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You will be updated with latest job alerts via emailJob Summary:
The Validation Engineer is responsible for executing and documenting equipment and process validations (IQ OQ PQ) on various types of manufacturing equipment and end-of-line processes. This role involves interfacing with clients regarding all qualification details technical issues and supporting project deliverables. Depending on the level of the position the Validation Engineer may lead QA projects of moderate scope and duration or independently perform detailed engineering tasks.
Essential Duties and Responsibilities:
Bachelors Engineering Degree (optional): Mechanical biomedical chemical industrial plastics materials etc.
Experience in medium/high volume Medical Pharmaceutical Industry is highly desirable.
Design Assurance: 2-5 years.
Test Method Development: 2-5 years.
Med-tech New Product Development: 2-5 years
Generate test protocols: 2-5 years.
Technical Report Writing: 2-5 years.
Plastics IM EBM ISBM & IBM experience is desirable.
Excellent verbal and written communication skills including the ability to contribute technically to and work within cross-functional team environments.
High personal/professional integrity trustworthiness strong work ethic and ability to work independently.
Ability to work in a dynamic and collaborative environment and maintain a results-oriented positive can-do attitude and ability to work well under pressure.
Strong organizational and multitasking skills with a high level of attention to detail and a proactive approach to problem-solving.
Ability to read analyze and interpret technical procedures or government regulations.
Ability to write reports correspondence and procedure manuals. Ability to effectively present information and respond to questions from groups of department heads managers and clients.
Proficiency in Microsoft Office Suite (Outlook Word Excel PowerPoint Minitab).
Standard Health Dental Vision Benefits.
Generous PTO.
401K Match.
Full-Time