A DAY IN THE LIFE:
Serves as the Software Quality Assurance Engineer supporting software product development programs, ensuring software products are developed, validated, and maintained in compliance with applicable quality system and regulatory requirements. Applies knowledge of software lifecycle development, quality processes, and risk management to review development activities, identify quality and compliance risks, and provide guidance on quality best practices. Supports continuous improvement of quality processes to meet department, business unit, and company objectives and serves as the quality representative on cross-functional product development teams.

Sr. Software Quality Assurance Engineers at Tandem are also responsible for:

• Serves as a Quality representative on project core teams and provides quality guidance throughout software development activities.
• Reviews and approves design control deliverables, including requirements, risk management files, verification and validation documentation, traceability records, software change assessments, and design review outputs for compliance with company procedures and regulatory requirements.
• Participates in risk management activities, including identification, evaluation, documentation, and maintenance of product risks, and reviews risk management documentation for compliance with company procedures and applicable standards.
• Provides traceability analysis and reporting to ensure requirements, risks, verification, and validation activities are appropriately linked and documented.
• Provides quality oversight of software anomaly management activities, including review of issue assessments, defect investigations, risk evaluations, unresolved anomalies, and disposition decisions in accordance with company procedures and regulatory requirements.
• Reviews software verification and validation activities and associated test results to ensure requirements are met and documentation is complete and compliant.
• Participates in design reviews and evaluates design review evidence for compliance with company procedures and design control requirements.
• Supports maintenance of the Design and Development File and other development records to ensure completeness, traceability, and compliance.
• Provides quality input to software changes, product releases, and release readiness activities.
• Evaluates and recommends quality-related process improvements, tools, and methodologies.
• Supports Complaint, Field Investigation (FI), Correction and Corrective Action (CA), and CAPA investigations and executes assigned corrective actions when applicable.
• Provides quality support during internal, external, customer, and regulatory audits and inspections.
• Ensures work is performed in compliance with company policies, including Privacy/HIPAA requirements, and applicable regulatory, legal, and safety requirements.
• Supports other departments as needed and considers project-wide impacts in decision making.
• Performs other duties as assigned.

WHEN & WHERE YOU'LL WORK:

This role will be a mix of in-office work at our corporate headquarters in Del Mar, CA and remote work.

WHAT YOU'LL NEED:

• Bachelor's degree in Engineering, Computer Science, Software Engineering, Biomedical Engineering, or a related technical discipline
• Minimum 5 years of experience in software quality assurance, software quality engineering, or related quality functions within the medical device or other regulated industry.
• Experience supporting software development from concept through commercial release.
• Experience with Design Controls, risk management, software verification and validation, and software anomaly management.
• Knowledge of medical device software development processes, including mobile, embedded, and web-based technologies.
• Working knowledge of FDA Quality System Regulation (21 CFR Part 820), ISO 13485, ISO 14971, IEC 62304, and other applicable medical device regulations and standards.
• Working knowledge of Design Controls, risk management, verification and validation, software anomaly management, and traceability principles.
• Familiarity with Good Documentation Practices (GDP).
• Ability to effectively use Microsoft Office applications and other business software tools.
• Excellent written, verbal, and interpersonal communication skills.
• Ability to analyze and interpret technical information and communicate quality and compliance requirements effectively.
• Ability to influence cross-functional teams and facilitate resolution of quality and compliance concerns.
• Demonstrated ability to work independently and manage multiple priorities.

EXTRA AWESOME:

• Experience with application lifecycle management and defect tracking tools preferred.
• Experience with software development languages and technologies such as JavaScript, C, or similar technologies preferred.

COMPENSATION & BENEFITS:

The starting base pay range for this position is $109K - $130K annually. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate's location and the overall job market. In addition to base pay, Tandem offers a competitive compensation package that includes bonus and a robust benefits package.

WHY YOU'LL LOVE WORKING HERE:
At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at https://www.tandemdiabetes.com/careers.

BE YOU, WITH US!

We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don't meet 100% of a job description's criteria - maybe you're feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us.

REFERRALS:
We love a good referral! If you know someone who would be a great fit for this position, please share!

APPLICATION DEADLINE:
The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications.

Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow.

#LI-Remote #LI-KL1