The Complaint Analyst, Post Market Quality is responsible for maintaining customer-facing and field activities including complaint handling and product investigations activities, coordinating Quality System / Regulatory Compliance (QS/RC) interactions, requirements and compliance activities interfacing with Technical Service, Technical Support and other customer support teams, and executing Quality Systems and Regulatory Compliance requirements in conjunction with Company, Business and Regulatory requirements.  You will have growth opportunities within Post Market Quality, and other Quality related functions.

This position is part of the Post Market Quality team and will be hybrid with expectation to be on site three days per week in Sunnyvale, CA. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions.

In this role, you will have the opportunity to:

• Support integration of the Post Market Process into all facets of the QMS to include management controls, Complaint Handling, Corrective and Preventive Actions, and Risk Management.
• Support processing Customer Complaints in a compliant and timely manner.
• Interface with Technical Support to manage, track, and address complaint rejections.
• Support changes to QS/RC processes through timely analysis and completion of field reports, service requests and customer complaints.
• Continuously review requirements and practices in customer-facing responsibilities to ensure compliance to business, customer, and regulatory needs.

The essential requirements of the job include:

• Bachelor’s degree with 0-2 years of related work experience
• Possess essential skills for self-directed manner, prioritizing workload and responsibilities.
• Strong written communication, interpersonal, negotiations and problem-solving skills.
• Team player.

It would be a plus if you also possess previous experience in:

• Post Market Surveillance requirements
• Using Salesforce
• Functional knowledge of Quality, Regulatory Compliance, and operations systems and processes to include GMP and QSR requirements for medical devices. (ISO 13485, FDA’s QSRs, EU’s MDD, Canadian Regulations) is required.

Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.

At Cepheid we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part of the time at the Company location identified above and part of the time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cepheid can provide.

The salary range for this role is $72,600 – 92,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

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