Validation Engineer

E-CQR is a San Diego based company and offers a broad range of business solutions and technology services to help clients in achieving their business goals. Our top notch consultants are providing services to industry's top Pharmaceutical, Biotechnology, Medical device, Clinical research, Diagnostics, Chemical, Bio Medical, Drug development, Bioinformatics and Therapeutics companies.

We are looking for a Junior to Mid Level Validation Engineers to support our clients in USA and also open for relocation.

Responsibilities:

• Provide CSV authoring, review and approval of validation documents developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards.
• Initiate/update GxP and Risk Assessments on system.
• Author, Review and or approve scheduled periodic reviews.
• Author, Initiate, and/or review and approve IT SOPs related to compliance
• Collaborate with project stakeholders and the information systems team to define needs and achievable solutions and/or justifications to system requirements
• Provide support to executors of the protocols when needed
• Write reports summarizing system validation

Requirements:                                                                                                                                                  

• Bachelors / Masters Degree in any Engineering
• Must have strong written and verbal communication skills
• Looking for the candidates who are authorized to work in USA( OPT, GC, EAD and Citizen)

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