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15835en
- Contract
- English
- Associate
- Research & Development
- Bern
- Healthcare & Life Sciences
Skills
QC, Gene Therapy, cGMP, GMP, QC Testing
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This vacancy has now expired
On behalf of our client, an international Biotechnology company based in Bern, we are now seeking a Quality Control Analyst.
Start Date: 5th of May
Location: Bern
Workload: 100%
Work Type: Hybrid
Duration: 12 months (with possible extension)
Your mission:
- Provide independent verification and review and/or approval of data and reports generated to support the development, validation,
and analytical lifecycle management of gene therapy methods
- Prepare, review and update standard operating procedures, test procedures and protocols
- Manage the development of project plans including estimated cost, time and resources for the identified work activities
- Independently develop and execute appropriate testing and experimental plans
- Lead the development, qualification, validation and transfer of methods between R&D, QC and external laboratories as required.
Your background:
- Degree in Engineering, Physical, or Biological Science or equivalent
- A minimum of 3 years’ experience in cGMP Quality Control and at least 2 years’ experience in method development for assessment of gene therapy products
- Experience in method development and validation for testing of AAV or similar products for gene therapy suitable for cGMP application
- Experience in cGMP testing, with experience in the QC testing of gene therapy products a plus
- Proven written and verbal communication skills
- Experience in all aspects of analytical method lifecycle management
What’s an offer?
You get to be part of a dynamic work environment where your expertise is valued!
Start Date: 5th of May
Location: Bern
Workload: 100%
Work Type: Hybrid
Duration: 12 months (with possible extension)
Your mission:
- Provide independent verification and review and/or approval of data and reports generated to support the development, validation,
and analytical lifecycle management of gene therapy methods
- Prepare, review and update standard operating procedures, test procedures and protocols
- Manage the development of project plans including estimated cost, time and resources for the identified work activities
- Independently develop and execute appropriate testing and experimental plans
- Lead the development, qualification, validation and transfer of methods between R&D, QC and external laboratories as required.
Your background:
- Degree in Engineering, Physical, or Biological Science or equivalent
- A minimum of 3 years’ experience in cGMP Quality Control and at least 2 years’ experience in method development for assessment of gene therapy products
- Experience in method development and validation for testing of AAV or similar products for gene therapy suitable for cGMP application
- Experience in cGMP testing, with experience in the QC testing of gene therapy products a plus
- Proven written and verbal communication skills
- Experience in all aspects of analytical method lifecycle management
What’s an offer?
You get to be part of a dynamic work environment where your expertise is valued!
I manage this role