Quality Control Analyst / ta-472

Location
CH-Neuchatel
Start
asap
End
28.03.2025
Workload
100 %
All-in / Hour
rate negotiable
Total Hours
8288

Deadline:

Deadline
02.04.2024

 

Quality Control Analyst / ta-472

Location
CH-Neuchatel
Workload
100 %

Start

asap

End

28.03.2025

DEADLINE

Deadline
02.04.2024

  • CH-Neuchatel
  • CH-Neuchatelasap28.03.2025100 % 8288rate negotiableDeadline
    02.04.2024

For our customer located in Neuchatel/ Switzerland we are currently looking for a: Quality Control Analyst (m/w/d)


You will bring solid laboratory experience, including biochemical methods such as ELISA, enzymatic activity, Western Blot, etc., to your role. Through your work as a laboratory technician, you have developed a good theoretical and practical understanding of biochemical methods and technology.

In particular, we expect:

  • You work in a structured and quality-oriented way.
  • You find satisfaction and motivation in routine tasks.
  • You have experience of good manufacturing practice (cGMP).

We prefer a relaxed, close-knit environment. You work in a team where tasks change very quickly. We therefore expect you to be motivated by a fast-changing environment while being able to deliver high-level results.

Tasks & Responsibilities

  • Carry out biochemical analysis and supervision activities in accordance with laboratory procedures, GMP/BPD rules and/or projects in line with Quality Control department activities.
  • Comply with all procedures in force
  • Respect and apply EHS rules.
  • Complete the various forms, logbooks and documents in compliance with Good Manufacturing and Documentation Practices and ALCOA +.
  • Notify the Supervisor of any non-conforming and/or invalid results on the same day, orally and/or in writing, and initiate the event in the quality system within the set deadlines.
  • Manage laboratory investigations.
  • Apply planning requests and report any concerns proactively.
  • Carry out reagent/consumable qualification and validation protocols (method, system, equipment).
  • Ensure that equipment calibration and maintenance is in order during analysis.
  • Respect real-time Kanban management
  • Report procedural deviations to method/equipment manager and Supervisor/Delegate/Expert
  • Be able to identify and solve certain less complex problems relating to its area of expertise (Troubleshooting)
  • Carry out or approve solutions in the laboratory.
  • Manage and tidy the laboratory in general, respecting 5S standardization standards.
  • Support continuous improvement initiatives.

Must Haves

  • Minimum level of education: CFC laboratory/biology or other relevant scientific field.
  • Minimum 3 years’ experience in a QC laboratory in a cGMP environment.
  • Experience in electrophoresis analysis, Elisa, or enzyme activity determination desirable
  • Fluent French and technical English
  • Swiss or EU nationality, or valid Swiss work permit

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-Neuchatelasap28.03.2025100 % 8288rate negotiableDeadline
    02.04.2024

For our customer located in Neuchatel/ Switzerland we are currently looking for a: Quality Control Analyst (m/w/d)


You will bring solid laboratory experience, including biochemical methods such as ELISA, enzymatic activity, Western Blot, etc., to your role. Through your work as a laboratory technician, you have developed a good theoretical and practical understanding of biochemical methods and technology.

In particular, we expect:

  • You work in a structured and quality-oriented way.
  • You find satisfaction and motivation in routine tasks.
  • You have experience of good manufacturing practice (cGMP).

We prefer a relaxed, close-knit environment. You work in a team where tasks change very quickly. We therefore expect you to be motivated by a fast-changing environment while being able to deliver high-level results.

Tasks & Responsibilities

  • Carry out biochemical analysis and supervision activities in accordance with laboratory procedures, GMP/BPD rules and/or projects in line with Quality Control department activities.
  • Comply with all procedures in force
  • Respect and apply EHS rules.
  • Complete the various forms, logbooks and documents in compliance with Good Manufacturing and Documentation Practices and ALCOA +.
  • Notify the Supervisor of any non-conforming and/or invalid results on the same day, orally and/or in writing, and initiate the event in the quality system within the set deadlines.
  • Manage laboratory investigations.
  • Apply planning requests and report any concerns proactively.
  • Carry out reagent/consumable qualification and validation protocols (method, system, equipment).
  • Ensure that equipment calibration and maintenance is in order during analysis.
  • Respect real-time Kanban management
  • Report procedural deviations to method/equipment manager and Supervisor/Delegate/Expert
  • Be able to identify and solve certain less complex problems relating to its area of expertise (Troubleshooting)
  • Carry out or approve solutions in the laboratory.
  • Manage and tidy the laboratory in general, respecting 5S standardization standards.
  • Support continuous improvement initiatives.

Must Haves

  • Minimum level of education: CFC laboratory/biology or other relevant scientific field.
  • Minimum 3 years’ experience in a QC laboratory in a cGMP environment.
  • Experience in electrophoresis analysis, Elisa, or enzyme activity determination desirable
  • Fluent French and technical English
  • Swiss or EU nationality, or valid Swiss work permit

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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