CQV Engineer
- Contractor
- Full-Time
- Bloomington, IN
- Splintpharma
- Prefferd visa: OPT, CPT, F1, H4, Have H1 Visa, Need H1 Visa, EAD
- Posted 1 year ago – Accepting applications
-
Offerd Salary $ 35 - $ 45
-
Required Position 2-4 hires
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Experience 0-3 Years Required
Job Opening for CQV Engineer –Bloomington, IN (onsite)
We currently working on below mentioned job opening i.,e. Job Opening for CQV Engineer –Bloomington, IN (onsite). Please let me know if you are interested in applying for the same.
This assignment requires a candidate to support equipment commissioning in a drug manufacturing environment, with preferred equipment experience to include: single-use mixers, chromatography skids, bioreactors, etc.
Prior CQV experience is preferred, including writing of URS, IOQs, etc
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.
Job Opening for CQV Engineer –Bloomington, IN (onsite)
We currently working on below mentioned job opening i.,e. Job Opening for CQV Engineer –Bloomington, IN (onsite). Please let me know if you are interested in applying for the same.
This assignment requires a candidate to support equipment commissioning in a drug manufacturing environment, with preferred equipment experience to include: single-use mixers, chromatography skids, bioreactors, etc.
Prior CQV experience is preferred, including writing of URS, IOQs, etc
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.