Document Control Specialist, QA
Pennington, New Jersey
Experience: 0
Category: Scientific & Clinical
Contractor Work Model: Onsite
Brand: System One
Job ID: 382107
Date Posted: 10/22/2026
Shortcut: http://jobs.systemone.com/Nskox1
Job Title: Document Control Specialist, QA
Location: Pennington, NJ
Type: Contract to Hire
Pay Rate: $31.00 per hour
Hours: Monday-Friday 9am-5pm
Overview:
Under the oversight of the Quality Assurance Leadership, this position is responsible for providing quality and operational oversight of Document Control, Records Retention, and Archive Management activities. The role works closely with site and global teams to ensure compliant documentation practices, effective records management, archival governance, and sustained inspection readiness
Responsibilities:
- Serve as Business Process Owner (BPO) and Subject Matter Expert (SME) for Document Control, Records Retention, and Archive Management processes.
- Oversee document lifecycle management, records retention, archival activities, and related systems to ensure compliance with GMP, quality, and regulatory requirements.
- Manage controlled document issuance and logbooks, records inventories, retention schedules, archival requests, record retrieval.
- Monitor process performance, maintain inspection readiness, and support audits through documentation management and SME participation.
- Collaborate with local and global cross-functional teams to ensure alignment with corporate standards and best practices.
- Maintain oversight of documents, records, and archive workflows, including reporting, periodic reviews, and system administration activities.
- Review of GMP records (such as production records, cleaning records, line clearance records, QC records etc.)
- Review executed validation documents and protocols
- Other duties as assigned
Requirements:
- Bachelor's degree preferred in Life Science, Science, or a Regulatory-related field, and/or equivalent experience.
- Minimum of 3-5 years within the GMP industry, including demonstrated experience providing quality oversight in a manufacturing and/or warehouse environment.
- Demonstrated ability to lead, influence, and communicate across multisite, multi-cultural teams.
- Capable of clearly explaining, coaching, and supporting cross functional teams through Document Management processes and best practices.
- Able to articulate and defend Document Control principles, rationale, and compliance expectations during internal and external audits.
- Strong understanding of GMP principles and expectations, with the ability to apply them effectively in daily operations.
- Proficient in Quality Systems processes, including their purpose, interdependencies, and execution in a regulated environment.
- Internal and external audit experience is preferred.
- Master Control experience is strongly preferred.
Ref: 558-Scientific
#M-3
#LI-MM1
Ref: #558-Scientific
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