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Supplier Quality Engineer

Who We Are

Frida is more than a brand built to support parents. We get parents. We know all about the often unbelievable realities of parenthood, because we’ve been in the trenches. Over the last 9 years, we’ve dedicated ourselves to developing the tools (and sometimes the tips, too) that help simplify parenting - and it all started with snot. Since the launch of our cult-favorite NoseFrida, The SnotSucker, we’ve innovated and launched over 100 products that provide quick and easy solutions to age-old parenting problems. We also launched Frida Mom in 2019, with products to help women with the transition through the fourth trimester into motherhood. Today, Frida holds over a 70% share of its main category, and our products can be found in over 50+ countries and in over 40,000 stores throughout the US - in every retail channel from mass-market, grocery, chain drug, and specialty stores. For 9 years, we’ve had parents’ backs as they navigate the parts of parenthood you don’t usually see on the ’gram with honest and raw messaging to provide the answers to questions they didn’t even know they had. And, we’re just getting started.

How You Will Make an Impact

Frida is looking for a Supplier Quality Engineer to join our Operations team to take the lead in managing our critical supplier relationships and ensuring the quality and compliance of all our products. In this pivotal role, you will serve as the primary quality interface between Frida and our supplier network, leading qualification processes, conducting risk assessments and audits, investigating quality issues, and driving continuous improvement initiatives—all while ensuring strict adherence to FDA regulations, ISO 13485 and international standards. The ideal candidate combines technical expertise with strong relationship management skills to maintain our high standards of product quality and safety. 

Responsibilities to include:

  • Supplier Qualification & Management
    • Lead the qualification process for new suppliers, conducting risk assessments, capability evaluations, and quality system audits.
    • Develop and maintain the Approved Supplier List (ASL) based on performance, compliance, and risk analysis.
    • Collaborate with procurement and R&D to ensure suppliers meet technical and regulatory requirements.
    • Establish and monitor supplier Key Performance Indicators (KPIs), such as defect rates and compliance metrics.
  • Supplier Audits & Compliance
    • Plan, execute, and document supplier audits in compliance with FDA, ISO 13485, and internal quality requirements.
    • Ensure suppliers implement corrective and preventive actions (CAPAs) for any non-conformances identified during audits.
    • Maintain supplier audit schedules and track follow-up activities to ensure timely resolution of findings.
  • Supplier Issue Management & Continuous Improvement
    • Investigate supplier-related quality issues, including non-conforming materials, component failures, and deviations.
    • Work closely with suppliers to implement process improvements, reduce defects, and enhance product reliability.
  • Regulatory Compliance & Documentation
    • Ensure supplier documentation, such as Certificates of Compliance (CoC) and process validations, meet regulatory requirements.
    • Maintain supplier-related quality records in compliance with ISO 13485, and other relevant standards.
    • Support regulatory and customer audits by providing supplier-related quality documentation and evidence of compliance.
  • Cross-Functional Collaboration
    • Partner with Operations, Engineering, and Procurement teams to resolve supplier-related manufacturing issues.
    • Participate in Design Review meetings to provide input on supplier capabilities and constraints.
    • Support complaint investigations related to supplier components and materials.

What You Will Need

  • Bachelor's degree in Engineering, Quality, or related technical field.
  • 4+ years of experience in supplier quality within the medical device industry.
  • Thorough knowledge of FDA regulations, ISO 13485, and medical device quality systems.
  • Certified quality professional (CQE, CQA, or equivalent) preferred.
  • Experience with risk management methodologies (FMEA, FTA) and statistical process control.
  • A keen eye for detail and a results-driven approach
  • Strong auditing skills with demonstrated ability to identify and resolve quality issues.
  • Excellent verbal communication skills with ability to speak effectively with clients, vendors, management staff and employees of organization
  • Working knowledge of Microsoft Excel, Word, Access, Visio, and documentation control software (preferably Aras PLM), material management software, and statistical application software 
  • Willingness to travel (approximately 20-30%) for supplier audits and assessments.

