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Qc associate scientist

Neuenburg
Experis
EUR 30’000 - EUR 80’000 pro Jahr
Inserat online seit: Veröffentlicht vor 15 Std.
Beschreibung

Experis is the global leader in professional resourcing and project-based workforce solutions.

On behalf of our Pharmaceutical company in Neuchâtel, we are seeking a QC Associate Scientist for a 12-month contract.

Start Date: March 17th

Duration: 12 months

Location: Neuchâtel


Duties

The job holder is responsible for life cycle management activities of analytical assays in the QC laboratories of Neuchâtel, Switzerland, focusing on:

* Laboratory Investigations
* Critical Material Qualification
* Laboratory Method Transfers

Additionally, supports daily QC activities adhering to cGMP, policies, and EHS requirements.


Validation and Qualification Activities

* Author transfer protocols and reports for assays
* Author qualification plans and reports for critical reagents
* Oversee validation and qualification activities performed by analysts


Training and Support

* Execute and document experiments


Investigation Leads

* Investigate and troubleshoot issues to determine solutions or improvements
* Conduct/risk assessments, root cause analysis, and investigations
* Manage Laboratory Investigations and CAPA


Quality Control Support Activities

* Apply industry-specific compliance standards/regulations
* Participate in daily activities, providing technical and statistical support as needed


Experience and Qualifications

* University or engineering degree in analytical chemistry, biotechnology, biochemistry, microbiology
* 1-2 years of GMP pharmaceutical experience, preferably with recombinant therapeutic products
* Experience in GMP laboratory activities, method transfer, and critical reagent qualification
* Problem solving and deviation management skills
* Knowledge of statistical tools
* Fluent in French and English (C1 level)
* Proficiency with standard IT tools
* Excellent collaboration, troubleshooting, and independent working skills


Must-Haves

* Degree in microbiology or related fields
* Experience in GMP lab activities, problem solving, deviation management
* Strong knowledge of method validation and critical material qualification
* Fluency in French and English (C1 level)

If interested, please send your CV via the link in the advert. For questions, contact Elaine at +41 61 282 2223.

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