EXPIRED-QA Associate / no-640

Location
CH-Basel
Start
asap
End
18 months
Workload
100 %
All-in / Hour
see job description
Total Hours
3.144

Deadline:

Deadline
EXPIRED

 

EXPIRED-QA Associate / no-640

Location
CH-Basel
Workload
100 %

Start

asap

End

18 months

DEADLINE

Deadline
EXPIRED

  • CH-Basel
  • CH-Baselasap18 months100 % 3.144see job descriptionDeadline
    EXPIRED

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

  • Location: CH-Basel
  • Branch: Pharma
  • Duration: asap – 18 months
  • Payrate: max. 42 chf/h

Tasks & Responsibilities

  • Support a discipline and/or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility
  • Write and review GMP-relevant deliverables and/or related tools as per area of responsibility in order to ensure compliance with cGMP and project quality deliverables.
  • Comply with internal and external guidelines regarding quality and safety (Quality Manual, regulatory cGMP guidelines, Health Authority guidances, SOPs etc.).
  • Manufacturing and analytical Batch Record Review for batches of the CHAD department (internal/external)
  • Support paper archiving in TRD QA Ops NCE
  • Support the timely release of GMP relevant documents and batches.
  • Support departmental projects and objectives according to agreed timelines and standards in the given area of competency and support adherence to compliance with cGMP in TRD.

Must Haves

  • Education: either Technician with 5 years’ experience OR Bachelor with 3 years’ experience
  • Languages: Fluent German, English required (adequate knowledge oral & written)
  • Scientific, technical and regulatory knowledge in a specific area.
  • Detailed knowledge of cGM
  • Working knowledge of safety and environmental regulations and guidelines.
  • Communication skills to sufficiently address GMP and logistic related questions with line unit experts.
  • Basic knowledge of drug development.
  • Good organizational skills.

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-Baselasap18 months100 % 3.144see job descriptionDeadline
    EXPIRED

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

  • Location: CH-Basel
  • Branch: Pharma
  • Duration: asap – 18 months
  • Payrate: max. 42 chf/h

Tasks & Responsibilities

  • Support a discipline and/or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility
  • Write and review GMP-relevant deliverables and/or related tools as per area of responsibility in order to ensure compliance with cGMP and project quality deliverables.
  • Comply with internal and external guidelines regarding quality and safety (Quality Manual, regulatory cGMP guidelines, Health Authority guidances, SOPs etc.).
  • Manufacturing and analytical Batch Record Review for batches of the CHAD department (internal/external)
  • Support paper archiving in TRD QA Ops NCE
  • Support the timely release of GMP relevant documents and batches.
  • Support departmental projects and objectives according to agreed timelines and standards in the given area of competency and support adherence to compliance with cGMP in TRD.

Must Haves

  • Education: either Technician with 5 years’ experience OR Bachelor with 3 years’ experience
  • Languages: Fluent German, English required (adequate knowledge oral & written)
  • Scientific, technical and regulatory knowledge in a specific area.
  • Detailed knowledge of cGM
  • Working knowledge of safety and environmental regulations and guidelines.
  • Communication skills to sufficiently address GMP and logistic related questions with line unit experts.
  • Basic knowledge of drug development.
  • Good organizational skills.

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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