Supplier Quality Associate II Position Available In Orleans, New York

Supplier Quality Associate

II 4.5 4.5

out of 5 stars Medina, NY 14103 Primary Talent Partners has a 6 month contract opening for a Supplier Quality Associate II to join a multinational medical device company for an onsite position operating out of Medina, NY.

Pay:

$36.00/hr – $41.00/hr

Contract:

6 months, extensions likely, conversion possible

Type:

W-2, cannot support C2C or provide visa sponsorship

Responsibilities:

Develop and communicate expectations for quality performance, continuous improvement, quality systems, and process controls for both critical sustaining parts and new products. As required, participate as an active member in the new products development team.

Perform and coordinate supplier:

surveys, quality system, and process control assessments. Work with purchasing to measure and communicate supplier performance on key metrics and the corresponding continuous improvement plans. Collaborate with supplier representatives in establishing effective quality systems, process controls, and problem-solving methodologies. Conduct process and component validations as applicable. Monitor and drive corrective action and continuous improvement activities that directly impact performance for assigned suppliers. Conduct or lead event investigations and root cause analyses relative to purchased materials and components. Perform other duties as assigned.

Qualifications:

Bachelor’s Degree required. Lead Auditor training, ISO Lead Assessor training, with 1-2 years’ experience in auditing techniques, interpreting regulations and quality systems. Minimum of 3-5 years of experience in Quality, or related field in the medical products industry. Knowledge & application of reading and understanding blueprints/technical drawings. Display a solid understanding of theories/practices utilized by other disciplines outside primary area of expertise. Experience in manufacturing/quality assurance engineering in an FDA regulated environment. Knowledge and working application of standard operating procedures. Knowledge and working application of FDA cGMP;

ANSI/ISO/ASQC

; CMDAS requirements. Knowledge and working application of data entry and spreadsheet applications. Computer competency in Word, Excel, Power Point, Minitab, Access and databases. Practical experience in metrology, test equipment, inspection and analysis techniques. Desired experience is in the medical device industry development and deployment of Quality System and process controls and continuous improvement methods (QSR, ISO13485). Desired CQE, CSSBB, CQA or initiative to complete certifications. Primary/Secondary party compliance auditing experience. Ability to multi-task and methodically manage projects Ability to convince management on courses of action with minimal assistance using both written and verbal methods. Effectively operate in and facilitate cross-functional teams with guidance. Must be able to provide solutions that reflect understanding business objectives and cost implications.

Ability to:

stand or walk for long periods, lift and carry at least 20 pounds, perform repetitive motions with hands/fingers. Demonstrated strong analytical problem solving (CAPA), teaming, and communications/interpersonal skills. Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws. If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at info@primarytalentpartners.com #PTPJobs #LI-PTP