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Sonova
Senior Manager, Quality System
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Based on California data
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What they do
A Quality Assurance Manager focuses on prevention of mistakes and defects in manufacturing products. Develops procedures to ensure that quality standards are maintained. Manages all steps related to quality assurance as part of the quality management strategy of a company. May involve leadership of a team of quality assurance supervisors, specialists, and other associated staff members.
$118,988 / year median in California
-4% projected decline
Job Description
Senior Manager, Quality System Sonova - 3.2 Valencia, CA Job Details $131,156 a year 15 hours ago Benefits Paid parental leave Paid holidays Disability insurance Health insurance Dental insurance Flexible spending account Tuition reimbursement Paid time off Parental leave Employee assistance program Vision insurance 401(k) matching Opportunities for advancement Life insurance Qualifications Medical device manufacturing facility experience Regulatory/legal compliance standards in production Quality standards in production Biomedical regulatory compliance Stakeholder relationship building Stakeholder management Full Job Description Who we are At Sonova, we envision a world where everyone can enjoy the delight of hearing. This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection - from personal audio devices and wireless communication systems to hearing aids and cochlear implants. We're dedicated to providing outstanding customer experiences through our global audiological care services, ensuring that everyone has the opportunity to engage fully with the world around them. Guided by a culture of continuous improvement that fosters resilience and self-motivation, our team is united by a shared commitment to excellence and a deep sense of pride in our work, each of us playing a vital role in creating meaningful change, Here you'll find a diverse range of opportunities that span both consumer and medical solutions and the freedom to shape your career while making an impact on the lives of others. Join us in our mission to create a more connected world, where every voice is heard and every story matters. Valencia (CA), United States Senior Manager, Quality System 164552 Valencia, CA Senior Manager, Quality Systems Advanced Bionics is seeking a Senior Manager, Quality Systems to lead core global quality system functions within the Quality Assurance organization. This role is responsible for ensuring quality system processes operate effectively, compliantly, and in alignment with business needs across Advanced Bionics sites. This leader will oversee key quality system areas including audit management, CAPA, training management, document control, records, and computerized quality system software validation while driving continuous improvement and regulatory compliance.
Responsibilities:
Lead core global quality system functions, including internal and external audit management, distributor audit management, CAPA, training management, document control, records, and computerized quality system software validation Develop, maintain, and continuously improve global quality system processes and procedures to meet regulatory and business requirements Establish quality system goals, metrics, and operating mechanisms to assess and improve effectiveness across Advanced Bionics sites Provide leadership reporting on quality system performance, compliance status, risks, trends, and improvement opportunities Manage the internal audit program and support external audits and inspections by regulatory agencies and notified bodies Oversee distributor audit processes in alignment with regulatory requirements, quality agreements, and risk-based principles Coach, develop, and manage team members through performance management, development planning, hiring, and resource planning More about you: BA/BS degree required, or demonstrated equivalent experience; graduate degree in science or business preferred 6+ years of experience in a GMP, QSR, and ISO-regulated medical device environment 5+ years of progressive management experience and experience working in a cross-functional matrix environment 3+ years of Class III medical device experience within a Quality function Strong knowledge of quality system regulations, includingISO 13485, MDSAP, EU MDR, 21 CFR
820, and Part 11 Proven experience developing, improving, and maintaining quality system documentation and processes Strong leadership, communication, analytical, problem-solving, and stakeholder management skills A minimum of 200Mb/sec download and 10Mb/sec upload speed internet connectivity is required to support any remote/hybrid employee functionality at Sonova Don't meet all the criteria? If you're willing to go all in and learn we'd love to hear from you! We are looking forward to receiving your application via our online job application platform. For this position only direct applications will be considered. Sonova does not recruit via app, telegram, carrier pigeon or any other format that does not include speaking with an actual human. If you are offered a job without speaking with someone please contact Sonova Human Resources What we offer : Medical, dental and vision coverage- Health Savings, Health Reimbursement, Flexible Spending/Dependent Care Accounts TeleHealth options 401k plan with company match
- Company paid life/ad&d insurance Additional supplemental life/ad&d coverage available Company paid Short/Long-Term Disability coverage (STD/LTD) STD LTD Buy-ups available Accident/Hospital Indemnity coverage Legal/ID Theft Assistance PTO (or sick and vacation time), floating Diversity Day, & paid holidays
- Paid parental bonding leave Employee Assistance Program (24/7 mental health support hotline, 5 company paid counseling sessions and more) Robust Internal Career Growth opportunities Tuition reimbursement Hearing aid discount for employees and family Internal social recognition platform Plan rules/offerings dependent upon group Company/location.