Validation Engineer

Job Title: Validation Engineer
Type: Contract
Location: Remote
Experience: 0–2 Years
Job Summary:
We are seeking a motivated and detail-oriented Validation Engineer to support qualification and validation activities for equipment, processes, utilities, and computerized systems within pharmaceutical and life sciences environments. This role provides an opportunity to develop practical experience in validation documentation, GMP compliance, and regulated manufacturing operations.
Key Responsibilities:
Assist with validation and qualification activities including:
Equipment qualification (IQ/OQ/PQ)
Process and cleaning validation
Utility and facility qualification
Computerized system validation activities
Support preparation, review, and execution of validation protocols and reports.
Ensure validation activities are performed in accordance with GMP and approved procedures.
Assist with validation lifecycle documentation and traceability.
Coordinate with QA, QC, Engineering, Manufacturing, and other cross-functional teams.
Collect, organize, and analyze validation data and test results.
Support investigation of validation deviations and implementation of CAPA.
Assist with audit preparation and regulatory inspection activities.
Maintain accurate validation records in accordance with Good Documentation Practices (GDP).
Required Skills:
Basic understanding of validation lifecycle concepts and documentation practices.
Knowledge of 21 CFR Part 11 and data integrity principles is preferred.
Familiarity with URS, DQ, FAT, SAT, IQ, OQ, and PQ concepts.
Strong analytical, organizational, and problem-solving skills.
Excellent attention to detail and technical documentation abilities.
Basic understanding of GMP and pharmaceutical quality requirements.

Work arrangement
Yes