Analista de Garantia de Qualidade - Sao Paulo, Brasil - MSD
Descrição
Main responsibilities include, but are not limited to:
- Preparation of Standard Operating Procedure (SOP's), Review and Approval;
- Preparation, Review and Approval of Raw Material Specifications;
- Preparation, Review and Approval of Packaging Material Specifications;
- Preparation, Review and Approval of Finished Product Specifications;
- Change Control;
- Deviation and Complaint Investigation;
- Investigation of Out of Specification Results;
- Preparation, Review and Approval of Batch Records;
- Batch Records Reconciliation and Artworks Review;
- Documentation Control and Archive;
- Review of Certificate of analysis including raw data verification;
- Stability Studies.
Mais requirements:
- Bachelor's degree in Industrial Chemistry, Pharmacy or Chemical Engineering;
- Previous exerience in the Quality Area in a Pharmaceutical company;
- Experience in Microsoft Office (Word, Excel, Power Point and Outlook)
- Knowledge in technology transfer in third party manufacturing
- Strongly knowledge in the Good Manufacturing Practice and Good Laboratory Practices
- Knowledge in the MAPA Requirements for Veterinarian Pharmaceutical Products including stability data.
Search Firm Representatives Please Read Carefully
Employee Status:
Project Temps (Fixed Term)
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
No Travel Required
Flexible Work Arrangements:
Hybrid
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
N/A
Requisition ID:
R291357
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