Sas Programming Jobs in Rochester, NY (NOW HIRING)

Position Summary
The Validation Specialist is responsible for supporting and executing validation and qualification activities for manufacturing processes, equipment, utilities, and facilities in a regulated environment. This role manages validation projects or discrete project components with limited supervision and ensures all activities are conducted in accordance with current Good Manufacturing Practices (cGMP), applicable regulatory requirements, and internal procedures.
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Essential Duties and Responsibilities
Validation Execution & Compliance
Develops the protocols in your functional area (process validation, sterile processes, cleaning validation)
Executes, and supports equipment and process qualification and validation protocols (e.g., IQ/OQ/PQ) for manufacturing, packaging, and facility systems.
Ensures validation activities are appropriately scoped, planned, and executed within project timelines, including resource and documentation requirements.
Performs sampling of in-process materials and environmental/cleaning verification (e.g., surface swabbing) in accordance with approved protocols.
Analyzes validation data using appropriate statistical and scientific methods to assess process capability and compliance.
Reviews and compiles supporting documentation (e.g., batch records, certificates of analysis, equipment logs).
Investigates deviations and exceptions, contributes to root cause analysis, and supports implementation of corrective and preventive actions (CAPA).
Determines and documents validation conclusions based on data, observations, and investigation outcomes.
Collaborates cross-functionally with Operations, Engineering, Quality Assurance, Quality Control, and Technical Services to ensure alignment and compliance.
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Documentation & Reporting
Authors validation protocols, reports, and supporting documentation for facilities, equipment, utilities, cleaning processes, and manufacturing operations.
Prepares summary and closeout reports in accordance with internal procedures and regulatory expectations.
Maintains validation documentation in an organized and inspection-ready state to support internal audits and regulatory inspections.
Ensures all validation deliverables are completed, reviewed, and archived in compliance with document control procedures.
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Continuous Improvement & Compliance Enhancement
Maintains current knowledge of regulatory expectations (e.g., FDA, cGMP) and industry best practices.
Evaluates existing validation and operational processes; identifies and implements improvements to enhance efficiency, quality, and compliance and improves procedures consequently.
Supports change control activities and ensures validation impact assessments are completed appropriately
Implements the CAPA (Corrective Actions & Preventive Actions) assigned to you, and supports site CAPA implementation 
Promotes the effective use of technology and systems to improve validation processes.
Provides training and guidance to stakeholders on validation processes and procedural updates.