R&D Quality Specialist / no-276

Location
CH-Basel
Start
01.02.2023
End
30.07.2024
Workload
100 %
All-in / Hour
rate negotiable
Total Hours
3128

Deadline:

 

R&D Quality Specialist / no-276

Location
CH-Basel
Workload
100 %

Start

01.02.2023

End

30.07.2024

DEADLINE

  • CH-Basel
  • CH-Basel01.02.202330.07.2024100 % 3128rate negotiable

For our customer located in Basel/Switzerland we are currently looking for a: R&D Quality Specialist(m/f/d)

Tasks & Responsibilities

  • Support the supervisor in the timely release of GMP relevant documents.
  • Support departmental projects and objectives according to agreed timelines and standards in the given area of competency and support adherence to compliance with GMP in TRD.
  • Identify and execute on OpEx opportunities.
  • Build/manage stakeholder relationships and expectations.
  • Perform review of GMP relevant documents for compliance with SOPs (e.g. review of analytical raw data and analytical documents).
  • Clarify simple deficiencies in GMP documents with the line unit experts in own responsibility.
  • Recognize complex deficiencies in GMP documents, report them to supervisor, suggest actions and supervise agreed follow-up.
  • Write and complete GMP relevant documents in own area of responsibility (e.g CoAs, BRR sheets).
  • File and archive documents owned by QA
  • Collaborate with other associates to support the service function of QA
  • Participate in knowledge exchange in TRD.
  • Participate in training of new and temporary employees

Must Haves

  • specific GxP experience
  • Experience within R&D Quality
  • pharma experience
  • Basic financial knowledge (e.g., cost management, budget forecast, etc.)

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-Basel01.02.202330.07.2024100 % 3128rate negotiable

For our customer located in Basel/Switzerland we are currently looking for a: R&D Quality Specialist(m/f/d)

Tasks & Responsibilities

  • Support the supervisor in the timely release of GMP relevant documents.
  • Support departmental projects and objectives according to agreed timelines and standards in the given area of competency and support adherence to compliance with GMP in TRD.
  • Identify and execute on OpEx opportunities.
  • Build/manage stakeholder relationships and expectations.
  • Perform review of GMP relevant documents for compliance with SOPs (e.g. review of analytical raw data and analytical documents).
  • Clarify simple deficiencies in GMP documents with the line unit experts in own responsibility.
  • Recognize complex deficiencies in GMP documents, report them to supervisor, suggest actions and supervise agreed follow-up.
  • Write and complete GMP relevant documents in own area of responsibility (e.g CoAs, BRR sheets).
  • File and archive documents owned by QA
  • Collaborate with other associates to support the service function of QA
  • Participate in knowledge exchange in TRD.
  • Participate in training of new and temporary employees

Must Haves

  • specific GxP experience
  • Experience within R&D Quality
  • pharma experience
  • Basic financial knowledge (e.g., cost management, budget forecast, etc.)

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.

SIGN IN JOB ALERT