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Document Control Specialist Rochester, NY

Job in City of Rochester, Rochester, Monroe County, New York, 14602, USA
Listing for: Akkodis
Full Time position
Listed on 2026-01-01
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 22 - 34 USD Hourly USD 22.00 34.00 HOUR
Job Description & How to Apply Below
Position: Document Control Specialist Job in Rochester, NY:
Location: City of Rochester

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This range is provided by Akkodis. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$22.00/hr - $34.00/hr

Contract Pay Rate Range: $ per hour based on experience, education, geographic location and other factors.

Please no 3rd party or c2c candidates

Key Responsibilities of the Document Control Specialist Job in Rochester, NY
  • Administer and maintain the Document Control System (electronic and paper-based).
  • Manage document lifecycle including creation, review, approval, distribution, revision, and archival.
  • Ensure compliance with 21 CFR Part 11, 21 CFR 820, and ISO 13485 requirements.
  • Process Document Change Orders (DCOs), Deviations, and CAPAs.
  • Support internal and external audits by providing accurate and timely documentation.
  • Collaborate with cross-functional teams (QA, RA, R&D, Manufacturing) to ensure documentation supports regulatory and operational needs.
  • Train employees on document control procedures and systems.
  • Monitor and report on document control metrics and compliance status.
  • Maintain Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR).
Qualifications of the Document Control Specialist Job in Rochester, NY
  • Associate’s or Bachelor’s degree in a related field (Life Sciences, Quality, Regulatory Affairs preferred).
  • 2+ years of experience in document control within an FDA-regulated environment.
  • Proficiency with electronic document management systems (e.g., Master Control, Agile, Veeva).
  • Strong understanding of FDA regulations, ISO standards, and cGMP practices.
  • Excellent organizational skills and attention to detail.
  • Strong communication and interpersonal skills.
  • Ability to work independently and manage multiple priorities.
Preferred Skills
  • Experience supporting FDA inspections or ISO audits.
  • Familiarity with validation documentation and quality system records.
  • Knowledge of risk management and change control processes.

For more information or to be considered for the Document Control Specialist Job in Rochester, NY please contact Thomas McCarthy at

Equal Opportunity Employer/Veterans/Disabled

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Disclaimer:
These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client.

The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

  • California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance

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