Document Review Specialist

Cayuga Milk Ingredients; City of Auburn (NY); On-site; USD 34,440 - 48,216; Full time

Job summary

Cayuga Milk Ingredients is seeking a Document Review Specialist to ensure timely review, verification, and reconciliation of production, processing, quality, and regulatory documentation within aseptic and dairy ingredient operations.

The role supports FDA regulations, PMO, LACF, SQF, HACCP, FSMA, cGMPs, and company quality standards while maintaining QA records in EDMS and supporting audits.

Qualifications

• Associate's degree in Food Science, Quality Assurance, Manufacturing or related field.
• Experience in document control, quality assurance, or regulated manufacturing.
• Strong knowledge of GDP, ALCOA+ and GMP principles.

Responsibilities

• Review Batch Production Records and related documentation for completeness and compliance.
• Verify required signatures, dates, and timestamps prior to product release.
• Maintain controlled document management systems and EDMS.
• Support FDA/SQF/USDA audits and regulatory compliance.
• Collaborate with Production and QA to resolve documentation discrepancies.

Skills

Attention to detail

Documentation control

Analytical thinking

Time management

Education

Associate's degree in Food Science/QA or related field

Bachelor's degree in Food Science or related (preferred)

Tools

eQMS/EDMS

Microsoft Office

Job description

Overview

Position Title: Document Review Specialist

Reports To: Sr. Quality Manager

FLSA Status: Non-exempt

Job Grade: 3

Pay Range: $24.50-$35.00

Date Revised: June 2026

The Document Reviewer Specialist is responsible for the timely review, verification, reconciliation, control, and administration of production, processing, quality, and regulatory documentation within Cayuga Milk\'s aseptic, ESL, and dairy ingredient manufacturing operations. This role serves as a critical member of the Quality Assurance team by ensuring all manufacturing and quality records are complete, accurate, compliant, and audit-ready prior to final quality review and product release.

Working closely with Production, Quality Assurance, Food Safety, Engineering, Maintenance, Laboratory, and Sanitation teams, the Document Reviewer Specialist maintains the integrity of the Quality Management System (QMS) through effective document control, batch record review, electronic records management, and regulatory compliance. This position supports compliance with FDA regulations, Grade "A" Pasteurized Milk Ordinance (PMO), Low Acid Canned Food (LACF) regulations (21 CFR Part 113), SQF Food Safety Code, HACCP, FSMA, GMPs, and company quality standards.

The Document Reviewer Specialist performs the detailed review and reconciliation of documentation; however, final product disposition and release authority remains with the Document Control Specialist, Quality Manager, or other designated Quality leadership.

Essential Duties & Responsibilities

Production Record Review & Verification

• Review Batch Production Records (BPRs), manufacturing records, packaging records, sanitation documentation, laboratory records, and quality documentation for completeness, accuracy, legibility, and compliance.
• Verify production documentation prior to product release review.
• Confirm all required signatures, initials, dates, timestamps, and verification activities are properly completed.
• Verify critical process parameters including:
• Time
• Temperature
• Pressure
• Flow rates
• Hold tube performance
• Scheduled process requirements

• Review aseptic processing documentation for compliance with FDA Low Acid Canned Food (21 CFR Part 113) regulations and Process Authority requirements.
• Compare production documentation against approved Master Manufacturing Records, scheduled processes, formulas, specifications, and work instructions.
• Identify missing documentation, calculation errors, omissions, deviations, or inconsistencies requiring correction.
• Collaborate with Production and QA personnel to resolve documentation discrepancies before records are finalized.
• Prepare complete documentation packages for Quality review prior to product disposition.

Document Control Administration

• Maintain the company\'s controlled document management system.
• Prepare, proofread, format, and process controlled documents.
• Maintain revision histories and document version control.
• Maintain Master Document Lists.
• Issue controlled documents throughout manufacturing departments.
• Remove obsolete documentation from circulation.
• Maintain document retention in accordance with company policy and regulatory requirements.
• Scan, file, organize, archive, and retrieve electronic and paper records.
• Support implementation and maintenance of Electronic Document Management Systems (EDMS).
• Ensure documents remain secure, confidential, and readily retrievable.

Quality Records Management

Maintain and review quality documentation including but not limited to:

• Batch Production Records
• Aseptic processing records
• Thermal processing records
• Laboratory testing records
• Environmental monitoring records
• Calibration records
• Preventive maintenance records
• Sanitation records
• CCP monitoring records
• HACCP records
• CAPA documentation
• Internal audit documentation
• Supplier approval records
• Product specifications
• Ingredient specifications
• Process Authority documentation
• Employee training records
• Validation and verification documentation
• Ensure all records are complete, accurate, legible, and retained according to company procedures.

