Overview
Quality control consultant Jobs in Texas, United States at United Pharma Technologies Inc
Title: Quality control consultant
Company: United Pharma Technologies Inc
Location: Texas, United States
Job Title: Quality Control Consultant – Chromatogram Review
Location: Houston, TX | On-Site
Position Summary
We are seeking an experienced Quality Control Consultant to support a short-term, on-site engagement at a pharmaceutical, biotechnology, or other regulated life sciences facility in Houston, TX. The consultant will be responsible for performing detailed reviews of chromatograms and associated analytical data to ensure accuracy, completeness, data integrity, and compliance with applicable GMP, GLP, and regulatory requirements.
Key Responsibilities
- Conduct comprehensive on-site reviews of chromatograms and associated analytical data.
- Evaluate analytical results for accuracy, completeness, consistency, and compliance with approved procedures and applicable quality standards.
- Review chromatographic data for potential discrepancies, anomalies, data integrity concerns, deviations, and other quality issues.
- Document observations and findings clearly and accurately in accordance with site procedures.
- Collaborate with Quality Control, Analytical, Laboratory, and Quality Assurance teams to investigate and resolve identified issues.
- Ensure analytical data and chromatogram reviews align with applicable GMP, GLP, data integrity, and regulatory requirements.
- Support timely completion of assigned review activities within the scope and timeline of the consulting engagement.
- Work independently while maintaining effective communication with site stakeholders and laboratory personnel.
Qualifications
- Proven experience in Quality Control, Analytical Testing, or Laboratory Operations within the pharmaceutical, biotechnology, or other regulated industries.
- Strong hands-on experience with chromatogram review and analytical data evaluation.
- Familiarity with chromatographic techniques and analytical laboratory systems.
- Knowledge of GMP, GLP, data integrity principles, and applicable regulatory requirements.
- Experience identifying and documenting analytical discrepancies, deviations, and quality concerns.
- Strong attention to detail and excellent documentation skills.
- Ability to work independently and effectively in a short-term, on-site consulting environment.
- Excellent communication and collaboration skills.
Preferred Experience
- Experience reviewing data generated from HPLC, UPLC, GC, or other chromatographic techniques.
- Familiarity with laboratory data systems, electronic records, and applicable data integrity expectations.
- Experience supporting QC investigations, audit readiness, or quality remediation activities.
