Process Validation Consultant / no-192

Location
CH-Basel
Start
02.01.2023
End
31.12.2023
Workload
100 %
All-in / Hour
rate negotiable
Total Hours
-

Deadline:

Deadline
28.11.2022

 

Process Validation Consultant / no-192

Location
CH-Basel
Workload
100 %

Start

02.01.2023

End

31.12.2023

DEADLINE

Deadline
28.11.2022

  • CH-Basel
  • CH-Basel02.01.202331.12.2023100 % -rate negotiableDeadline
    28.11.2022

For our customer located in Basel/Switzerland we are currently looking for a: Process Validation Consultant(m/f/d)

 

 

In order to familiarize themselves with the equipment & team, said resources would be on site (Basel) for the first 6 weeks of the project. As of week 7 this can drop to just one day per week on site.

Tasks & Responsibilities

  • Process validation protocols
  • Reports including documentation, data analysis / crunching / conversion into a data plan,
  • once executed assign the data into a report
  • Approx. 20 protocols & related reports are foreseen for the duration of the project

Must Haves

  • BSc. in Chemistry, Biotechnology, Pharmacy or equivalent
  • 5years’+ experience in Biotech manufacturing/ manufacturing science and technology / technical development / regulatory affairs
  • Thorough understanding of Biotech manufacturing processes (mamalian cells) and related process equipment
  • Expertise in writing technical reports in English in ready to submit quality
  • In depth experience in biotech process validation or biotech cleaning validation including plan and report writing > 2 years of experience
  • Basic understanding of standard pharmaceutical analytical testing
  • German written and spoken 

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-Basel
  • CH-Basel02.01.202331.12.2023100 % -rate negotiableDeadline
    28.11.2022

For our customer located in Basel/Switzerland we are currently looking for a: Process Validation Consultant(m/f/d)

 

 

In order to familiarize themselves with the equipment & team, said resources would be on site (Basel) for the first 6 weeks of the project. As of week 7 this can drop to just one day per week on site.

Tasks & Responsibilities

  • Process validation protocols
  • Reports including documentation, data analysis / crunching / conversion into a data plan,
  • once executed assign the data into a report
  • Approx. 20 protocols & related reports are foreseen for the duration of the project

Must Haves

  • BSc. in Chemistry, Biotechnology, Pharmacy or equivalent
  • 5years’+ experience in Biotech manufacturing/ manufacturing science and technology / technical development / regulatory affairs
  • Thorough understanding of Biotech manufacturing processes (mamalian cells) and related process equipment
  • Expertise in writing technical reports in English in ready to submit quality
  • In depth experience in biotech process validation or biotech cleaning validation including plan and report writing > 2 years of experience
  • Basic understanding of standard pharmaceutical analytical testing
  • German written and spoken 

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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