FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
QA Engineer
Corden Pharma - A Full-Service CDMOQA Engineer leading GMP quality systems, equipment qualification, and validation for CordenPharma’s pharmaceutical manufacturing operations. Preparing protocols, reports, risk assessments, and Annual Product Reviews.
Posted 8/22/2026full-timeBoulder • Colorado • 🇺🇸 United StatesMid-LevelSenior💰 $90,000 - $108,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Quality Assurance processes, including equipment qualification, validation, and compliance with Good Manufacturing Practices. Proficient in generating and reviewing critical documentation while providing leadership and guidance in quality-related projects.
Highest-signal resume keywords
Quality Assurance LeadershipEquipment QualificationGood Manufacturing PracticesPharmaceutical DevelopmentAnalytical Problem Solving
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Equipment QualificationTemperature MappingWater System UtilitiesEnvironmental MonitoringRisk AssessmentProtocol WritingReport WritingAnnual Product ReviewsValidationGood Engineering Practices
Soft Skills
Excellent Writing SkillsInterpersonal SkillsConflict Resolution SkillsAnalytical SkillsProactive Problem Solving
Certifications & Qualifications
Four-Year College Degree in Chemical EngineeringChemistryBiochemistry
Industry Keywords
Pharmaceutical ManufacturingICH GuidelinesNational RegulationsInternational Regulations
About the role
Key responsibilities & impact- Lead and assist in Quality Assurance-related projects and day-to-day quality activities
- Improve the efficiency and effectiveness of engineering-related quality systems
- Generate, review, and approve equipment qualification documents
- Generate, review, and approve temperature mapping documents
- Generate, review, and approve water system utilities documents
- Generate, review, and approve environmental monitoring documents
- Generate, review, and approve risk assessments
- Generate, review, and approve cleaning documents
- Write protocols and reports
- Prepare Annual Product Reviews
- Provide guidance and leadership where appropriate
Requirements
What you’ll need- Four-year college or university program certificate in Chemical Engineering, Chemistry, Biochemistry, or related scientific field
- 6 years’ experience in Pharmaceutical Development and/or Manufacturing Operations
- Knowledge of current Good Manufacturing Practices, ICH Guidelines, and other pertinent national and international regulations
- Excellent writing, interpretive, presentation, and interpersonal skills
- Conflict resolution skills
- Understanding of equipment qualification and validation
- Good knowledge of good engineering practices and pharmaceutical manufacturing
- Analytical skills with the ability to function with interdisciplinary teams
- Proactive approach to problem solving and resolution
Benefits
Comp & perks- 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service
- Accident Plan
- Critical Illness
- Dental Insurance
- Disability Insurance
- Employee Assistance Program
- Flexible Spending Account
- Health Insurance PPO/HSA
- Hospital Indemnity Plan
- ID Theft
- Life Insurance
- Paid Parental Leave
- Tuition Reimbursement
- Wellness Program
- Vacation – Three Weeks 1st Year
- Vision Insurance