Job Description :
Company Overview:

Creating value by bringing together the right people to achieve results is our motto. Our clients and employees say they choose to work with us because of how we work with them - with service that exceeds their expectations and a personal commitment to their success.

Our client, a leading developer, manufacturer and marketer of integrated systems for analysis of genetic variation and biological functions and serving customers at genomic research centers, clinical research organizations, biotechnology & pharmaceutical companies, seeks an accomplished Supplier Development QE.

Participate as a core member of development teams to assure processes are in place to design and release highly reliable products.
Provides Quality Assurance expertise and guidance for New Product Development, Manufacturing Operations, Supplier Development, and Product Quality.
Aides in the assessment and qualification of new supplier materials such as component specifications and inspection standards.
Maintain goals and metrics for existing and new products, regularly reporting on the progress to reach product objectives.
Participates in supplier audits to drive process standardization and continuous improvement.
Identify opportunities for reduced inspection of purchased materials based on risk and quality performance.
Leads and facilitates failure investigations; ensuring mitigations and corrective actions are implemented in a timely manner.
Contribute and lead component qualification deliverables such as process validation, first article inspection, and capability studies.
Works with strategic partners and suppliers to ensure global awareness and compliance to procedures and specifications.

BS or equivalent in a technical discipline with 5+ years of experience.
MS or PhD in a technical discipline with 3+ years of experience.
Experience working in a regulated environment, in-vitro diagnostics preferred.
Experience contributing to cross-functional product development teams.
Experience with Quality, Project Management, and Process Engineering methodologies and tools.
Demonstrated capability in successfully managing and leading change.
Practice identifying, mitigating, and resolving risks.
Ability to work effectively in a fast-paced, dynamic environment with shifting and competing priorities.
Exceptional communication skills, both written and verbal, including executive presentations.
Demonstrated experience with data analysis, value stream mapping, 6-Sigma, and Kaizen events preferred.
Extensive experience with Microsoft Office (Words, Excel, PowerPoint
Experience with electronic product life cycle (PLM) systems such as Agile or SAP.
Practical experience in FDA and ISO regulated environments is a plus.
Experience with statistical analysis packages such as JMP and Minitab is a plus.
Ability to travel as needed.

I''d love to talk to you if you think this position is right up your alley.

If you''re looking for rewarding employment and a company that puts its employees first, we''d like to work with you. We''re driven, people driven. We also offer group health Insurance (employee paid on a pre-tax basis

NOTE: “Candidates that are offered a position are required to pass pre-employment drug and background screening”