Lab IT specialist (6517)

CTC Resourcing Solutions; Basel; Vor Ort; CHF 80’000 - 120’000; Vollzeit

Zusammenfassung

A leading player in the Pharmaceutical industry is seeking a Lab IT Specialist for an 18-month contract in Basel, Switzerland. The ideal candidate will manage IT systems, contribute to digital tool implementations, and ensure GMP compliance. Applicants should have 3-5 years of experience in the pharmaceutical sector, strong organizational skills, and the ability to work in a dynamic environment.

Qualifikationen

• 3-5 years’ experience in the pharmaceutical industry or IT systems.
• Good proficiency in English; German or French is a plus.
• Ability to work independently and responsibly.

Aufgaben

• Contribute to digital tools and lab digitalization.
• Act as Single Point of Contact for ARD colleagues.
• Ensure GMP compliance for all relevant activities.

Kenntnisse

IT systems/tools expertise

data reporting/analysis

organizational skills

GMP/Data Integrity knowledge

communication skills

collaboration/team spirit

Tools

LIMS systems

Microsoft Office

Jobbeschreibung

The Life Science Career Network– CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.

Lab IT Specialist –6517

Our client is a leading global player in the Pharmaceutical industry with global headquarters in Basel, Switzerland.

We are currently looking for a Lab IT Specialist for an initial 18-months contract starting first of July 2025 until the end of 2026, to be based in Basel, Switzerland.

The perfect candidate is a highly motivated expert in IT systems/tools, with extended expertise in IT system ownership and management, knowledge in data reporting/analysis/insights, and good overall organizational skills. Additional knowledge and experience in continuous improvement/operational excellence, and analytical chemistry/quality control environment is a plus.

Main Responsibilities:

• Contribute to projects, initiatives and implementation of digital tools, lab digitalization, process excellence, continuous improvement, and change management with focus on ARD Science & Operations CH.

• Hold certain roles in selected digital tools to support user community, content management and processes, as needed.

• Provide flexible support for ARD analytical/QC labs, as needed.

• Act as Single Point of Contact (SPoC) for ARD colleagues on identified projects.

• Ensure GMP compliance for all GMP relevant activities in alignment with regulations and decisions.

• Work according to appropriate SOPs, GMP, ALCOA+, Quality Directives, Health and Safety (HSE) regulations and internal guidelines, as needed.

Qualifications and Experience:

• Relevant working/residency permit or Swiss/EU-Citizenship required

• 3-5 years’ experience in the pharmaceutical industry or other field, preferred in the field of IT systems/digital tools and analytical chemistry/quality control.

• Knowledgeable and agile in using different software.

• GMP/Data Integrity knowledge.

• Excellent organizational skills, collaboration, and team spirit and customer orientation.

• Good communication skills

• Ability to perform in a highly dynamic environment

• Proficiency with Microsoft Office and other data software, preferably LIMS systems.

• Good proficiency in English (oral and written), good proficiency in German or French is a plus.

• Ability to work independently and responsibly

• Fast understanding of tasks

Would you like to learn more about CTC and the opportunity outlined?Please, get in contact with us:you may either use the 'apply now' button, or write an email to us, or reach out to us on the phone.