ZipRecruiter

Log In

1

Support Quality Associate Jobs (NOW HIRING)

Podimetrics

Quality Associate

Somerville, MA · On-site

Job Title: Quality Associate Department: Quality and Regulatory Location: On-site at HQ in ... Support Quality Engineering with post-market surveillance activities, including trending device ...

IDEXX

Quality Associate

Westbrook, ME · On-site

$20 - $22/hr

You will maintain accurate documentation, complete data entry, and support quality systems that ... Associate degree or equivalent preferred * Ability to read, interpret and carry out detailed ...

Hawkins

Quality Associate - Pharm

Minneapolis, MN · On-site

$24 - $25/hr

A Quality Associate is expected to implement processes and procedures to sustain and improve the ... Safety * Takes personal accountability and leadership to support and continuously foster a ...

Maxonic

Quality Associate I

Franksville, WI

$24/hr

In support of their needs, we are looking for a Quality Associate I. Job Title: Quality Associate I Job Type: Contract Job Location: Franksville, WI Work Schedule: Onsite Pay Rate: $24, Based on ...

Careers | CET

Quality Associate

Bristol, RI

Summary The Quality Associate supports both quality assurance and quality control initiatives regarding Production and Operations to ensure that customer requirements are met, and any discrepancies ...

H & T Nevada LLC

Quality Associate

Sparks, NV · On-site

Description POSITION SUMMARY The Quality Associate is responsible for ensuring outgoing parts meet ... This role supports production by performing inspections, documenting results, identifying defects ...

H&T Recharge

Quality Associate

Sparks, NV · On-site

Job Type Full-time Description POSITION SUMMARY The Quality Associate is responsible for ensuring ... This role supports production by performing inspections, documenting results, identifying defects ...

Conexus Food Solutions

Quality Associate

Chicago, IL · On-site

$23 - $26/hr

What You'll Do As a Quality and Inventory Control Associate, your primary role is to ensure that ... Supporting ERP/PDA scanner testing and ensuring accurate inventory data entry across systems.

PEI GENESIS INC.

Quality Associate

South Bend, IN · On-site

$15.94 - $18/hr

Our Quality Department has an opening for a Quality Associate that works Monday - Friday, 9:00 AM ... This position supports the continuous flow of quality test cell activities by testing and ...

PEI GENESIS INC.

Quality Associate

South Bend, IN · On-site

$15.94 - $18/hr

Our Quality Department has an opening for a Quality Associate that works Monday - Friday, 9:00 AM ... This position supports the continuous flow of quality test cell activities by testing and ...

Bora Pharmaceuticals

Quality Associate

Maple Grove, MN · On-site

$52K - $67K/yr

The Quality Associate issues cGMP documentation to operations in support of manufacturing and packaging operations. Reviews executed manufacturing/packaging documentation and dispositions batch ...

Conexus Food Solutions

Quality Associate

Chicago, IL · On-site

What You'll Do As a Quality and Inventory Control Associate, your primary role is to ensure that ... Supporting ERP/PDA scanner testing and ensuring accurate inventory data entry across systems.

next page

Showing results 1-20

All JobsBusiness JobsCustomer Service JobsCustomer Service Representative JobsSupport Quality Associate Jobs

Support Quality Associate information

See salary details

$10

$19

$28

How much do support quality associate jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for support quality associate in the United States is $19.57, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $21.15 per hour, depending on experience, location, and employer.

What cities are hiring for Support Quality Associate jobs?

Cities with the most Support Quality Associate job openings:

What states have the most Support Quality Associate jobs?

States with the most job openings for Support Quality Associate jobs include:

What are popular job titles related to Support Quality Associate jobs?

For Support Quality Associate jobs, the most frequently searched job titles are:

Quality Associate

Somerville, MA • On-site

Podimetrics
11 - 50 employees
Learn more about Podimetricsexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 26 days ago

Job description

Job Title: Quality Associate
Department: Quality and Regulatory
Location: On-site at HQ in Somerville, MA
Reports to: Director, Quality and Regulatory
Key Relationships: Sr. Quality Engineer, Device Operations, Sustaining Engineering, Clinical Support
About Podimetrics:
Founded in 2011, Podimetrics set out on a mission to improve patient lives through early detection and prevention of diabetic foot ulcers, the leading cause of lower limb amputations. Podimetrics has since evolved to become a rapidly growing virtual care management company with advanced technology and patient-centered services.
Today, Podimetrics teams with and provides solutions to patients, payers and providers that alleviate the health and financial implications of diabetic foot complications in high-risk populations. We are a mission driven, financially responsible enterprise that enables patients to stand on their own feet and live more independent and fulfilling lives.
Core Values:
  1. Mission First: We are here to drive critical change, bring hope and compassionate care to those in great need.
  2. People Matter Most: We advance our mission by caring for our people (colleagues, patients, providers, customers and stockholders), treating them with kindness and respect.
  3. Courageous Action: We are driven to act and demand mutual accountability. We believe that missteps foster learning and iterative improvement.
  4. Healthy Debate: We commit to transparent discussion and resulting decisions. The very best decisions come from differing points of view, requiring good intentions, mutual trust and no ego.
  5. Deep Curiosity: We are always striving to learn more and do better. We question if the best we have ever done couldn't be improved further.

