Validation Engineer
Company Name:
Career Transitions, LLC
Our client is one of the world's largest contract manufacturers of consumer packaged goods.
This client is looking to hire a Validation Engineer at their Port Washington, WI facility.
The Validation Engineer has the primary responsibility to provide documented evidence through the developments and execution of protocols, the equipment and processes use to manufacture regulated products, meet all the FDA and the company's regulatory requirements.
Job Duties:
Develop and execute installation, operation qualification protocols for processing equipment, utilities, computerized systems and laboratory equipment.
Review and approve change controls
Develop and maintain master validation plan
Perform Training
Project management, track validation progress
Interface with Customers
Perform vendor audits
Requirements:
An Associates or bachelor's degree with a strong emphasis in a natural science.
Must be familiar with regulatory and GMP requirements for pharmaceutical manufacturing operations
Ability to read, analyze, and interpret business information, journals, technical procedures, or governmental regulations.
Excellent communication skills to write reports and findings and present to all levels of management
Strong project management skills
Must maintain good documentation practices
Advanced mathematical concepts such as exponents, logarithms, quadratic equations and permutations
PC proficiency to include Microsoft Office along with Microsoft Outlook, statistical analysis software, contact management software, and the Internet
Estimated Salary: $20 to $28 per hour based on qualifications.
Career Transitions, LLC
Our client is one of the world's largest contract manufacturers of consumer packaged goods.
This client is looking to hire a Validation Engineer at their Port Washington, WI facility.
The Validation Engineer has the primary responsibility to provide documented evidence through the developments and execution of protocols, the equipment and processes use to manufacture regulated products, meet all the FDA and the company's regulatory requirements.
Job Duties:
Develop and execute installation, operation qualification protocols for processing equipment, utilities, computerized systems and laboratory equipment.
Review and approve change controls
Develop and maintain master validation plan
Perform Training
Project management, track validation progress
Interface with Customers
Perform vendor audits
Requirements:
An Associates or bachelor's degree with a strong emphasis in a natural science.
Must be familiar with regulatory and GMP requirements for pharmaceutical manufacturing operations
Ability to read, analyze, and interpret business information, journals, technical procedures, or governmental regulations.
Excellent communication skills to write reports and findings and present to all levels of management
Strong project management skills
Must maintain good documentation practices
Advanced mathematical concepts such as exponents, logarithms, quadratic equations and permutations
PC proficiency to include Microsoft Office along with Microsoft Outlook, statistical analysis software, contact management software, and the Internet
Estimated Salary: $20 to $28 per hour based on qualifications.
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