What are the responsibilities and job description for the Senior Director, Quality position at QAPEL MEDICAL INC?
Position Title : Senior Director, Quality Job Location : Fremont, HQ
Department : Quality Worker Category : Full-Time / Exempt
Industry : Neurovascular / Medical Devices
About Q’Apel :
At Q’Apel, we are passionate about revolutionizing neurovascular access. In the simplest sense, we’re a company that creates solutions. We design novel access device technology for vascular interventions and unmet clinical needs. Successful Q’Apel team members step up to the plate and work together to achieve our goals every single day. We are a fast-paced, high-growth company with a startup philosophy which requires an all-hands-on-deck attitude, taking on all changes with excitement and a great attitude.
Who We Want :
As a pivotal member of the leadership team, the Senior Director of Quality will be responsible for the day-to-day management of quality operations including assuring all areas operate in support of the company and department objectives and in compliance with applicable regulations and standards. This role includes the oversight of incoming inspection, manufacturing QC, sterilization, product acceptance testing and release, document control, equipment management, supplier management, manufacturing process verifications / validations, as well as associated nonconformance control, equipment impact assessments, supplier corrective actions, and CAPAs.
What You’ll Work On :
- Facilitate, maintain, and implement Best in Class Quality Management improvements to quality operations while maintaining compliance with applicable Quality System Regulations, Medical Device Regulations, and ISO standards (including, but not limited to 13485, 14971, 11135, and EU MDR) and in consideration to the needs of a small to mid-size business.
- Take a leadership role in achieving strategic quality initiatives including the establishment of project aspects such as scope, schedule, resources, risks, deliverables / milestones according to released Quality Plans, and leadership to drive towards meeting the objectives.
- Provide leadership, direction, and mentorship to quality personnel; including but not limited to inspectors, engineers, specialists, consultants, and cross-functional areas as needed to ensure compliance with applicable federal and state regulations, international standards, and the company’s Quality Policy.
- Assure timely lot release of commercial products including sterilization processing, biological testing, quality inspections, and testing, and review of lot history records.
- Responsible for the collection, analysis, and actions taken for Quality / business metrics and metrics to be provided and reviewed with cross-functional management through quality reports and management reviews.
- Support, participate, and defend operational quality management system areas during audits as the subject expert.
- Meet completion dates for assigned projects, internal and external audit observations related to operations quality, CAPA plans, procedural updates, and other duties as assigned.
- Work interactively with cross-functional teams within a small / medium company environment to facilitate results and accomplishments.
- Continually identify and implement improvements and changes to current operational processes using scalable quality tools and solutions to meet Q’Apel’s current and future needs. Improvements may be identified through observation of daily operations, gap analysis, audits, and departmental reviews.
- Ensure operational quality assurance goals are aligned with department and company objectives. Develop or provide input to SMART goals, development plans, performance evaluations, and other personnel reviews for subordinates as required.
- Leader and influencer of others by motivating, training, and inspiring personnel to achieve high-quality products and a culture that supports Q’Apel’s Quality Policy and compliance with our Quality Management System.
- Participate in industry and other professional networks to ensure awareness of industry standards, trends, state-of-the-art, and best practices in order to strengthen Quality System knowledge.
- Other duties as assigned.
What You Bring : Education :
Experience & Skills :
Our salary ranges are calculated by role and level. Your position within that range will be determined by your job-related knowledge, skills, experience, relevant education, and training / certifications. In addition to those factors, we also examine internal equity as well as consider the current market rate, and the title may be assessed one level lower or higher accordingly. After you join the company your performance, contributions, and results along with business and organizational needs will affect your base salary. The base salary range for this full-time position is between $220,000 to $260,000 equity benefits.
This document contains confidential, proprietary information of Q’Apel Medical, Inc. It may not be copied or reproduced without prior written permission from Q’Apel Medical, Inc.
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Salary : $220,000 - $260,000