Role Description:
We are seeking a highly driven, organized, and detail-oriented Quality Associate to support a broad set of responsibilities across the Quality and Regulatory Affairs department. This role sits at the center of post-market surveillance, complaint handling, document control, and audit/CAPA support, and requires fluid movement between hands-on patient device data, formal quality system documentation, and cross-functional collaboration. The Quality Associate will work closely with Regulatory Affairs, Quality Engineering, Device Operations, Sustaining Engineering, and Clinical Support Services on a day-to-day basis. The ideal candidate is analytical, highly organized, and energized by building structure into a growing quality system - triaging patient feedback into formal complaints, keeping the document control environment current and audit-ready, supporting proactive post-market surveillance through data trending and remote device monitoring, and assisting with internal audits and corrective actions.
Key Responsibilities:
Complaint Handling & Post-Market Surveillance
  • Review incoming patient feedback on a daily basis and determine whether it meets the criteria for a formal complaint per FDA and ISO 13485 requirements.
  • Initiate the complaint process within the quality system for qualifying feedback, including opening complaint records and conducting initial investigations.
  • Support Quality Engineering with post-market surveillance activities, including trending device issue data and maintaining visibility into recurring or emerging performance issues.
  • Conduct remote monitoring of devices in the field to proactively identify potential issues and initiate timely device replacements, ensuring patients experience uninterrupted use of Podimetrics devices.
  • Coordinate with Device Operations, Sustaining Engineering, and Clinical Support Services to resolve complaints and drive improvements to device performance and customer experience.

Document Control
  • Own day-to-day document control responsibilities across multiple document tiers within the quality management system (e.g., procedures, work instructions, and forms/records).
  • Support document review, revision, routing, approval, and archival processes, ensuring documents remain current, accurate, and audit-ready.
  • Maintain document control records in accordance with change control procedures and quality system requirements.

Audits & Corrective Actions
  • Assist with the internal audit program, including conducting monthly audits within the quality system.
  • Provide support for corrective and preventive actions (CAPA), including documentation, tracking, and follow-up on action items.
  • Support preparation and coordination for external and regulatory audits or inspections as needed.

Quality Management System (QMS) Administration
  • Assist in maintaining the QMS software platform, with a focus on training management and document control functionality.
  • Manage day-to-day quality operations and maintain QMS workflows, incorporating observations and data trends as they arise.

Qualifications:
  • Bachelor's degree required; Master's degree in Regulatory Affairs, Quality Systems, or a related field preferred.
  • Minimum of 2 years of experience in the medical device industry, with familiarity with FDA 21 CFR 820 and ISO 13485 requirements.
  • Experience with complaint handling, document control, or QMS software (eQMS) strongly preferred.
  • Experience supporting internal audits or CAPA processes is a plus.
  • Demonstrated ability of analytical thinking and problem-solving skills.
  • Proficient in the use of Microsoft Office suite.
  • Experience working in a fast-paced environment.
  • Excellent organizational skills and high attention to detail, particularly in documentation review.
  • Excellent English written and verbal communication.
  • Strong collaboration skills and team orientation.

Critical Competencies:
Critical Thinking: Demonstrates analytic and problem-solving skills and understands the impact of individual decisions on other parts of the organization.
Attention to Detail: High attention to detail and a meticulous, organized approach to documentation review and document control.
Communication Skills: Excellent written and verbal communication skills. Ability to present data and articulate ideas in front of an audience.
Resourcefulness: Finds creative solutions to difficult problems, doing a lot with a little.
Teamwork: Respects colleagues and works well within and across teams. Motivates team members to achieve high performance through collaboration and fellowship.
Adaptability: Embraces and adjusts quickly to change. Ability to work and thrive in a fast-paced environment.
Benefits:
  • Base Pay: $65k - $85k base salary commensurate with experience
  • Individual Bonus Opportunity
  • Equity Options
  • Flexible Paid Time Off (Guaranteed four (4) weeks of PTO)
  • Paid Sick Leave (up to forty (40) hours annually)
  • Fully Paid Parental Leave (twelve (12) weeks for birthing parents, eight (8) weeks for non-birthing/adoptive parents)
  • Competitive Medical, Dental, and Vision plans - Podimetrics covers 80% of premiums.
  • Health Savings Account with employer contribution
  • Employee Assistance Program - Free, confidential advice for team members who need help with stress, anxiety, financial planning, and legal issues.
  • 401k
  • Life Insurance - Podimetrics pays 100% of the cost of Basic Life & Personal Accident
  • Disability insurance - Podimetrics pays 100% of the cost of Short-Term and Long-Term Disability Insurance
  • Additional life insurance, critical illness, and accident coverage are available

Podimetrics is committed to a diverse and inclusive workplace. We are an equal opportunity employer and do not discriminate based on race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status.

Apply