Source description
About the role
Hello Associate,
Hope you are doing well and receiving this email in a high spirit !!
I am urgently hiring for a "Validation Engineer " in New Jersey for one of my esteemed direct clients.
Kindly go through the attached job details and let me know if you have any suitable consultants for the below mentioned position.
Please share your resumes to Sravan@starkassociatesllc.com or contact +1 848-994-4123
Role: Validation Engineer
Work Location: New Jersey
Duration: Long term
Contract
Mandatory Skills:
Must have skills - Good Understanding of FDA (21 CFR Part 210 & 211, 21 CFR Part 11) and GAMP guidelines applicable to computer system validation. Knowledge of HPQC.
Technical proficiency with the Microsoft Office suite of tools required, especially Microsoft Word and Excel is required. Experience with a Validation of GxP applications is required.
Nice to have skills - professional experience in medical devices or pharma computer systems validation OR in computer systems quality assurance (medical device and/or consulting background, excellent verbal and written communication skills.
Pharma/Healthcare industry is preferred.
Duties and responsibilities :
To manage and ensure that the project schedules are adhered to as per the client specifications and deliveries are as per the time and quality standards.
Reports as per the compliance requirements.
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