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offre d'emploi
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!
montrer plus
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!
montrer plus
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<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!
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