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Validation Engineer at Remote, Remote, USA
Email: [email protected]
From:

Abhishek singh Golden,

Vyze Inc.

[email protected]

Reply to:   [email protected]

Job Description -

Job Title: 

Validation Engineer

Location: N. Hollywood/Glendale area, Los Angeles(100% onsite)

Open for relocating candidates.

Need 3 managerial references

 attached with the resume. These much each be from different companies. They must be permanent employees of the company your candidate worked for who were signing off on your candidates times sheet. These 

CANNOT

 be another consultant. 

All reference must include: first name, last name, job title, Linkedin, work email address, and work phone number.

Must have P&ID experience.

Must have 1-3 years recent of Validation experience in the pharmaceutical industry 

Must have experience IN THE US.

The 

Validation Engineer

 will be joining a team of around 13 engineers (core team) to execute validation protocols for an expansion project in Los Angeles. This role will be focused on executing validation protocols for equipment including filter presses, centrifuges, and large processing tanks. The facility supports fractionation of blood plasma (closed process so engineers not exposed to plasma).

The client is on a tight timeline right now, they're in the documentation phase so everyone is working 40 hours/week but eventually 24/7 support will be needed from the team so Validation Engineers may be requested to support other shifts. The project will be focused on generating documents until mid-2025, then execution will start. The Validation Engineers on the team will have dedicated equipment assigned to them, but they'll also need to multi-task and support more than one piece of equipment. this project will require strong communication skills to coordinate with cross-functional teams.

The client is on a tight timeline right now, they're in the documentation phase so everyone is working 40 hours/week but eventually 24/7 support will be needed from the team so Validation 

Engineers may be requested to support other shifts. 

The project will be focused on generating documents until mid-2025, then execution will start. The Validation Engineers on the team will have dedicated equipment assigned to them, but they'll also need to multi-task and support more than one piece of equipment. this project will require strong communication skills to coordinate with cross-functional teams.

Top Requirements

:

BS degree minimum

2+ years of Validation Engineering experience in pharmaceutical industry

Strong skill set in installation and IQOQ of equipment like centrifuges, filter presses, and processing tanks

Very strong technical writing/documentation skills

Very strong communication skills and ability to coordinate with cross-functional teams

Experience doing job walks with engineers for capital projects

Must have a positive attitude and ability to multi-task

Regards
,

Abhishek Singh (Golden)
VYZE INC.

Sr. IT Recruiter

Email:  [email protected]

Keywords: information technology Idaho
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Mon Nov 11 20:02:00 UTC 2024

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