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Document Specialist
Eingestellt von Harvey Nash IT Recruitment Switzerland
Projektbeschreibung
Harvey Nash is looking for an Associate Scientist/Document Specialist for a 6 + month project in Switzerland.
The role is for a documentations specialist for the clients' production documentation to create electronic Master Batch Records in their Manufacturing Executions System as base for the production.
You are responsible for: -Compiling and reviewing GMP compliant manufacturing documentation for clinical supplies in an electronic batch recording system in close collaboration with formulation experts and manufacturing operators.
-Compiling the master batch records based on information provided by our formulation experts and preparing the executed batch records for review by the formulation experts and for approval by quality assurance.
- Contributing to continuous improvement of manufacturing documentation in the newly introduced electronic batch recording system (PAS-X from Werum).
- Taking over other administrative tasks, eg writing of SOPs, writing of cleaning validation assessments.
Requirements
-Pharmaceutical Education (apprenticeship or equivalent)
-Experience in GMP-environment as well as interest in a complex software is of advantage
-The ideal candidate will have a experience in GMP compliant manufacturing documentation and basic knowledge of manufacturing processes for solid dosage forms
-German verbal and written, English language skills are of advantage
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) to (see below) For further details feel free to call me. I am looking forward to receiving your application.
The role is for a documentations specialist for the clients' production documentation to create electronic Master Batch Records in their Manufacturing Executions System as base for the production.
You are responsible for: -Compiling and reviewing GMP compliant manufacturing documentation for clinical supplies in an electronic batch recording system in close collaboration with formulation experts and manufacturing operators.
-Compiling the master batch records based on information provided by our formulation experts and preparing the executed batch records for review by the formulation experts and for approval by quality assurance.
- Contributing to continuous improvement of manufacturing documentation in the newly introduced electronic batch recording system (PAS-X from Werum).
- Taking over other administrative tasks, eg writing of SOPs, writing of cleaning validation assessments.
Requirements
-Pharmaceutical Education (apprenticeship or equivalent)
-Experience in GMP-environment as well as interest in a complex software is of advantage
-The ideal candidate will have a experience in GMP compliant manufacturing documentation and basic knowledge of manufacturing processes for solid dosage forms
-German verbal and written, English language skills are of advantage
Are you available immediately, have experience working within a Life Science company? Please send your complete CV (Word documents preferred) to (see below) For further details feel free to call me. I am looking forward to receiving your application.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges