Validation Engineer
- Contractor
- Full-Time
- Omaha, NE
- Splintpharma
- Prefferd visa: OPT, CPT, H4, Have H1 Visa, Need H1 Visa, EAD
- Posted 1 year ago – Accepting applications
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Offerd Salary $ 40 - $ 52
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Required Position 2-4 hires
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Experience 2-10 Years Required
Validation Engineer
Sr. Validation and Validation Engineer – Omaha, NE
Responsibilities
We are looking for an experienced equipment qualification engineer with experience in a GAMP5 environment to support commissioning of Packaged Equipment (Autoclaves, Parts Washers, WFI Still, etc.) Custom Vessels (Single Use Mixers and bioreactors),and network integration to the Process Control System. Understanding of the execution of Automation IQs and OQs is preferred.
Requirements
• You’ve earned your BS in chemical, biomedical, or biochemical engineering, biological sciences, or related field/experience.
• You’ve gained 2-10 years relevant industry experience working in a cGMP environment., with experience with equipment, process and computer system qualification.
• You’ve got working knowledge of cGMP manufacturing as well as regulatory regulations and requirements for biotechnology, pharmaceuticals, and medical devices in your toolbox.
• You’ve collected previous experience in writing and executing Validation protocols such as Installation, Operation and Performance Qualification documents.
• Experience with enterprise systems.
4-5 months
2 roles
Rate: 40-52 based on experience
Validation Engineer
Sr. Validation and Validation Engineer – Omaha, NE
Responsibilities
We are looking for an experienced equipment qualification engineer with experience in a GAMP5 environment to support commissioning of Packaged Equipment (Autoclaves, Parts Washers, WFI Still, etc.) Custom Vessels (Single Use Mixers and bioreactors),and network integration to the Process Control System. Understanding of the execution of Automation IQs and OQs is preferred.
Requirements
• You’ve earned your BS in chemical, biomedical, or biochemical engineering, biological sciences, or related field/experience.
• You’ve gained 2-10 years relevant industry experience working in a cGMP environment., with experience with equipment, process and computer system qualification.
• You’ve got working knowledge of cGMP manufacturing as well as regulatory regulations and requirements for biotechnology, pharmaceuticals, and medical devices in your toolbox.
• You’ve collected previous experience in writing and executing Validation protocols such as Installation, Operation and Performance Qualification documents.
• Experience with enterprise systems.
4-5 months
2 roles
Rate: 40-52 based on experience