Senior QC Analyst - GMP & Stability Focus

Curia Aalborg ApS; Camarillo (CA); On-site; USD 85,000 - 107,000; Full time

Benefits offered by this job

Generous benefits

Paid training

Career advancement

Education reimbursement

401K with matching

Learning platform

And more!

Job summary

Curia in Camarillo, CA is seeking a Quality Control Analyst III to support the manufacturing department and external customers. The role includes testing raw materials, in-process, end product, and stability samples, with emphasis on data evaluation and method validation.

Applicants should have a chemistry degree with significant related experience, familiarity with FDA GMP guidelines, and the ability to work flexible hours.

Qualifications

• Bachelor's degree or higher in Chemistry or related field with relevant experience.
• Experience in cGMP or GLP pharmaceutical environments is preferred.
• Ability to work nights/weekends as needed.

Responsibilities

• Perform complex testing and data evaluation (e.g., HPLC, ELISA).
• Troubleshoot equipment issues and communicate resolutions.
• Lead/participate in method validations and data trend evaluations.
• Support OOS investigations with root-cause analysis and CAPAs.
• Prepare SOPs, reports, and data summaries for management.

Skills

Verbal & written communication

Time management

Organizational skills

Problem solving

Team collaboration

Education

Bachelor's degree in Chemistry

Master's degree in Chemistry

PhD in Chemistry

Tools

Microsoft Office

Instrument systems knowledge

Job description

Curia in Camarillo, CA is seeking a Quality Control Analyst III to support the manufacturing department and external customers. The role includes testing raw materials, in-process, end product, and stability samples, with emphasis on data evaluation and method validation.

Applicants should have a chemistry degree with significant related experience, familiarity with FDA GMP guidelines, and the ability to work flexible hours.