no-121

Expert Biologics Analytical Operations / no-121

Location
4056 Basel
Start
17.01.2022
End
31.12.2022
Workload
100 %
All-in / Hour
see job description
Total Hours
1.940h

Deadline:

Deadline
31.12. 12:00pm

 

no-121

Expert Biologics Analytical Operations / no-121

Location
4056 Basel
Workload
100 %

Start

17.01.2022

End

31.12.2022

DEADLINE

Deadline
31.12. 12:00pm

  • 4056 Basel
  • no-1214056 Basel17.01.202231.12.2022100 % 1.940hsee job descriptionDeadline
    31.12. 12:00pm

For our customer located in Basel/Switzerland we are currently looking for a: Expert Biologics Analytical Operations (m/f/d)

  • Location: CH-4056 Basel
  • Branch: pharma
  • Duration: 12 months +
  • gross rate given by client: 40,37 – 45,00 chf/h

Tasks & Responsibilities

As expert, you are supporting the release and stability strategy, the method validation and method transfer activities for our products covering development activities.
You will support the operational aspects of GMP testing of Biologics clinical drug substances (DS) and drug products (DP). You independently manage your activities and provide required documentation according to agreed timelines and standards.

  • Responsible for the successful delivery of work packages to support GMP testing of Biologics clinical drug substances (DS) and drug products (DP) for release/stability/validation/transfer
  • Author and/or review of technical source documents in accordance with project timelines for global submissions
  • Review high-quality CMC documentation for HA submission

Must Haves

  • Well-developed planning, organizational, problem solving and interpersonal skills
  • Good communication skills with a collaborative and patient-focused mindset
  • Computer/IT systems literacy

Nice to Haves

  • Education Minimum: Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent; advanced degree desired
  • Minimum 2 years of Quality Control experience in a GMP environment and/or pharmaceutical industry experience
  • Sound technical and scientific knowledge of pharmaceutical development and analytical sciences
  • Knowledge on health authority regulations
  • Proven ability to critically evaluate data from a broad range of scientific disciplines
  • Proficient in English (other languages are a plus)

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.

Tagged as: CMC, drug products, drug substances, GMP, Testing, validation

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.

  • 4056 Basel
  • no-1214056 Basel17.01.202231.12.2022100 % 1.940hsee job descriptionDeadline
    31.12. 12:00pm

For our customer located in Basel/Switzerland we are currently looking for a: Expert Biologics Analytical Operations (m/f/d)

  • Location: CH-4056 Basel
  • Branch: pharma
  • Duration: 12 months +
  • gross rate given by client: 40,37 – 45,00 chf/h

Tasks & Responsibilities

As expert, you are supporting the release and stability strategy, the method validation and method transfer activities for our products covering development activities.
You will support the operational aspects of GMP testing of Biologics clinical drug substances (DS) and drug products (DP). You independently manage your activities and provide required documentation according to agreed timelines and standards.

  • Responsible for the successful delivery of work packages to support GMP testing of Biologics clinical drug substances (DS) and drug products (DP) for release/stability/validation/transfer
  • Author and/or review of technical source documents in accordance with project timelines for global submissions
  • Review high-quality CMC documentation for HA submission

Must Haves

  • Well-developed planning, organizational, problem solving and interpersonal skills
  • Good communication skills with a collaborative and patient-focused mindset
  • Computer/IT systems literacy

Nice to Haves

  • Education Minimum: Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent; advanced degree desired
  • Minimum 2 years of Quality Control experience in a GMP environment and/or pharmaceutical industry experience
  • Sound technical and scientific knowledge of pharmaceutical development and analytical sciences
  • Knowledge on health authority regulations
  • Proven ability to critically evaluate data from a broad range of scientific disciplines
  • Proficient in English (other languages are a plus)

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.

Tagged as: CMC, drug products, drug substances, GMP, Testing, validation

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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