Associate Expert in Technical Research and Development / no-968

Location
Basel
Start
asap/01.08.2022
End
31.12.2022
Workload
100 %
All-in / Hour
see Job Description
Total Hours
888

Deadline:

Deadline
03.08.2022

 

Associate Expert in Technical Research and Development / no-968

Location
Basel
Workload
100 %

Start

asap/01.08.2022

End

31.12.2022

DEADLINE

Deadline
03.08.2022

  • Basel
  • Baselasap/01.08.202231.12.2022100 % 888see Job DescriptionDeadline
    03.08.2022

For our customer located in Basel/Switzerland we are currently looking for a: Associate Expert in Technical Research and Development (m/f/x)


  • Pay Rate range (given by client: 31.87 CHF/h – 35.86 CHF/h

Tasks & Responsibilities

Job Purpose:
The line function Analytical Research and Development (ARD) is part of the Global Technical R&D department of Global Drug Development (GDD) and plays an essential role in the characterization and analysis of small molecules and synthetic large molecules Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production.
We are looking for a highly motivated scientist with experience in area of sampling.

Major accountabilities:

  • Meet quality, quantity and timelines in all assigned projects
  • Ensure GMP compliance for all GMP relevant analytical activities of assigned projects in alignment with the company’s regulations and network decisions
  • Work according to appropriate SOPs, GMP, ALCOA+, Quality Directives, Health and Safety (HSE) regulations and internal guidelines.
  • Sampling (dispensing task) from warehouse bulk containers
    o Partially in full protective suit
    o Partially physically hard work (pallet movements, etc.)
    o Work in various clean zones
  • If necessary emergency service (“Pikettdienst”)
  • Electronic inventory management with GLIMS and SAP
  • Transport of pharmaceutical products

Must Haves

In order to successfully fulfill this role, you should bring following qualifications:

 

  • 3-5 years’ experience in the pharmaceutical industry, preferred analytical development in the field of sampling and sample portioning
  • GMP/Data Integrity knowledge
  • Proficiency with Microsoft Office and other data software
  • ADR1.3 and ADR1.10 certificate advantageous
  • Car driving license (mandatory)
  • Good knowledge in English and German (oral and in writing)
  • Committed, well thought-out and flexible teamwork
  • Independent working method
  • Fast comprehension task

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.

  • Basel
  • Baselasap/01.08.202231.12.2022100 % 888see Job DescriptionDeadline
    03.08.2022

For our customer located in Basel/Switzerland we are currently looking for a: Associate Expert in Technical Research and Development (m/f/x)


  • Pay Rate range (given by client: 31.87 CHF/h – 35.86 CHF/h

Tasks & Responsibilities

Job Purpose:
The line function Analytical Research and Development (ARD) is part of the Global Technical R&D department of Global Drug Development (GDD) and plays an essential role in the characterization and analysis of small molecules and synthetic large molecules Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production.
We are looking for a highly motivated scientist with experience in area of sampling.

Major accountabilities:

  • Meet quality, quantity and timelines in all assigned projects
  • Ensure GMP compliance for all GMP relevant analytical activities of assigned projects in alignment with the company’s regulations and network decisions
  • Work according to appropriate SOPs, GMP, ALCOA+, Quality Directives, Health and Safety (HSE) regulations and internal guidelines.
  • Sampling (dispensing task) from warehouse bulk containers
    o Partially in full protective suit
    o Partially physically hard work (pallet movements, etc.)
    o Work in various clean zones
  • If necessary emergency service (“Pikettdienst”)
  • Electronic inventory management with GLIMS and SAP
  • Transport of pharmaceutical products

Must Haves

In order to successfully fulfill this role, you should bring following qualifications:

 

  • 3-5 years’ experience in the pharmaceutical industry, preferred analytical development in the field of sampling and sample portioning
  • GMP/Data Integrity knowledge
  • Proficiency with Microsoft Office and other data software
  • ADR1.3 and ADR1.10 certificate advantageous
  • Car driving license (mandatory)
  • Good knowledge in English and German (oral and in writing)
  • Committed, well thought-out and flexible teamwork
  • Independent working method
  • Fast comprehension task

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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