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Sr. Quality Specialist

Edgewell Personal Care · Coppell, TX

Apply on Edgewell ↗
Level
Senior
Team
Quality
Base pay
$84k–$126k
Degree
Preferred
Experience asked
5+ years
Industry
Industrial
Posted
10 days ago

The role in 30 seconds

A senior quality role at Edgewell Personal Care (industrial) in Coppell, TX. Review, develop, revise, and maintain quality procedures, specifications, work instructions, and quality records.

They ask for
5+ years · degree preferred
Tools it names
Root cause, CAPA, FDA / GMP, Supplier quality
Base pay
$84k–$126k

Read from the posting. The full description is below.

From the plant jobs report · week of November 2, 2026

Quality Engineer roles in Texas: typical posted base $90k–$126k. This one lists $84k–$126k.

Median of the low and high ends of 25 live postings that list pay, out of 90 quality engineer openings in Texas, read from manufacturers' own careers sites.

Texas plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 89 other live quality postings in Texas.

Base pay
In line with similar roles

Typical $90k–$121k, from 23 postings that list pay.

Experience asked
More than usual (5+ vs 3+)

Similar roles usually ask 3+ years.

Skills these teams ask for most

  • ✓ Root cause 67%
  • Lean 38%
  • Validation (IQ/OQ/PQ) 36%
  • ✓ New product launch 34%
  • FMEA 34%
  • ✓ Supplier quality 30%

✓ = this posting asks for it too. % = share of similar postings that mention it.

It asks for 5+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

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. 1

    Pick 2–3 people on the Quality team at Edgewell Personal Care

    Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.

  2. 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. 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 did you land the job? What stood out in your interviews?
  4. 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. 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.

This plant: Edgewell Personal Care in Coppell

1 other open role at this site.

Full description from Edgewell Personal CareAs posted on their careers site.Show

Position Summary

The Senior Quality Specialist is responsible for leading and coordinating key Quality System activities in support of contract manufacturing organizations, contract packaging organizations, suppliers, and distribution partners. The role serves as a technical resource within the Quality organization and is responsible for ensuring compliance with internal quality standards and applicable regulatory requirements.

The Senior Quality Specialist independently manages complex quality system activities, leads investigations and continuous improvement initiatives, drives issue resolution with internal and external partners, and provides guidance to other team members. The position plays a critical role in maintaining inspection readiness, supporting business continuity, and fostering a culture of quality excellence.

Experience/Education Required

  • ✓Minimum B.S. or B.A. – Science or Engineering Degree preferred
  • ✓Minimum 5 years of experience in Quality Assurance, Quality Systems, Supplier Quality, Manufacturing Quality, or a related discipline.
  • ✓Knowledge of regulated products and quality systems. (Health Canada, FDA, etc.)
  • ✓Experience with investigations, CAPA, change control, and document management processes.
  • ✓Strong organizational, analytical, and problem-solving skills.

Skills and Abilities Required

  • ✓Strong verbal / written communication, interpersonal, and influencing skills. Ability to interface with internal and external customers at all levels. Ability to clearly communicate technical and non-technical information verbally and in writing.
  • ✓Excellent organizational, prioritization skills and problem-solving skills to successfully handle multiple priorities and projects simultaneously.
  • ✓Ability to think and act independently and make sound decisions.
  • ✓The position may also require travel to other company locations and to external meetings, suppliers, etc.
Show full description ↓

Edgewell is a global team of over 6,000 visionaries, doers and makers. Our secret is people, and we have an inspiring and collaborative global force of them. Our portfolio of over 25 brands touches lives in more than 50 countries by making useful things joyful. Together, we reimagine good mornings and endless summers, strive for more sustainable ways to beautify and bond, and do it all with not only confidence but determination.

Quality Systems Management

  • •Lead daily execution and continuous improvement of assigned Quality System processes.
  • •Ensure quality records are maintained in compliance with company procedures and regulatory requirements.
  • •Support inspection readiness activities and preparation for internal, customer, and regulatory audits.
  • •Identify opportunities to improve quality system effectiveness and efficiency.

Investigation, CAPA & Risk Management

  • •Independently lead investigations related to deviations, nonconformances, complaints, and quality events.
  • •Facilitate root cause analysis and development of effective corrective and preventive actions.
  • •Monitor CAPA effectiveness and identify recurring trends requiring escalation or systemic improvement.
  • •Conduct risk assessments and provide recommendations using science and risk-based decision-making principles.

External Partner Quality Oversight

  • •Support quality oversight of suppliers, contract manufacturers, co-packers, and distribution partners.
  • •Participate in supplier performance monitoring and quality reviews.
  • •Collaborate with external partners to resolve quality concerns and implement improvements.
  • •Support supplier qualification, change management, and ongoing performance evaluations.
  • •Support new product introductions, product transfers, process changes, and supplier changes.

Audit & Compliance Support

  • •Participate in internal, supplier, and third-party audits.
  • •Assist in audit preparation, response development, and corrective action implementation.
  • •Track audit findings and support timely closure of commitments.
  • •Ensure compliance with applicable FDA, Health Canada, GMP, and company quality requirements.

Documentation & Data Management

  • •Review, develop, revise, and maintain quality procedures, specifications, work instructions, and quality records.
  • •Ensure documentation is accurate, complete, and maintained within approved systems.
  • •Analyze quality metrics and trend data to identify improvement opportunities.
  • •Prepare reports, presentations, and quality summaries for management review.

Continuous Improvement & Project Leadership

  • •Lead quality improvement initiatives focused on compliance, efficiency, and risk reduction.
  • •Support product launches, product transfers, supplier changes, and business initiatives.
  • •Participate on cross-functional project teams as the Quality representative.
  • •Recommend and implement process improvements across the External Quality network.

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