Quality Assurance Specialist II

Posted 2 Days Ago
Be an Early Applicant
Carlsbad, CA, USA
In-Office
95K-110K Annually
Junior
Healthtech
The Role
Support and maintain the Quality Management System to ensure compliance with medical device regulations (ISO 13485, 21 CFR 820, MDSAP). Assist QMS procedure implementation, internal audits, CAPA facilitation, complaint handling, document review, QMS metrics and reporting, and cross-functional health hazard evaluations to support regulatory compliance and product introductions.
Summary Generated by Built In

The primary responsibility of the Quality Assurance Specialist II includes supporting ATEC’s quality system in compliance with ISO 13485, 21CFR820 and MDSAP. This position will ensure that auditing activities to maintain compliance, and support Document Control and Compliance Departments. This role supports the development and operation of the Quality Management System (QMS) at Alphatec Spine. This position also supports compliance to applicable domestic and international regulatory medical device regulations such as Part 820, 1271, MDD 93/42/EEC, ISO 13485:2003, Australian Therapeutic Goods (TGA), Japan (MHLW/PMDA).

Essential Duties and Responsibilities

  • Assist in the establish of systems to assure compliance with domestic (21CFR820) and international regulations (Australia: Australian Therapeutic Goods Administration, Japan: MHLW/PMDA
  • Assist in implementation of changes for QMS procedures and policies to ensure compliance to ISO 13485 and specific country requirements. Partners with appropriate stakeholders to define, recommend and implement QMS process improvements.
  • Plans and coordinates quality/compliance activities, identify roadblocks, and strategizes on various compliance paths for new products.
  • Review documents to ensure regulatory compliance
  • Designs, implements and maintains the quality systems ensuring compliance requirements
  • Supports internal QMS audits as needed for compliance.
  • Assists with Health Hazard Evaluations (HHE) with cross functional team members.
  • Facilitates CAPAs as needed to ensure compliance along with timeliness of completion.
  • Supports development of key QMS metrics. Provides analysis and reporting for Monthly Trend and Management Review Meetings.
  • Assist the complaint handling system in accordance with domestic and international regulatory requirements, as needed.
  • Performs other duties as assigned or required.

Requirements

The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Experience with quality system elements pertaining to medical devices and QMSR, QSR, cGMP and ISO 13485 and MDSAP familiarity is preferred.
  • Ability to work independently, but equally in a team environment
  • Strong written and very communication skills and attention to detail
  • Self-starting, detailed oriented, quick learner, creative and analytical
  • Capable of understanding and analyzing complex engineering problems
  • Demonstrated leadership, and ability to solve problems and communicate issues
  • Understanding of documentation system and management
  • Experience in an FDA regulated environment desirable
  • Microsoft Office knowledge, including Word and Excel, is a strong preference. Experience with SAP or Oracle Cloud system is a plus.
  • Ability to communicate effectively with all levels of the organization
  • Ability to prioritize multiple projects
  • Ability to resolve conflicting interests and obtain cooperation

Education and Experience

  • Typically requires a Bachelor’s Degree and minimum of 2 years medical device experience

For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable).

ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws.

Salary Range

Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate’s qualifications, education, skill set, years of experience, and internal equity. $95,000 to $110,000 Full-Time Annual Salary


Benefits
  • Health Care Plan (Medical, Dental & Vision)
  • Retirement Plan (401k, IRA)
  • Life Insurance (Basic, Voluntary & AD&D)
  • Paid Time Off (Vacation, Sick & Public Holidays)
  • Family Leave (Maternity, Paternity)
  • Short Term & Long Term Disability
  • Free Food & Snacks
  • Stock Option Plan

Skills Required

  • Bachelor's Degree
  • Minimum of 2 years medical device experience
  • Experience with quality system elements pertaining to medical devices (QMSR, QSR, cGMP, ISO 13485)
  • MDSAP familiarity
  • Experience in an FDA regulated environment
  • Microsoft Office knowledge, including Word and Excel
  • Experience with SAP or Oracle Cloud systems
  • Ability to work independently and in a team environment
  • Strong written and verbal communication skills and attention to detail
  • Self-starting, detail oriented, quick learner, creative and analytical
  • Capable of understanding and analyzing complex engineering problems
  • Demonstrated leadership and problem solving ability
  • Understanding of documentation systems and management
  • Ability to prioritize multiple projects and resolve conflicting interests
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Carlsbad, CA
818 Employees
Year Founded: 1990

What We Do

ATEC Spine is a medical device company dedicated to revolutionizing the approach to spine surgery through innovation. ATEC’s Organic Innovation Machine™ is the greatest concentration of spine know-how in the industry and committed to the creation of clinical distinction. Leveraging 100% spine focus and expertise, we seek to improve spine surgery by rethinking, redesigning and seamlessly integrating the technologies required from the ground up. The innovation that results from that process is being rapidly adopted because, like us, spine surgeons covet informatic and procedural sophistication that enables more predictable, more reproducible care. Our flagship technology, the Prone TransPsoas (PTP™) Procedure, leveraged decades of experience to advance first-generation lateral surgery with a more familiar patient position and elevated neuromonitoring.   EOS imaging, the backbone of ATEC’s informatic ecosystem, provides radiographic imaging, enabling standing, full-body, global alignment assessments. We are further developing EOS technology to elevate spine care with unprecedented capabilities. Our vision is to be the standard bearer in spine. Visit our website for more information: www.atecspine.com

Similar Jobs

In-Office
San Diego, CA, USA
114 Employees
60K-70K Annually
In-Office
San Diego, CA, USA
317 Employees
60K-70K Annually
In-Office
Torrance, CA, USA
64 Employees
25K-30K Hourly
In-Office
La Verne, CA, USA
14337 Employees
124K-160K Annually

Similar Companies Hiring

Sailor Health Thumbnail
Healthtech • Social Impact • Telehealth
New York City, NY
20 Employees
Granted Thumbnail
Artificial Intelligence • Healthtech • Insurance • Mobile • Financial Services
New York, New York
23 Employees
OneImaging Thumbnail
Healthtech
Miami, FL
62 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account