QC Associate Scientist / ta-330

Location
CH-Neuchatel
Start
01.04.2024
End
30.09.2024
Workload
100 %
All-in / Hour
rate negotiable
Total Hours
1048

Deadline:

 

QC Associate Scientist / ta-330

Location
CH-Neuchatel
Workload
100 %

Start

01.04.2024

End

30.09.2024

DEADLINE

  • CH-Neuchatel
  • CH-Neuchatel01.04.202430.09.2024100 % 1048rate negotiable

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

  • 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)

Must Haves

Experience

  • 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

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

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

  • CH-Neuchatel
  • CH-Neuchatel01.04.202430.09.2024100 % 1048rate negotiable

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

  • 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)

Must Haves

Experience

  • 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

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

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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