Who You Will Work With

Frida is an organization that values collaboration and community. As the Supplier Quality Engineer, you will work closely with Operations, Engineering, and Procurement teams. 

Our Ways of Working

Frida HQ is located in Miami, Florida and approved roles have the flexible option to work remotely both Mondays and Fridays with the benefit of connecting in person Tuesdays - Thursdays.

Why You Will Love Working at Frida

  • Robust health benefits including:
    • Comprehensive medical, vision, and dental plans
    • Employer paid life insurance
    • Supplemental insurance options including Accident Insurance, Short-Term Disability and Long-Term Disability 
    • FSA & HSA
  • 401k matching up to 4% with immediate vesting.
  • Generous paid time off program including elective PTO days, federal holidays, sick/wellness days, and a birthday floater.
  • Flexible paid pregnancy and parental leave.
  • Weekly wellness programming designed to maximize personal time and minimize time spent investing in personal care outside of work hours. This includes a variety of programming such as in-office manicures & pedicures, blowouts, massages, and carwash services.
  • Dog friendly office - feel free to bring your best buddy with you to work! 
  • Learning & development opportunities for professional and personal growth
  • Company-wide events & outings. Team engagement is at the center of our culture. This ranges from small department-specific teambuilding or informal outings to our annual Fam Jam family carnival that celebrates the people in your life who support you in bringing your best self to work each day. We also host an annual Day of Service to support our local Miami community, and provide a variety of volunteer opportunities throughout the year that support our mission to serve parents and children.
  • Exclusive employee product discounts.

Frida provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected Veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

By applying for this position, you acknowledge and understand that your information will be used as described in Frida's Job Applicant Privacy Policy: https://frida.com/pages/fridababy-job-applicant-privacy-policy

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What You Should Know About Supplier Quality Engineer, Frida

Frida is seeking a talented Supplier Quality Engineer to enhance our Operations team. At Frida, we know the challenges of parenthood and aim to provide innovative solutions, and this role is pivotal in maintaining the high quality and compliance of our beloved products. In this position, you'll be the main quality liaison between Frida and our supplier network, taking charge of supplier qualifications, conducting thorough risk assessments, and leading audits to ensure our products meet strict FDA regulations and ISO 13485 standards. Your day-to-day will involve developing and maintaining our Approved Supplier List, collaborating with procurement and R&D to ensure adherence to technical and regulatory needs, and establishing Key Performance Indicators to track supplier performance. As a Supplier Quality Engineer at Frida, you’ll not only address quality issues as they arise, but also champion continuous improvement initiatives with our suppliers. This is an opportunity to immerse yourself in the medical device industry with a focus on quality and safety while making a direct impact on the lives of parents everywhere. So, if you have a Bachelor’s degree in Engineering or Quality, 4+ years of relevant experience, and possess strong communication and auditing skills, we can’t wait to meet you! Join us in this rewarding journey where you’ll play a crucial role in ensuring the exceptional quality of our innovative parenting products!

Frequently Asked Questions (FAQs) for Supplier Quality Engineer Role at Frida
What are the main responsibilities of the Supplier Quality Engineer at Frida?

As a Supplier Quality Engineer at Frida, you'll lead the qualification process for new suppliers, conduct risk assessments and audits, and maintain compliance with FDA regulations and ISO 13485. Your role also involves managing supplier relationships to ensure product quality, tracking Key Performance Indicators, and implementing corrective actions for any quality issues that arise.

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What qualifications are needed to be a Supplier Quality Engineer at Frida?

To be successful as a Supplier Quality Engineer at Frida, candidates should have a Bachelor's degree in Engineering, Quality, or a related field, along with at least 4 years of experience in supplier quality within the medical device industry. Familiarity with FDA regulations, ISO 13485, and auditing skills are crucial. Certifications like CQE or CQA are preferred.

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Can I expect to travel as a Supplier Quality Engineer at Frida?

