drjobs Director, Design Quality Assurance - Pleasanton, CA

Director, Design Quality Assurance - Pleasanton, CA

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Pleasanton, CA - USA

Monthly Salary drjobs

$ 200000 - 230000

Vacancy

1 Vacancy

Job Description

Calyxo Inc. is a medical device company headquartered in Pleasanton California USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.

Are you ready to change the future of kidney stone treatment We are seeking high achievers who want to be part of a dynamic team working in a fun diverse atmosphere.

Summary:

The Director Design Quality Assurance provides strategic representation planning management direction and guidance to meet quality engineering goals and objectives supporting new product development and sustaining commercial products. This position directs and oversees Quality Engineering staff who contribute to and support new product development and sustaining of commercial products. The role provides leadership in defining and implementing quality engineering policies principles and processes that facilitate the realization of Calyxos product development objectives.

As an integral member of Calyxos Quality Leadership Team this position fosters greater teamwork alignment collaboration accountability and performance between Quality and R&D.

This position requires experience creating developing implementing managing overseeing and improving systems and processes and the ability to drive performance and service at the highest level in a fast-paced high growth dynamic medical device environment.

In This Role You Will:

  • Lead the Design Quality Assurance team and ensure compliance with applicable domestic and international regulatory standards (e.g. FDA CE marking etc.).
  • Oversee Design Quality Assurance and Engineering activities including the development documentation implementation and maintenance of quality system requirements and procedures related to design development and pre-production manufacturing activities.
  • Partner with R&D to ensure product development activities and deliverables are compliant with internal procedures external standards and regulations and industry best practices.
  • Provide Quality Engineering leadership resources and support to ensure the on-time development and commercialization of quality products.
  • Oversee and direct Quality staff to ensure ample coverage and support for the R&D team to support new product development (NPD)and sustaining product engineering.
  • Responsible for overseeing planning leading and driving activities such as Risk Management Biocompatibility Shelf-Life Studies Test Method Validation Reliability Engineering and Statistical Analysis in support of new product development product changes and sustaining product engineering.
  • Ensure robust design control software development and risk management practices are followed driving improvements in test methods validation and verification processes.
  • Champion quality engineering principles and foster a company-wide continuous improvement mindset promoting shared responsibility for quality.
  • Responsible for talent management including recruiting engaging training and developing quality staff to ensure the necessary skill sets and competencies to meet business needs.
  • Establish foster and maintain successful cross-functional relations with internal departments/functions such as Operations/Manufacturing R&D/Engineering Regulatory and Clinical Affairs.
  • Interface with all departments to provide leadership on the use of Quality Assurance and Engineering methodologies tools and regulatory compliance requirements
  • Serve as Subject Matter Expert for areas of responsibility during internal and external audits
  • Work in accordance with the quality system procedures related to work activities.
  • Develop establish monitor and report on functional quality objectives metrics and goals.
  • Manage department expenses in-line with approved department budgets.
  • Supporting department specific initiatives and projects as assigned.
  • Contribute to our culture of being collaborative respectful transparent ethical efficient high-achieving and fun!

Who You Will Report To:

  • See Organization Chart

Requirements:

  • Education: Bachelor of Science in Engineering or Life Science discipline.
  • Minimum 15 years experience in Quality Engineering/Assurance in the medical device industry including 5 years in a managerial role.
  • Work location: Pleasanton CA.
  • Travel: Ability to travel 10 - 15% Domestic and International to suppliers and contract manufacturing sites.
  • Full-time employment.
  • Strong knowledge of FDA requirements for design control of medical devices and 21 CFR 820; ISO 13485 and; IEC 60601-1 IEC 62304 and related regulations.
  • In depth knowledge of Risk Management Biocompatibility and Sterilization.
  • Strong written oral interpersonal skills analytical skills problem-solving techniques and statistical application experience.
  • Proactive leader who can determine deficiencies communicate them effectively through the organization and follow through to resolution.
  • Excellent level of organizational skills and ability to direct and oversee multiple projects/initiatives at the same time with a high level of attention to detail.
  • Strategic yet hands-on when needed; high degree of energy and drive; and the ability to continually seek to make improvements to the function process and people being led.
  • Excellent leadership and managerial skills with the ability to be flexible adaptable and to work under pressure.
  • Experience with FDA Class II sterile devices.
  • Compliance with relevant county state and Federal rules regarding vaccinations.

What We Offer:

At Calyxo you will be part of a knowledgeable high-achieving experienced and fun team. You will work in a diverse work environment with experienced proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself.

We also offer an attractive compensation package which includes:

  • A competitive base salary of $200000 - $230000 and variable incentive plan
  • Stock options ownership and a stake in growing a mission-driven company
  • Employee benefits package that includes 401(k) healthcare insurance and paid vacation

Calyxo is deeply committed to fostering an environment where diversity and inclusion are not onlyvalued but alsoprioritized. We believe a diverse and inclusive community empowers us to act courageously care deeply and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities which strengthen our focus and fuel our growth.

Calyxo is proud to be an equal opportunity employer seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race color religion gender gender identity or expression sexual orientation national origin genetics disability age veteran status or any other applicable legally protected characteristics

Legal authorization to work in the United States is required. In compliance with federal law all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

Disclaimer:

At Calyxo we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following:

  • Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture.
  • Verification of Identity: We do not extend job offers without first meeting candidates either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment.
  • Beware of Scams: Calyxo will never request sensitive personal information such as your full name address phone number or identification documents via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of. If you receive a request for information from any other domain please contact us directly at to verify the legitimacy of the communication.

We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.


Required Experience:

Director

Employment Type

Full Time

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.