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Document Control Specialist

Job in Princeton, Mercer County, New Jersey, 08543, USA
Listing for: TSR Consulting Services, Inc.
Full Time position
Listed on 2025-12-01
Job specializations:
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 30 - 31 USD Hourly USD 30.00 31.00 HOUR
Job Description & How to Apply Below

Overview

Job Title:

Document Control Specialist

Location:

100% onsite in Princeton Pike, NJ

Job

Base pay range: $30.00/hr - $31.00/hr

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

Direct message the job poster from TSR Consulting Services, Inc.

Responsibilities
  • Administer the document control system, ensuring accurate tracking, version control, and distribution of controlled documents.
  • Review, format, and process documents such as SOPs, policies, protocols, and reports for compliance with company standards and regulatory requirements.
  • Coordinate document review and approval workflows, ensuring timely completion and proper authorization.
  • Support internal and external audits by providing requested documentation and ensuring records are audit-ready.
  • Monitor document lifecycle, including periodic review, revision, and obsolescence.
  • Ensure compliance with industry regulations (e.g., FDA, EMA, ICH-GCP) and company policies.
  • Assist in the development and improvement of document control processes and systems.
  • Respond to document-related inquiries from internal teams and external partners.
Education

Bachelor’s degree in Life Sciences, Business Administration, or related field (or equivalent experience).

Qualifications
  • 2+ years of experience in document control, quality assurance, or regulatory affairs, preferably in a pharmaceutical, biotech, or medical device environment.
  • Advanced proficiency with MS Word
  • Familiarity with document management systems (e.g., Veeva, Master Control, SharePoint).
  • Strong attention to detail and organizational skills.
  • Excellent written and verbal communication skills.
  • Ability to work independently and collaboratively in a fast-paced, regulated environment.
  • Knowledge of regulatory requirements for documentation in the life sciences industry.
  • Preferred:
    Experience supporting FDA or other regulatory inspections.
  • Preferred:
    Certification in document control or quality management (e.g., ISO, ASQ).
  • Preferred:
    Advanced proficiency with electronic document management systems.
Seniority level
  • Entry level
Employment type
  • Contract
Job function
  • Analyst
Industries
  • Pharmaceutical Manufacturing
  • Biotechnology Research
  • Medical Equipment Manufacturing

Referrals increase your chances of interviewing at TSR Consulting Services, Inc. by 2x

Inferred from the description for this job Benefits
  • Medical insurance
  • Vision insurance
  • 401(k)

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