Junior Equipment Validation Engineer

United Consulting Hub; United States; Sur place; USD 50 000 - 70 000; Plein temps

Résumé du poste

A consulting firm in life sciences seeks a motivated Equipment Validation professional to support validation activities ensuring compliance with regulatory standards like GMP. The role requires 0-2 years of experience in the pharmaceutical or life sciences industry, with responsibilities that include conducting operational and performance qualifications, preparing validation documents, and ensuring proper documentation for audits. This is a remote position.

Qualifications

• 0-2 years of experience in the pharmaceutical or life sciences industry.
• Support validation activities ensuring compliance with regulatory standards.

Responsabilités

• Conduct Operational Qualification (OQ) and Performance Qualification (PQ).
• Prepare and review validation documents: protocols, reports, SOPs.
• Perform risk assessments and ensure compliance with GMP and regulatory guidelines.

Formation

Pharmacy / Life Sciences / Biotechnology / Chemical Engineering

Description du poste

Job Summary

We are seeking a motivated Equipment Validation professional with 0-2 years of experience in the pharmaceutical or life sciences industry. The candidate will support validation activities to ensure that manufacturing and laboratory equipment operate consistently within predefined specifications and comply with regulatory standards like GMP.

Equipment validation ensures that equipment performs reliably and meets quality standards critical for product safety and compliance.

Key Responsibilities

• Operational Qualification (OQ)
• Performance Qualification (PQ)
• Prepare and review validation documents: Validation protocols, Reports and SOPs, Traceability matrices
• Perform risk assessments and identify critical process parameters
• Ensure compliance with: GMP (Good Manufacturing Practices), Regulatory guidelines (FDA, EMA, ISO), Calibration, Preventive maintenance, Re-validation activities
• Participate in deviation handling, CAPA, and change control processes
• Coordinate with cross-functional teams (QA, QC, Production, Engineering)
• Maintain proper documentation for audits and inspections

Required Qualifications

• Pharmacy / Life Sciences / Biotechnology / Chemical Engineering

Industry: Pharmaceutical / Life Sciences / Biotech

Location: Remote

Experience: 0 - 2 years