Overview
On Site
Competitive
Contract - W2
Contract - Contract
No Travel Required
Skills
Root Cause Analysis
Corrective and Preventive Actions (CAPA)
Computer System Validation (CSV)
FDA Compliance cGMP (Current Good Manufacturing Practices)
Internal Auditing
Quality Management Systems (QMS)
Equipment & Process Validation
Cleaning Validation
Annual Product Review (APR)
Stability Testing / Stability Programs
OTC Manufacturing
Documentation
Control
Change Control Risk Assessment
Regulatory Compliance
Quality Investigations
Batch Record Review
Validation Protocols
Inspection Readiness
Quality Assurance (QA)
Certified Quality Auditor (CQA)
Certified Quality Engineer (CQE)
Job Details
Are you a Quality Engineer with a passion for ensuring product integrity and regulatory compliance in a manufacturing environment? We re looking for a hands-on quality professional to lead root cause investigations, support validation efforts, and drive continuous improvement across our quality systems all within a highly regulated GMP setting.
Must be local to the Dallas-Fort Worth area onsite required
W2 only no C2C or third-party submissions accepted
This is not a software QA position this role supports manufactured products (e.g., cosmetics, OTC, pharma, or nutraceuticals) and requires direct experience with FDA, GMP, and physical product quality systems.
What You ll Be Doing:
If you re ready to apply your quality expertise where it matters most in the physical products people rely on every day we d love to connect.
#QualityEngineer #ManufacturingQA #GMPJobs #FDACompliance #CSV #RootCauseAnalysis #ValidationJobs #OTCManufacturing #StabilityTesting #DFWJobs
Estimated Min Rate: $30.00
Estimated Max Rate: $42.00
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit ;to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship, potentially resulting in the withdrawal of a conditional offer of employment.
Must be local to the Dallas-Fort Worth area onsite required
W2 only no C2C or third-party submissions accepted
This is not a software QA position this role supports manufactured products (e.g., cosmetics, OTC, pharma, or nutraceuticals) and requires direct experience with FDA, GMP, and physical product quality systems.
What You ll Be Doing:
- Lead product quality investigations and root cause analyses (CAPA)
- Support cleaning, equipment, and process validation initiatives
- Oversee computer system validation (CSV) efforts for manufacturing systems
- Contribute to Annual Product Reviews and stability program activities
- Perform internal audits and support FDA or regulatory inspections
- Collaborate with manufacturing, R&D, packaging, and quality teams
- Bachelor s degree in Chemistry, Microbiology, or a related field
- 3+ years of QA/QC experience in regulated product manufacturing
- Hands-on experience with CSV, CAPA, and GMP documentation
- Knowledge of stability programs and validation processes
- Familiarity with OTC, pharma, cosmetics, or similar industries
- CQE, CQA, or similar certifications a plus
If you re ready to apply your quality expertise where it matters most in the physical products people rely on every day we d love to connect.
#QualityEngineer #ManufacturingQA #GMPJobs #FDACompliance #CSV #RootCauseAnalysis #ValidationJobs #OTCManufacturing #StabilityTesting #DFWJobs
Estimated Min Rate: $30.00
Estimated Max Rate: $42.00
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit ;to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship, potentially resulting in the withdrawal of a conditional offer of employment.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.