Laboratory Instrumentation and Validation Specialist
Serán BioScienceAbout the role
Supervisory Responsibilities
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Recruits, interviews, hires, and trains new staff in accordance with company procedures.
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Oversees daily workflow, assigns tasks, and manages resource planning.
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Provides constructive and timely performance evaluations.
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Handles discipline and termination of employee in accordance with company policy.
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Ensures team compliance with training requirements, safety programs and GMP expectations
Duties and Responsibilities
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Support data integrity, audit readiness, and lifecycle management of electronic laboratory systems and analytical equipment.
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Leads instrument onboarding, installation, qualification, and computer system validation (CSV) activities for new or modified laboratory equipment and software systems.
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Authors, reviews, and maintains validation documentation, ensuring alignment with GAMP and GxP expectations.
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Performs routine and non-routine troubleshooting of laboratory instruments to identify root causes, restore operation, and minimize downtime.
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Coordinate and oversees instrument repairs, preventive maintenance, and service activities with internal teams and external vendors.
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Supports calibration and metrology programs, including scheduling, documentation review, and management of out-of-tolerance events.
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Owns or contributes to deviations, investigations, CAPAs, and change controls related to laboratory equipment and computerized systems.
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Maintains and updates SOPs, work instructions, and related documentation to ensure compliance and operation consistency.
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Participates in internal and external audits, providing documentation, subject-matter expertise, and corrective action support.
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Manages vendor relationships, service contracts, and provides budgetary input for equipment lifecycle planning.
Required Skills and Abilities
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Experience supporting laboratory instruments in a QC or regulated laboratory environment.
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Familiarity with CSV, instrument qualification, and GMP documentation expectations.
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