Regulatory Compliance

Support compliance with:

• FDA Food Safety regulations
• 21 CFR Part 113 (Low Acid Canned Foods)
• Grade "A" Pasteurized Milk Ordinance (PMO)
• HACCP
• FSMA
• Current Good Manufacturing Practices (cGMPs)
• SQF Food Safety Code
• USDA requirements
• State regulatory agencies
• Customer-specific quality requirements
• Good Documentation Practices (GDP)
• ALCOA+ documentation principles

Audit Support

Provide documentation support during:

• SQF Certification Audits
• FDA inspections
• USDA inspections
• State regulatory inspections
• Customer audits
• Internal audits
• Third-party certification audits

Responsibilities include:

• Retrieving requested documentation
• Preparing audit files
• Organizing production records
• Reconciling documentation
• Supporting corrective action documentation
• Assisting with audit responses
• Ensuring records are inspection-ready

Continuous Improvement

• Track recurring documentation errors and trends.
• Recommend improvements to document control processes.
• Assist with development of standardized forms and templates.
• Support operator retraining through documentation trend analysis.
• Participate in continuous improvement initiatives related to documentation accuracy and compliance.
• Assist with implementation of electronic quality systems.
• Support special Quality and Operations projects.

Cross-Functional Collaboration

Work closely with:

• Production
• Quality Assurance
• Food Safety
• Laboratory
• Engineering
• Maintenance
• Sanitation
• Supply Chain
• Operations Leadership

to resolve documentation issues, investigate deviations, and improve documentation quality.

Qualifications

Education

Required

• Associate\'s degree in Food Science, Quality Assurance, Business Administration, Manufacturing Technology, or a related field.

Preferred

• Bachelor\'s degree in Food Science, Dairy Science, Quality Systems, Business Administration, or related discipline.

Equivalent combinations of education and experience may be considered.

Experience

Required:

• Minimum 2–3 years of experience in document control, quality assurance, manufacturing documentation, records management, or regulated manufacturing.

Preferred:

• Dairy manufacturing experience.
• Aseptic processing experience.
• Food manufacturing experience.
• Electronic Quality Management Systems (eQMS/EDMS).
• FDA-regulated manufacturing.
• Batch record review.
• Quality Management Systems.

Knowledge, Skills & Abilities

• Strong understanding of document control principles.
• Excellent organizational and time management skills.
• Exceptional attention to detail.
• Ability to identify documentation inconsistencies.
• Strong analytical and problem-solving skills.
• Ability to prioritize multiple tasks in a fast-paced manufacturing environment.
• Excellent written and verbal communication skills.
• Proficiency in Microsoft Office Suite (Excel, Word, Outlook, SharePoint).
• Experience with Electronic Document Management Systems preferred.
• Working knowledge of:
• GMPs
• HACCP
• SQF
• FSMA
• FDA regulations
• PMO
• LACF (21 CFR Part 113)
• Good Documentation Practices
• ALCOA+ principles
• Ability to maintain confidentiality of quality and manufacturing records.

Core Competencies

• Attention to Detail
• Accountability
• Integrity
• Organization & Planning
• Analytical Thinking
• Critical Thinking
• Continuous Improvement
• Teamwork & Collaboration
• Communication
• Adaptability
• Customer Focus
• Professionalism
• Dependability
• Quality Orientation
• Regulatory Compliance

Performance Expectations

Successful performance is demonstrated by:

• Accurate and timely review of production documentation.
• High-quality document reconciliation with minimal errors.
• Complete, compliant, and audit-ready production records.
• Timely identification and resolution of documentation discrepancies.
• Effective support of FDA, SQF, USDA, customer, and internal audits.
• Accurate maintenance of controlled documents.
• Compliance with Good Documentation Practices (GDP) and ALCOA+ principles.
• Timely completion of assigned document reviews.
• Continuous improvement of documentation accuracy and efficiency.
• Effective collaboration with Production and Quality teams.

Work Schedule

This position works a 12-hour rotating day shift (6:00 AM – 6:00 PM) on a rotating schedule of:

• 3 days on
• 2 days off
• 2 days on
• 3 days off

The schedule repeats continuously and includes weekends and holidays as scheduled.

Physical Requirements & Work Environment

• Ability to work throughout office, laboratory, warehouse, and manufacturing environments.
• Regular standing, walking, bending, reaching, climbing stairs, and navigating production areas.
• Exposure to cold, wet, humid, and noisy dairy manufacturing environments.
• Ability to wear required Personal Protective Equipment (PPE), including hairnets, beard nets, frocks, safety glasses, hearing protection, and slip-resistant footwear.
• Ability to lift up to 50 pounds independently and heavier items with assistance or reasonable accommodation.
• Ability to distinguish colors, read technical documentation, and accurately review handwritten and electronic records.
• Ability to work safely around operating production equipment while following all food safety and plant safety requirements.
• Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of the position.

Position Impact

The Document Reviewer Specialist plays a vital role in protecting product quality, food safety, regulatory compliance, and operational excellence by ensuring that every production and quality record is complete, accurate, and compliant before products advance through the quality review and release process. Through disciplined document review and effective document control practices, this position helps maintain the integrity of Cayuga Milk\'s Quality Management System and supports successful regulatory inspections, customer audits, and SQF certification.