Validation Specialist

Key Responsibilities Develop and execute validation protocols (IQ/OQ/PQ, process validation, cleaning validation)

Author validation final reports and ensure timely completion

Lead validation risk assessments and ensure compliance with GMP/GAMP requirements

Investigate deviations and support CAPA implementation

Coordinate with cross‑functional teams (QA, Engineering, Manufacturing)

Maintain and update Validation Master Plans (VMP)

Qualifications & Experience Degree in Engineering, Life Sciences, Biotechnology, or related field

4 – 8 years of validation experience in pharmaceutical or biotech manufacturing

Strong knowledge of GMP, GAMP, and ICH guidelines

Excellent documentation, communication, and problem-solving skills