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| Title of job: |
VALIDATION SPECIALIST |
| Job Location: |
Mahwah, New Jersey, 07430 |
| Job Type: |
Contract
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| Price Range: |
| Negotiable, Depending on experience |
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| Start Date: |
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| End Date: |
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| #1 |
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Technical |
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Engineering |
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Bio-Medical |
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| Qualifications: |
1-2 years of of validation experience needed. Applied knowledge of FDA and international medical device regulations required; applied knowledge of the application of Advanced Quality tools, such as Failure Modes Effect Analysis (FMEA), GD&T, SPC, Root Cause Analysis, Mistake Proofing/Poka-Yoke preferred. Demonstrated ability to effectively work cross-functionally with Team Members. Demonstrated problem solving and troubleshooting skills. Demonstrated interpersonal and written communication skills. Positive, energetic team player who is an advocate for product excellence and quality. Demonstrated results orientation, multi-tasker, quick learner; demonstrated ability to respond to urgent needs of the team and deliver expected results within expected deadlines. Applied technical understanding of manufacturing equipment and processes specific to medical device manufacturing. Demonstrated proficiency in standard office software, including Word, Excel, Project, and PowerPoint.
Other desired skills:
VALIDATION SPECIALIST |
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| Job/Project Details: |
Adecco Employment Services is the global leader in employment and HR services, connecting people to jobs and jobs to people through its network of more than 6000 offices in 71 countries and territories around the world. We are currently seeking a Validation Engineer with 1 to 2 years of biomedical industry experience for a medical manufacturingcompany in Mahwah, NJ. This position is responsible for Coordinating multiple equipment validations for loaned biomedical equipment. Responsibilities include revising protocols, executing protocols, and closing protocols. Perform updates, revisions and archiving of the validation documents. Execute the validation of those documents for action of the equipment in the decontamination room. Optimize the Quality System Validation program. Participate in project planning, scheduling, and tracking. Develop and implement procedures to comply with corporate, fda and industry standards. Organize and archive validation documentation. Provide validation training to Operations employees. Mentor support and staff engineersdf-jb |
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