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Validation Engineer - All other locations
Ref No.: 18-05924
Location: Rochester, New York
Start Date / End Date: 09/10/2018 to 09/04/2020
kills
Description Level Comments
Negotiation Skills Advanced
Problem Analysis & Resolution Advanced
Process Validation Advanced
Project Management Experience Beginner
Quality Assurance Advanced
Quality Control Advanced
Quality System Compliance Advanced
Quality Systems Regulations Advanced
Software Validation Advanced
System Verification Advanced

Education
Degree Type Major/Certification Required Preferred
Bachelor's Degree active

Job Description & Requirements
Job Type: Recruited Resource - General Temp Number of Positions: 1
System Location: Client - 6118 Created Date: 8/23/2018
Job Title: Validation Engineer - All other locations
CWR Type: W-2 Reason: New Position

Qualifications:
• A minimum of a BA/BS in Life Sciences, Engineering, Physical Science or a related discipline is required; an MA/MS in Life Sciences, Engineering, or Physical Science is preferred. • Must have at least 5 years of related experience in Medical Device quality system management, including experience in working under Design Control. • ASQ certification a plus. • Computer skills/data analysis skills (Word, Excel, PowerPoint, Minitab, Visio, MS Project) is required. • Effective oral & written communication skills are required.

Responsibilities:
• Works independently and sets an example in ensuring compliance to Design Controls and other Quality System requirements to assigned project(s). • Utilizes Six Sigma/Process Excellence to solve complex problems and develop optimal product performance. • Partners with R&D, Operations, Quality, Regulatory and Compliance, suppliers and other groups to ensure effective product development and transfer of knowledge. • Provides technical input as appropriate. • Ensures effective implementation of risk management requirements to prevent unanticipated failure modes and quality issues. • Provides input as needed to regulatory inspections. • Executes Failure Investigations and corrections of design related quality issues. • Utilizes advanced Quality Engineering tools (data analysis, statistics, sampling plans, etc.) to ensure effective product development. • Participates in post-product launch failure investigations. • Provides guidance and leadership to junior members of the team.. • Suppliers/External Manufacturers: Directly or indirectly support design change control activities. • Review and approve plans/protocols and reports, deviations/nonconformances, and document changes through the change control processes for accuracy and completeness. • Proactively identifies issues, troubleshoots issues, and escalates concerns as appropriate. Adheres to strict procedural and quality standards including thorough and accurate documentation, testing protocols.

Comments/Special Instructions


Attached Documentation: No record(s) found.

Work Location: 100 Indigo Creek Drive USRO1, Rochester, NY 14626 United States
Start Date: 9/10/2018 Work Days:
Sun Mon Tue Wed Thu Fri Sat
End Date: 9/4/2020
Start Time: 8:00 AM Total Reg Hours: 40.00
End Time: 5:00 PM Overtime Required:
Lunch Time: 1 Hour