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QC Associate Scientist / ta-330
SimplyVision GmbHNeuchatel, CHVor 30+ Tagen
StellenbeschreibungAuthor transfer protocols and reports for assays Author qualification plans and reports for critical reagents Oversee validation and qualification activities executed by analysts, provide training and support Execute and documents experiments Investigate and trouble shoot problems which occur to determine solutions or recommendations for improvements or change Conduct / participate in risk assessments, root cause analysis and investigations Own Laboratory Investigations and CAPA Support the application of industry specific compliance standards / regulations to assays life cycle management activitiesParticipate to daily activities upon request (provide technical and statistical support) University or engineering degree in analytical chemistry, biotechnology, biochemistry 1 or 2 years of experience in GMP pharma business activities, preferably in the scope of recombinant therapeutic product in pharmaceutical environment Experience in GMP Laboratory activities Good knowledge of method transfer Good knowledge of critical reagent qualification Experience in problem solving and deviation management Good Knowledge of statistical tools Fluent in French and English (C1 written and spoken) Proficiency in all aspects of standard IT tools Excellent collaboration skills and teamwork mindset Good trouble shooting and problem-solving skills Ability to work independently in a fast-paced environment Ability to manage multiple priorities and know when to escalate issues for resolution Effective communicator Demonstrated ability to synthesize information Demonstrated ability to give and receive feedback
For our customer located in Neuchatel / Switzerland we are currently looking for a : QC Associate Scientist (m / f / d)
Tasks & Responsibilities
Duties
The job holder is accountable for life cycle management activities of analytical assays performed in the QC Laboratories of Neuchâtel – Switzerland with a focus on :
- Laboratory Investigations
- Critical Material Qualification
- Laboratory Method Transfers
In addition, the job holder also supports daily QC activities following cGMP, Pharma policies and EHS requirements.
Validation and Qualification Activities
I nvestigation Leads
Quality Control Support Activities
Must Haves
Experience
Competencies