Document Control Specialist

This role will work closely with members of the Document Control team and support routine daily operations for Document Management. The position will have some additional responsibility for documenting processes and supporting continuous improvement. This position will primarily be responsible for the processing and maintaining of GxP documents throughout their lifecycle with a focus on issuance and reconciliation. Responsibilities:Adhere to Standard Operating Procedures, Work Instructions, and other administrative practices.Manage activities associated with the Document Storage Room at both the GTMF and GTQC facilities.Organize and manage a high volume of documentation for archival in both electronic and paper-based processes.Assist with organizing and filing documents and records.Support issuance of controlled documentsAssist with reconciliation, retention, and archival of documents and records.Retrieve documentation from document storage and/or offsite archival upon internal customer requestProvide Document Control support in preparation of, during and after internal or external Audits/InspectionsProvide guidance and support based on knowledge of GDP and cGMP principles during daily activities.Communicate effectively to assess daily interdepartmental needs and priorities; escalate where appropriate.Requirements / Qualifications:Minimum of a Bachelor’s Degree in a science, engineering, or related discipline.1-4 years’ experience in Quality with experience in the pharmaceutical, biotech or other related life-sciences industry a plus. Experience in document control and electronic document management systems.Strong attention to detail and organizational skills, is required.Able to work independently, prioritize, and manage multiple tasks simultaneously.Demonstrates initiative and a strong sense of urgency.Proficient in MS Excel, Word, and PowerPoint.Effective teamwork and collaboration with internal and external SMEs.Knowledgeable in cGMP's and pharmaceutical industry regulations a plus.High ethical standards, good judgment, and professionalism.Company DescriptionThe Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire & Contract Consultants) and Retained Executive Search.

Salary : $34 - $36