    mehr anzeigen

    For one of our clients, an international pharma company in Basel, we are currently looking for an Analytical Compliance Record Specialist.



    General Information:
     

    • Start date: ASAP
    • Latest start date: August 2026
    • Planned employment duration: 12 months
    • Extension: unlikely
    • Contract: temporary contract via Randstad (employment)
    • Workplace: Basel
    • Workload: 100%
    • Home Office: up to 40%
    • Working Hours: Standard


     

    Tasks & Responsibilities:
     

    • Work in a modern quality control organization in compliance with cGMP regulations.
    • Management of Compliance Records for the department, mainly Deviations, Changes and CAPAs
    • Stakeholder management for the compliance record (including QA, Scientists, Senior Management)
    • Facilitation and Documentation of Root Cause Analyses
    • Active Participation in Quality Review Boards and other strategic and quality relevant governing bodies as needed
    • Inspection Support, including preparation and presentation of records to internal and external auditors / health authority inspectors
    • Critical evaluation of own work results
    • Key role in ensuring an appropriate GMP standard in the department
    • Scientific and regulatory documentation of the work done

     


    ...
    Must Haves:
     
    • Advanced Degree (Bachelor’s, Master’s, or higher) in a relevant Natural Science field (e.g., Chemistry, Pharmacy, Biology)
    • Alternative Qualification: Candidates with a Laboratory Technician background will be considered if they possess over 10 years of high-level GMP experience
    • Between 3 to 5 years of professional experience within a regulated pharmaceutical or biotech environment
    • Proven, hands-on experience working under cGMP (current Good Manufacturing Practice) regulations is mandatory
    • QMS Software: Proficiency in Veeva Vault or a comparable Quality Management System (e.g., TrackWise)
    • Core Competencies: Demonstrated ability in managing compliance records, specifically Deviations, Change Control, and CAPAs
    • Business fluency is mandatory (written and spoken) for documentation and stakeholder management
    • Proficiency in German is considered a strong asset and highly beneficial for internal communication
     



    Nice to Haves:
     

    • Prior experience as a Deviation/CAPA Owner or previous experience in a Quality Assurance (QA) role


    Sounds interesting? Apply now - we are looking forward to receiving your application!

    mehr anzeigen
      nimm Kontakt mit uns auf

      Wir sind hier, um dir bei deinen Fragen zu helfen.

      M

      Marta Tomczyk

      +41 58 201 55 50
      verwandte Jobsalle Produktions Und Industrie Manager Jobs in Basel
      • OneStream Senior developer

        • Basel, Basel-Stadt
        • Temporär
        <br /><br />Love complex problems? We’re looking for a OneStream Architect who does more than just configure. We need a seasoned pro with 5+ years of experience and a deep command of C#/VB.NET and Financial Consolidation to lead high-stakes implementations. If you’re a hands-on developer who thrives on building elegant solutions to intricate financial workflows, we want you on the team.<br /><br />General Information:<ul><li>Start date: 01.06.26</li><li>latest Start Date: 01.09.26</li><li>Planned duration: planned until 30.08.2027</li><li>Extension (in case of limitation): possible</li><li>Workload: 80-100%</li><li>Home Office: 50%</li><li>Working hours: Standard</li></ul><br />Tasks & Responsibilities:<ul><li>Design and Development: Contribute to the design, development, testing, and deployment of OneStream solution for finance consolidation, Tax (CbCR & Pillar-two) and ESG, including enhancements, customizations, and integrations.</li><li>System Implementation: Participate in the full lifecycle of our OneStream project, from design to go-live and post-implementation support.</li><li>Technical Leadership: Provide technical support and guidance to co-workers, ensuring adherence to best practices and coding standards and fostering a culture of continuous learning and growth. Advocate for and ensure adherence to OneStream coding standards, best practices, and performance optimization.</li><li>Collaboration: Work closely with functional teams, project managers, and other stakeholders to understand business needs and translate them into technical solutions.</li><li>Documentation: Develop and maintain technical documentation, including design specifications, test plans, and user manuals</li><li>Support and Maintenance: Provide ongoing support and maintenance for OneStream, including troubleshooting and issue resolution.</li></ul><br />Must Haves:<ul><li>Bachelor’s degree in computer science, Systems Engineering, Information Systems, or related field. </li><li>Deep technical expertise in OneStream, with 5+ years of OneStream implementation and development experience (OneStream certification preferred). </li><li>Hands-on configuration and development experience:</li><li>Building and managing dimensions, hierarchies, and member properties.</li><li>Developing complex Business Rules (C#) for calculations, validations, and data transformations. </li><li>Designing and building Cube Views, Dashboards, and Reports.</li><li>Designing and building workflows, user role/permissions & securities.</li><li>Developing data transformation rules (ETL) to map source data to OneStream's data model.</li><li>In-depth understanding of Financial Consolidation topics, month-end close processes and ability to hold discussions with business counterparts.</li><li>Business-focused, results-oriented approach with excellent coordination, exceptional problem-solving, and analytical skills, with a mindset to challenge assumptions, resolve discrepancies and ensure integrity of consolidated results. </li><li>Team and hands-on working style, good organisational skills with ability of multi-task while working independently or within a group environment.</li><li>Ability to work effectively in a project-oriented, fast-paced, deadline-driven environment.</li><li>Excellent interpersonal and customer relationship skills.</li><li>Exceptional communication and influencing skills.</li><li>Business fluent English language skills (written and spoken).</li><li>Hands-on experience in implementing, configuring and developing reporting within the OneStream platform.</li><li>Understanding of modern software architecture, integration tools, and methods (e.g., Data Connectors, APIs, ETL solutions).</li><li>Advanced proficiency in VB.NET or C# and SQL.</li><li>Ability to create technical design documents, and facilitate or validate system and user acceptance testing.</li><li>Participates in knowledge transfer to build internal capacity, advising, and training the internal team on the new application.</li></ul><br /><br />We thank you for your application!
        published on 26. März 2026
      entdecke verwandte Kategorien
      • fertigung-und-materialherstellung
      • produktions-und-industrie-manager
      • qa-analyst

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