Process validation specialist jobs in United States
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Process Validation Specialist
1 month ago
Only for registered members FargoThe ideal candidate has a strong understanding of the full process validation lifecycle, specifically for biologics products. · Developing Validation Master Plans, · PPQ, · pFMEA Risk Assessments, · ...
- Only for registered members Juncos,
We are seeking a talented dedicated individual committed to work under the highest ethics standards for the following position Validation Specialist. · ...
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Process Validation Specialist
2 weeks ago
Only for registered members FargoWe are searching for a Process Validation Specialist. The ideal candidate has a strong understanding of the full process validation lifecycle, specifically for biologics products. · Strong Understanding of Process Validation Lifecycle · Background in Biologics Products · ...
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Process Validation Specialist
1 month ago
Only for registered members FargoThis company based in Fargo ND is looking for a process validation specialist The ideal candidate has a strong understanding of the full process validation lifecycle specifically for biologics products They will develop validation master plans PPQ pFMEA risk assessments data anal ...
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Process Validation Specialist
2 weeks ago
Only for registered members Caguas Full timeSeeking Process Validation Specialist with experience in ethylene oxide (ETO) sterilization processes to ensure process effectiveness and safety for medical or industrial products. · ...
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Process Validation Specialist
2 weeks ago
Only for registered members Fargo, ND+Our client is searching for a Process Validation Specialist. · +Strong Understanding of Process Validation Lifecycle · Background in Biologics Products (both Drug Substance & Drug Product for API's) · ...
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Process Validation Specialist
2 weeks ago
Only for registered members CaguasWe are looking for a Process Validation Specialist with experience in ethylene oxide (ETO) sterilization processes that comply with applicable regulatory, quality and industry standards to guarantee process effectiveness,reproducibility and safety for medical or industrial produc ...
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Process Validation Specialist
1 day ago
Only for registered members PR-, Caguas, Puerto Rico+Job summary · Process Validation Specialist with experience in ethylene oxide (ETO) sterilization processes comply with applicable regulatory, quality, and industry standards, · +Bachelor Degree Engineering Industrial, Chemical, Biomedical), Microbiology, Sciences or related fie ...
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Process Validation Specialist
2 weeks ago
Only for registered members Caguas, PRProcess validation specialist with experience in ethylene oxide sterilization processes. · ...
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Process Validation Specialist
2 days ago
Only for registered members Caguas, Puerto Rico, , United StatesWe are seeking a Process Validation Specialist with experience in ethylene oxide (ETO) sterilization processes who can guarantee process effectiveness and safety for medical or industrial products. · Develop IQ/OQ/PQ validation protocols for ETO sterilization processes. · Analyze ...
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Process Validation Specialist
2 weeks ago
Only for registered members Caguas Full timeProcess validation specialist with experience in ethylene oxide sterilization processes to guarantee effectiveness and safety for medical or industrial products. · Develop IQ/OQ/PQ validation protocols for EtO sterilization processes. · Conduct load configuration studies, gas pen ...
- Only for registered members Juncos, PR
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: CQV Specialist for Upstream Process Equipment. · Bachelor's degree in engineering, biotechnology or related science field. · 3–7 years of CQV experienc ...
- Only for registered members Humacao, PR
We are seeking a talented individual to join our Validation & Engineering Group as a CQV Specialist for Upstream Process Equipment. · CQV Specialist for Upstream Process Equipment will be responsible for the commissioning and qualification of systems supporting cell culture opera ...
- Only for registered members Gurabo, PR
The CQV Specialist for Upstream Process Equipment will be responsible for the commissioning and qualification of systems supporting cell culture operations in a cGMP biotechnology manufacturing environment. · Author, review, and execute commissioning and qualification protocols ( ...
- Only for registered members Humacao, PR
We are seeking a talented dedicated individual committed to work under the highest ethics standards for the position of CQV Specialist for Upstream Process Equipment. · ResponsibilitiesAuthor review and execute commissioning and qualification protocols (IQ OQ PQ) for upstream equ ...
- Only for registered members Juncos, PR
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · CQV Specialist for Biotech Downstream Process Equipment · ...
- Only for registered members Las Piedras, PR
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · CQV Specialist for Upstream Process Equipment. · ...
- Only for registered members Gurabo, PR
Job summaryWe are seeking a talented dedicated individual committed to work under the highest ethics standards for the following position: · CQV Specialist for Biotech Downstream Process Equipment · ...
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Cleaning Validation Specialist
5 days ago
Only for registered members PR-, Barceloneta, Puerto RicoClean and validate equipment and manufacturing areas. · ...
- Only for registered members Juncos, PR
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Validation Specialist. · ...