\\n \\n QC ASSOCIATE SCIENTISTExperis is the global leader in professional resourcing and project-based workforce solutions.On behalf of our Pharmaceutical company in Neuchatel we are looking for a QC Associate Scientist for a 12 month Contract opportunity.START DATE: March 17th
DURATION: 12 months
Location: NeuchatelDuties
The job holder is accountable for life cycle management activities of analytical assays performed in the QC
Laboratories of Neuch\\xc3\\xa2tel - 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, 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 executed by analysts, provide

training and support

• Execute and documents experiments

Investigation Leads

• 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

Quality Control Support Activities

• Support the application of industry specific compliance standards/regulations to

assays life cycle management activities

• Participate to daily activities upon request (provide technical and statistical

support)Experience

• University or engineering degree in analytical chemistry, biotechnology, biochemistry, microbiological
• 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

Competencies

• 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

Must haves:
University or engineering degree in analytical chemistry, biotechnology, biochemistry, microbiology
with
University or engineering degree in microbiology
- Experience in GMP laboratory activities
- Experience in problem solving and deviation (event) / lab investigation management
- Strong knowledge of method validation/verification
- Expertise in critical material qualification
- Proficiency in statistical tools
- Fluency in French and English (C1 level in written and spoken)If this job interests you please do send us your CV today through the link in the advert. However, should you have any questions please contact Elaine at +41 61 282 2223\\n \\n \\n \\n \\n \\n

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