QC Lab Equipment Specialist II — Calibration & PM Leader

Kindeva; Bridgeton (MO); On-site; USD 75,000 - 110,000; Full time

Job summary

Kindeva is seeking a QC Specialist-Lab Equipment to drive calibration/PM programs and support cGMP laboratory operations. You will serve as a system administrator for lab software and provide technical support for equipment selection and validation initiatives.

The role requires strong analytical capabilities, experience with Empower CDS, and adherence to regulatory standards in a fast-paced pharmaceutical environment. On-site work in Bridgeton, MO is expected.

Qualifications

• Bachelor of Science in Chemistry.
• 5+ years in pharmaceutical laboratory operation and equipment maintenance.
• Knowledge of 21 CFR 210/211.
• Understanding of lab equipment and analytical techniques.
• Excellent analytical and investigation skills.
• Experience with Empower Chromatographic Data System and instrument software.
• Fluent in English (spoken and written).

Responsibilities

• Performs calibration/verification or PM per established procedures.
• Reviews calibration/verification or PM data for proper calibration.
• Maintains calibration records and certificates of standards.
• Maintains calibration standards or test equipment.
• Maintains records of service contractor and approves procedures.
• Ensures lab equipment procedures meet USP/NF/EP regulatory requirements.
• Notifies equipment owner and QA of discrepancies.
• Maintains Laboratory Equipment Master List and inspection readiness.
• Interprets data for accuracy, precision, trends and CGMP impact.
• Applies techniques and procedures; recommends improvements.
• Coordinates and supports laboratory equipment training.
• Supports SOP revisions, change controls, validation/qualification reviews.

Skills

Analytical skills

Leadership

Lean Six Sigma

English fluency

Education

Bachelor of Science in Chemistry

Tools

Empower Chromatographic Data System

Job description

Kindeva is seeking a QC Specialist-Lab Equipment to drive calibration/PM programs and support cGMP laboratory operations. You will serve as a system administrator for lab software and provide technical support for equipment selection and validation initiatives.

The role requires strong analytical capabilities, experience with Empower CDS, and adherence to regulatory standards in a fast-paced pharmaceutical environment. On-site work in Bridgeton, MO is expected.