CQV Engineer
- Contractor
- Full-Time
- NJ
- Splintpharma
- Prefferd visa: OPT, CPT, F1, H4, Have H1 Visa, Need H1 Visa, EAD
- Posted 1 year ago – Accepting applications
-
Offerd Salary $ 25 - $ 40
-
Required Position 2-4 hires
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Experience 0-3 Years Required
Job Opening for CQV Engineer, NJ, Client: Novartis
We are currently working on below mentioned i., e. Job Opening for CQV Engineer, NJ, Client: Novartis. Please let me know if you are interested in applying for the same.
Looking for 3-4 engineering resources within Manufacturing.said high volume.10-15 years of experience.onsite 5 days a week.MMD Project.mentioned isolators, blast phaser
BSL 2 Isolators
Large scale lyophilizer experience
10-15 yrs experience
Someone like Sri would be great if he could be onsite.
Our other opportunity is to seek 3 candidates to be onsite in Morris Plains NJ for at least 4 months, possible longer.
Candidates must have experience with authoring and executing Commissioning/Qualification protocols, including summary reports and performing root cause analysis for protocol deviations. Ideal candidates will have strong organization, communication, good documentation practices, technical writing and problem-solving skills, and are driven to complete projects in a timely fashion. They should have experience working effectively as part of a cross functional team including QA. They should have experience with leveraging commissioning for qualification (enhanced commissioning). Candidates should have a minimum 5 years of C&Q experience within a GMP regulated environment, experience with equipment utilized in Cell and Gene Therapies manufacturing and testing is preferred, but not required.
These individuals should possess the following competencies and experience outlined below:
• Qualification of classified Cleanrooms (ISO 5, ISO 7, and ISO 8)
• Qualification of manufacturing/laboratory equipment (including 21 CFR Part 11 in addition to temperature mapping of chambers)
• Commissioning and qualification of clean utilities (compressed process air and CO2).
Job Opening for CQV Engineer, NJ, Client: Novartis
We are currently working on below mentioned i., e. Job Opening for CQV Engineer, NJ, Client: Novartis. Please let me know if you are interested in applying for the same.
Looking for 3-4 engineering resources within Manufacturing.said high volume.10-15 years of experience.onsite 5 days a week.MMD Project.mentioned isolators, blast phaser
BSL 2 Isolators
Large scale lyophilizer experience
10-15 yrs experience
Someone like Sri would be great if he could be onsite.
Our other opportunity is to seek 3 candidates to be onsite in Morris Plains NJ for at least 4 months, possible longer.
Candidates must have experience with authoring and executing Commissioning/Qualification protocols, including summary reports and performing root cause analysis for protocol deviations. Ideal candidates will have strong organization, communication, good documentation practices, technical writing and problem-solving skills, and are driven to complete projects in a timely fashion. They should have experience working effectively as part of a cross functional team including QA. They should have experience with leveraging commissioning for qualification (enhanced commissioning). Candidates should have a minimum 5 years of C&Q experience within a GMP regulated environment, experience with equipment utilized in Cell and Gene Therapies manufacturing and testing is preferred, but not required.
These individuals should possess the following competencies and experience outlined below:
• Qualification of classified Cleanrooms (ISO 5, ISO 7, and ISO 8)
• Qualification of manufacturing/laboratory equipment (including 21 CFR Part 11 in addition to temperature mapping of chambers)
• Commissioning and qualification of clean utilities (compressed process air and CO2).