Yes, as a Supplier Quality Engineer at Frida, you can expect to travel approximately 20-30% of the time. This travel is primarily for supplier audits and assessments, allowing you to engage directly with suppliers and ensure adherence to our quality standards.

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What kind of continuous improvement initiatives will I lead as a Supplier Quality Engineer at Frida?

In the role of Supplier Quality Engineer at Frida, you will be responsible for identifying and implementing continuous improvement initiatives that enhance supplier processes and product reliability. This may include working closely with suppliers to minimize defects and streamline their operations.

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What does cross-functional collaboration look like for the Supplier Quality Engineer at Frida?

At Frida, the Supplier Quality Engineer will collaborate extensively with Operations, Engineering, and Procurement teams to address any supplier-related manufacturing issues. You will also participate in Design Review meetings to share insights on supplier capabilities and constraints, fostering a team-oriented environment.

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Common Interview Questions for Supplier Quality Engineer
How do you approach supplier audits in a compliance-driven environment?

In a compliance-driven environment, I approach supplier audits by first preparing a detailed audit plan based on relevant regulations, such as FDA and ISO standards. During the audit, I carefully assess processes and documentation, engage with supplier personnel, and ensure that corrective actions are identified for any nonconformances.

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Can you explain your experience with risk management methodologies?

Absolutely! My experience with risk management methodologies involves applying tools like FMEA and FTA to identify potential failure modes and analyze their impacts. I prioritize risks based on their severity and occurrence, which informs my approach to developing mitigation strategies in collaboration with suppliers.

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What steps do you take to develop an Approved Supplier List?

To develop an Approved Supplier List, I begin by analyzing supplier performance through metrics such as compliance and defect rates. I conduct thorough risk assessments and capability evaluations, ensuring that only suppliers who meet our quality and regulatory standards are added to the list.

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How have you handled a major quality issue with a supplier in the past?

In handling a major quality issue with a supplier, I first conducted a detailed investigation to determine the root cause of the problem. I collaborated with the supplier to brainstorm corrective and preventive actions while maintaining open communication to ensure transparency and build trust.

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How do you stay updated on changes in FDA regulations and ISO standards?

I stay updated on changes in FDA regulations and ISO standards by regularly attending industry seminars, subscribing to relevant publications, and being a member of professional organizations. Networking with other quality professionals also enables me to share insights and best practices.

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What quality metrics do you find most important when assessing supplier performance?

I consider defect rates, compliance rates, and timely corrective action implementation to be critical quality metrics when assessing supplier performance. These metrics provide a comprehensive view of a supplier's ability to maintain standards and meet regulatory requirements.

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How do you foster strong relationships with suppliers?

To foster strong relationships with suppliers, I prioritize open communication and collaboration. I engage suppliers in discussions about quality expectations, conduct joint problem-solving sessions, and celebrate their achievements in meeting our standards to reinforce a partnership approach.

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Describe a situation where you successfully led a quality improvement initiative.

I led a successful quality improvement initiative by first gathering data on defect trends and identifying key areas for enhancement. I formed a cross-functional team that implemented process improvements, resulting in a 30% reduction in defects within six months, which significantly improved overall product quality.

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How do you ensure compliance with international standards in supplier management?

I ensure compliance with international standards by conducting thorough audits and keeping detailed records of supplier practices aligned with those standards. I also provide training and resources to suppliers to help them understand and implement the necessary requirements.

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What experience do you have with documentation control in quality systems?

I have extensive experience with documentation control in quality systems, which includes developing, reviewing, and maintaining standard operating procedures and quality records. I use various document management software systems to ensure all documentation is accessible and complies with regulatory requirements.

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Fridababy is the brand that gets parents. That means you. We are not a lifestyle. Far from it. We are a solution-based brand. The 411 of parenting. The who-do-I-call-in-the-middle-of-the-night-cause-my-baby-won&s;t-stop-screaming brand.

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Full-time, hybrid
DATE POSTED
March 19, 2025

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