Quality Engineer II

Duration: 12 months contract Job Description: Ensure compliance to new and changing regulations affecting products and processes including, but not limited to, QSR’s, global import/export regulations, etc.

New product setup and management of related projects Assist with Supplier audits, as needed Maintenance of BSE Serum Certificates of Suitability filing with EDQM Collaborates with USDA on regulatory compliance activities including regulatory approvals, import/export compliance, traceability, quarantine, safety testing and affidavits. Serve as a resource for customer’s regulatory and technical inquiries Ongoing maintenance of ISO 13485 based quality system Implement and handle CAPA (Corrective and Preventive Actions) and problem resolution. Coordinates and leads Quality Documentation, Nonconformance Reports, Inspection Activities, and Product Disposition.

Coordinates the review and revision of procedures, specifications, and forms to maintain and improve the QMS. Quality Help Desk and customer complaint point of contact and problem resolution including Questionnaires, Certificates and Customer Surveys, etc. Perform Internal Audits in support of internal requirements, 21 CFR 820 and ISO 13485 compliance.

Assists in representing in customer quality audits, supplier quality audits and regulatory inspections Performs investigations and analysis activities to support resolution of quality issues. Collaborates with organizational teams to support quality system implementation. Creation of new product master files satisfying customer and quality system requirements Ensures quality standards by following company & departmental policies & procedures including, but not limited to Product performance & quality verification.

Identifying, recording, and investigating problems related to product, process & quality systems. Evaluating processes for improvements and standardization. Initiating action to prevent non-conformance in products, process, and quality systems.

Training on quality systems and applicable regulations as identified by supervisor and required by position. Tracking/trending aspects of the QMS. Other job duties as required Experience:

Minimum 3 years’ experience in Quality or Regulatory, preferably in a medical device, pharmaceutical or biotechnology environment/industry. Skills: Thorough knowledge and practical application of Quality Systems Regulations 21 CFR 820 and ISO 13485 Ability to develop, update and train on SOPs. Working knowledge of ISO standards and Quality Management Systems (QMS). Problem solving techniques to perform investigations and drive root cause analysis.

Related work experience performing internal/external audits. Ability to monitor the QMS such as: Change Control, CAPA, Complaints, Nonconforming Materials and Products.

Experience with Continuous Improvement, Lean or Six Sigma. Desired Experience / Qualifications / Skills: SAP, EtQ and/or PeopleSoft experience.

Experience with statistical analysis. Project management experience. Animal by-product import/export regulations Animal health and/or virology, immunology, epidemiology knowledge Education:

Minimum of Bachelor’s degree in Chemistry or Biology degree programs. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions.

To know more about US Tech Solutions, please visit www.ustechsolutions.com. US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Recruiter Details: Name: Ashwini Email: ashwini.sustechsolutionsinc.com Internal Id: 24-17797