Mentor Technical Group
Validation Specialist – Biotech Downstream Process Equipment
Location not given · Full-time
Posted · Listed from JazzHR
About the job
Key Responsibilities:
Develop, review, and execute validation protocols (IQ, OQ, PQ) for downstream process equipment.
Perform risk assessments, gap analyses, and validation reports for new and existing equipment.
Collaborate with engineering, QA, and operations teams to ensure equipment meets regulatory requirements.
Support commissioning and qualification activities for bioprocess systems, including filtration, chromatography, and centrifugation equipment.
Review and approve validation documentation, SOPs, and change controls.
Identify and implement continuous improvement initiatives in validation processes.
Support regulatory inspections and audits, providing required validation documentation.
Qualifications:
Bachelor’s degree in Biotechnology, Biochemistry, Chemical Engineering, or related field.
Minimum 3–5 years of experience in validation of biotech downstream process equipment.
Strong knowledge of cGMP, FDA, and ICH guidelines.
Experience with IQ/OQ/PQ protocols and validation documentation.
Familiarity with downstream processes such as chromatography, filtration, and centrifugation.
Excellent problem-solving, communication, and organizational skills.
Preferred Qualifications:
Advanced degree in relevant scientific field.
Experience in a multi-site or global biotech environment.
Knowledge of computerized systems validation (CSV) and automated process control systems.
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