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Our client, a leading non-profit, FDA-licensed biologics manufacturer in Massachusetts is seeking a Document Control Specialist for a 6-12 month temporary assignment. This onsite role in Mattapan, MA, offers $23/hour and standard 9-5 hours. The organization focuses on vaccine and biologic product development, production, and distribution nationwide.

Job Responsibilities:

Maintain site training program, ensuring assignments, completion, and documentation are current.Generate and distribute training compliance/status reports to site leadership.Issue, track, and reconcile controlled logbooks and forms for operational compliance.Perform records archiving, file clean-up, and high-volume document production.Support electronic document management system (EDMS) operations, including document issuance and change workflows.Assist with operational reporting by providing documentation status and training metrics.Support review and routing of completed records to Quality for archiving.

Candidate Qualifications:

Bachelor's degree or higher with minimum 2 years in document control, records management, or regulated/quality-compliance environment.Working knowledge of document control principles, version control, record retention, and traceability.Experience with electronic document management systems (MasterControl preferred) and Microsoft Office.Strong attention to detail, organizational skills, and ability to manage multiple deadlines.Excellent written and verbal communication, with ability to work independently and collaboratively.Preferred: experience with controlled logbooks, EDMS reporting, archiving, and inspection readiness.

Qualified and interested candidates are encouraged to apply today for immediate consideration.

A1441221ERM_1769100803 To Apply for this Job Click Here