Equipment Validation Engineer
- Contractor
- Full-Time
- Brookhaven, NY
- Splintpharma
- Prefferd visa: OPT, CPT, F1, H4, Have H1 Visa, Need H1 Visa, EAD
- Posted 1 year ago – Accepting applications
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Offerd Salary $ 35 - $ 40
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Required Position 2-4 hires
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Experience 0-3 Years Required
Job Opening for Equipment Validation Engineer, Brookhaven, NY – on site
We are currently working on below mentioned job opening i.e., Job Opening for Equipment Validation Engineer, Brookhaven, NY – on site. Please let me know if you are interested in applying for the same.
Brookhaven, NY – on site
2 + year project
Project description: Client has transferred Equipment from another site to Brookhaven, New York facility and has existing Manufacturing /Packaging, Utilities Equipment that needs to be re-Validated. There are existing Protocols, Templates, SOP’s but these engineers will need to perform IQ, OQ, PQ, change controls, CAPA, Deviations and may write new or edit SOPs as necessary.
Work is in 21CFR /GMP/Oral Solid Environment
Equipment includes compressors, tablet sorters, coating, track and place, utilities vacuum systems, clean steam, compressed air.
Consultant’s day to day responsibilities
Review SOP’s and determine if they need to be modified or re-written
Write /Edit SOP’s
Perform IQ, OQ, PQ, change controls, CAPA, Deviations on new and existing Manufacturing /Packaging Equipment
Follow appropriate guidelines for 21 CFR /GMP environment
Must be Vaccinated for COVID 19
Required skills:
BS in Engineering
Experience as Validation Engineer writing /editing SOPs for Mfg. Equipment within 21CFR/GMP/Oral Solid Environment
Experience performing IQ, OQ, PQ, change controls, CAPA, Deviations Manufacturing /Packaging Equipment
Must be Vaccinated for COVID 19
Job Opening for Equipment Validation Engineer, Brookhaven, NY – on site
We are currently working on below mentioned job opening i.e., Job Opening for Equipment Validation Engineer, Brookhaven, NY – on site. Please let me know if you are interested in applying for the same.
Brookhaven, NY – on site
2 + year project
Project description: Client has transferred Equipment from another site to Brookhaven, New York facility and has existing Manufacturing /Packaging, Utilities Equipment that needs to be re-Validated. There are existing Protocols, Templates, SOP’s but these engineers will need to perform IQ, OQ, PQ, change controls, CAPA, Deviations and may write new or edit SOPs as necessary.
Work is in 21CFR /GMP/Oral Solid Environment
Equipment includes compressors, tablet sorters, coating, track and place, utilities vacuum systems, clean steam, compressed air.
Consultant’s day to day responsibilities
Review SOP’s and determine if they need to be modified or re-written
Write /Edit SOP’s
Perform IQ, OQ, PQ, change controls, CAPA, Deviations on new and existing Manufacturing /Packaging Equipment
Follow appropriate guidelines for 21 CFR /GMP environment
Must be Vaccinated for COVID 19
Required skills:
BS in Engineering
Experience as Validation Engineer writing /editing SOPs for Mfg. Equipment within 21CFR/GMP/Oral Solid Environment
Experience performing IQ, OQ, PQ, change controls, CAPA, Deviations Manufacturing /Packaging Equipment
Must be Vaccinated for COVID 19