Agilent Technologies is seeking a Validation Engineer to oversee qualification and validation activities at their API manufacturing sites. The role involves generating and reviewing validation documentation, ensuring compliance with regulatory standards, and contributing to continuous improvement efforts in validation processes
Job Summary
The role involves executing all qualification and validation activities excluding process validation at Agilent's Active Pharmaceutical Ingredient manufacturing sites.
Candidates must generate and review comprehensive validation documentation including plans, protocols, and reports while ensuring strict adherence to cGMP requirements.
The position offers a competitive salary range of $103,200.00 - $161,250.00 per year plus eligibility for bonus, stock, and benefits.
Matching Summary
Match Score: 85
Agilent Technologies is seeking a Validation Engineer to oversee qualification and validation activities at their API manufacturing sites. The role involves generating and reviewing validation documentation, ensuring compliance with regulatory standards, and contributing to continuous improvement efforts in validation processes.
Salary
Base: $103,200.00 - $161,250.00/yr; Bonus/Equity: Eligible for bonus and stock; Benefits: Eligible for benefits
Skills & Requirements
Must-have
cGMP regulatory compliance knowledge
validation protocol generation and execution
21 CFR and ICH Q7 regulation expertise
equipment and computerized system validation
CAPA and change control management
Nice-to-have
strong written communication skills
ability to work in fast-paced team environment
experience with statistical analysis tools
subject matter expert for client audits
high attention to detail and ethical standards
Key Requirements
Bachelor's degree in engineering or life sciences
Minimum 4 years of validation related experience
Proficiency with MS Word, Excel, and statistical tools