Job Description :
Job Title: Sr. Validation Engineer- Medical Devices
Location: Saint Louis, MO 63143
Duration: 6+ months

Job Title:
Must Have validation experience.

Summary:
The Product Engineer supports the key business objectives of the assigned plant (Growth, Profitability, and Innovation
Through production support and plant specific projects, the associate drives activities to deliver upon these objectives.
Through the execution of deliverables, the Product Engineer is familiar with and capable of performing in many key areas defining the duties and responsibilities of this role

Duties and Responsibilities:
Lead and support process validation activities
Lead and support all aspects of change control projects, including but not limited to: change plan creation, determination and distribution of required assessments, definition of project inputs, and collection of required output evidence.
Assist in the assessment of specifications on products to develop correlation with functional requirements.
Support manufacturing with new designs that will improve the process capability in manufacturing.
Technology transfer: Participate in implementation of transition from research to development to manufacturing.
Work with manufacturing and procurement to identify alternate materials that will meet the quality / functional requirements to replace materials being discontinued, and to reduce raw material cost for current products.
Provide hands on support to all product engineering projects.
Plan, implement, monitor and deliver designated tasks and deliverables
Responsible for solving technical problems.
Accountable for success of assigned tasks and deliverables.
Conduct and facilitate testing to support marketing requirements and claims
Budgeting: Provide input in developing savings project concepts.
Process effectiveness: Ensure appropriate processes are followed for effective and timely engagement of related parties in completion of designated project activities.
Innovation: Develop creative and novel solutions to technical problems.

Knowledge and Skills:
Able to independently organize and prioritize assignments
Demonstrates excellent written and verbal communication skills across all levels.
Process validation experience a must
Experience with design and change control procedures
Experience working in FDA regulated environment a plus
Experience as functional or cross functional liaison with stakeholders concerning project deliverables

Education and Experience Requirements:
Minimum of Bachelors Degree in Engineering (Mechanical or Biomedical preferred)
Minimum of two years experience



Duba koteswari
Technical Recruiter
Direct
Ofc etn: 102
Fax
Email:
Fresno, TX 77545.