Validation Engineering Consultant (Onsite)
- Contractor
- Full-Time
- NC
- Splintpharma
- Prefferd visa: OPT, CPT, F1, H4, L2, Have H1 Visa, Need H1 Visa, EAD, TN Permit Holder
- Posted 3 years ago – Accepting applications
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Offerd Salary $ 25 - $ 45
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Required Position 2-4 hires
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Experience 0-3 Years Required
Job Opening for Validation Engineering Consultant (Onsite), NC . Please let me know if you are interested in applying for the same. Validation Engineering Consultant (Onsite)
This is a 6 month onsite assignment with potential for extension based on performance.
Assignment Overview: Our client is a leading biopharmaceutical manufacturer who is currently in the process of ramping up their manufacturing plants on the East Coast. They currently need a validation engineering consultants to support them as an array of new equipment and process validation.
This consultant will be responsible for working closely with the client’s validation, manufacturing, and quality engineering teams to ensure that all commissioning, qualification, and validation activities are completed correctly.
These consultants should be well-versed in equipment and process validation for upstream and downstream pharmaceutical manufacturing equipment. The ideal consultants will be responsible for both the development and execution of validation protocols.
This project will give our consultants an opportunity to support an exciting expansion for one of the industry’s leading pharmaceutical manufacturers, ultimately ensuring that the company can manufacture and distribute life-saving Covid therapies to patients around the world.
Job Opening for Validation Engineering Consultant (Onsite), NC . Please let me know if you are interested in applying for the same. Validation Engineering Consultant (Onsite)
This is a 6 month onsite assignment with potential for extension based on performance.
Assignment Overview: Our client is a leading biopharmaceutical manufacturer who is currently in the process of ramping up their manufacturing plants on the East Coast. They currently need a validation engineering consultants to support them as an array of new equipment and process validation.
This consultant will be responsible for working closely with the client’s validation, manufacturing, and quality engineering teams to ensure that all commissioning, qualification, and validation activities are completed correctly.
These consultants should be well-versed in equipment and process validation for upstream and downstream pharmaceutical manufacturing equipment. The ideal consultants will be responsible for both the development and execution of validation protocols.
This project will give our consultants an opportunity to support an exciting expansion for one of the industry’s leading pharmaceutical manufacturers, ultimately ensuring that the company can manufacture and distribute life-saving Covid therapies to patients around the world.