
Senior Quality Control Technician
Enovis · California
- Level
- Technician
- Team
- Quality
- Degree
- Required (or equivalent experience)
- Industry
- Medical devices
- Posted
- 23 days ago
The role in 30 seconds
An engineer-level quality role at Enovis (medical devices) in California. Update, revise, and maintain controlled procedures, work instructions, and quality documents.
- They ask for
- degree required (or equivalent experience)
- Tools it names
- Root cause, ISO 9001, AS9100, ISO 13485, Internal audits
- Day to day
- some off-shift / weekend coverage
Read from the posting. The full description is below.
How this role compares
Against 32 other live quality postings in California.
- Experience asked
- Not stated
Similar roles usually ask 4+ years.
Skills these teams ask for most
- Team leadership 55%
- ✓ Root cause 36%
✓ = this posting asks for it too. % = share of similar postings that mention it.
Stands out: this posting asks for ISO 13485, which few similar roles mention. If you have it, lead with it.
At a glance
Pulled from the posting text. If it's not listed here, the posting didn't say.
How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Quality team at Enovis
Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.
- 2
Send a short, curious note
One real question about their work. No favors yet. Each person gets a different note, written for this role.
- 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
- How much of the job is customer complaints versus prevention?
- How does off-shift and weekend coverage work?
- How did you land the job? What stood out in your interviews?
- 4
Apply with someone vouching for you
If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.
- 5
Bring proof to the interview
One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.
Full description from EnovisAs posted on their careers site.ShowHide
What You'll Do
At Enovis™ we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence — with the goal of transforming medical technology as we know it.
Because that’s how we change the lives of patients for the better. And that’s how we create better together.
Key Responsibilities
- ◆Administer and maintain the site training program, ensuring employee training records are current and compliant with QMS requirements.
- ◆Coordinate training assignments, track completion, and support training effectiveness evaluations.
- ◆Partner with department leads to ensure training needs are identified and addressed.
- ◆Update, revise, and maintain controlled procedures, work instructions, and quality documents.
- ◆Support QMS improvements by identifying gaps and contributing to corrective and preventive actions .
- ◆Prepare documentation, records, and evidence for internal audits, customer audits, and regulatory inspections.
- ◆Participate in audit activities and support follow‑up actions to ensure compliance and readiness.
- ◆Oversee QC teams across incoming inspection, in ‑ process inspection, and final product release.
- ◆Assist with inspection planning, sampling, and verification of inspection results.
- ◆Conduct stock checks and inventory verification to ensure product status accuracy.
- ◆Work closely with Quality Engineers to support investigations, root cause analysis, and quality improvement initiatives.
- ◆Coordinate nonconforming material activities, including identification, segregation, documentation, and disposition routing. Ensure timely review and closure of NCMRs, support root‑cause investigations, and collaborate with Quality Engineers, Supply Chain, and Operations to prevent recurrence.
Currently, Enovis does not provide sponsorship for employment visas (e.g., H-1B) and will not offer such sponsorship in the future. Applicants must already have full-time work authorization in the United States, both now and in the future, without requiring sponsorship.
Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. 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 essential functions.
- ✓High school diploma or equivalent required; an associate degree or relevant certification preferred.
- ✓3 + years of experience in Quality Assurance or Quality Control within manufacturing or other regulated environments.
- ✓Working knowledge of QMS standards (ISO 9001, ISO 13485, AS9100).
- ✓Ability to read and interpret technical drawings, specifications, and inspection data.
- ✓Proficiency with inspection tools, techniques, and basic non ‑ destructive examination methods.
- ✓Experience in using ERP systems (e.g., Oracle) for transactions and reporting.
- ✓Strong communication , documentation, and organizational skills .
- ✓Demonstrated ability to lead or guide quality inspectors and support adherence to SOPs and standard work.
- ✓Effective interpersonal skills, including conflict resolution, collaboration, and active listening.
- ✓Ability to train others and support team development.
- ✓Self ‑ starter capable of working independently and maintaining confidentiality.
- ✓Proficient with computers and general office software.
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About enovis™
Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company’s extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit www.enovis.com .
Job Title
Senior Quality Control Technician
Reports To
Manager, Quality Assurance
Location
VMC (Vista Manufacturing Center)
Business Unit Description
Bracing and Supports
Role Summary
The Senior Quality Control Technician is an individual contributor who performs key Quality Management System (QMS) activities across the site, including training program administration, procedure updates, supplier nonconformance communication, and audit support. The role also provides functional oversight, guidance, and support for Quality Control (QC) activities, including incoming inspection, in-process checks, final release, and stock verification, without direct people-management responsibility. This position works closely with Quality Engineers, Operations, and Supply Chain to ensure compliance, product quality, and continuous improvement.
Work environment | Physical demands
Ability to sit and stand for long periods of time.
Ability to lift and carry 25 pounds.
“Creating better together ”. It’s the Enovis purpose, and it’s what drives us and empowers us every day on a global scale. We know that the power to create better – for our customers, our team members, and our shareholders – begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.
Watch this short on creating the next generation of better together at Enovis:
Better is... | Enovis
We offer a comprehensive benefits package which includes
- •Medical Insurance
- •Dental Insurance
- •Vision Insurance
- •Spending and Savings Accounts
- •401(k) Plan
- •Vacation, Sick Leave, and Holidays
- •Income Protection Plans
- •Discounted Insurance Rates
- •Legal Services
