- - Review/implementation of QMS
- Ensure GMP & GLP compliance and documentation
- Handling of deviations, change controls, non-conformances
- Manage critical quality parameters
- Develop effective mechanism for investigations and analytics
- Conduct GMP audits
- Coordination with other functions and regulatory auditors
- Contribute in solving queries from regulatory authorities
Qualifications:
M.S. in Analytical Chemistry, Chemistry, Microbiology, Pharmaceutical Sciences or equivalent with multiple years of pharmaceutical experience
Understanding of pharmaceutical manufacturing and packaging operations of large volume parenterals
We are looking for an effective and team-oriented leader with hands-on experience in controlling QA, QC chemistry and QC Microbiology
Experience in
- Quality Management System
- Large Volume Parenterals
- developing SOPs, protocols and technical documents
- Deviation management and batch disposition
- Validation and qualification activities
- Auditing and authority inspections
- Experience in QC Microbiology is preferable
M.S. in Analytical Chemistry, Chemistry, Microbiology, Pharmaceutical Sciences or equivalent with multiple years of pharmaceutical experience
Understanding of pharmaceutical manufacturing and packaging operations of large volume parenterals
We are looking for an effective and team-oriented leader with hands-on experience in controlling QA, QC chemistry and QC Microbiology
Experience in
- Quality Management System
- Large Volume Parenterals
- developing SOPs, protocols and technical documents
- Deviation management and batch disposition
- Validation and qualification activities
- Auditing and authority inspections
- Experience in QC Microbiology is preferable
10+ years experience
Recruiter Name:Fredrik
Company:DoPharma
Email Address:frederic.dovi-akue@dopharma.net
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