Regulatory Document Coordinator - NIH
global solutions networkBethesda, MD
Regulatory Document Coordinator - NIH
global solutions networkBethesda, MD
2 days ago
Industries
Research and Development in Biotechnology (except Nanobiotechnology)Biological Product (except Diagnostic) ManufacturingElectromedical and Electrotherapeutic Apparatus ManufacturingAbout the role
Global Solutions Network (GSN), a federal government contracting firm, presents this full time, long-term position supporting GSN's customer at the National Institutes of Health (NIH). This position provides a competitive salary and comprehensive benefits. If interested, please provide an up-to-date resume.
Responsibilities:
1) Document Lifecycle Management The contractor staff shall manage the full lifecycle of Standard Operating Procedures (SOPs), Work Instructions (WIs), and Training Modules for Division of Facilities Operations and Maintenance (DFOM) Aseptic Processing Facilities (APF) and Biosafety Level (BSL) operations, including: Initial creation and drafting of new SOPs, WIs, and Training Modules in accordance with DFOM templates and formatting standards. Coordination of periodic review cycles to ensure documents remain current and technically accurate. Management of the revision process, including tracking requested changes and incorporating approved edits. Facilitation of the approval process, ensuring required approvers review and sign off within established time-frames. Management of distribution to ensure approved documents reach relevant personnel (see Requirement Area 3 for controlled distribution specifics). Management of document retirement and expiration, including archival of superseded or obsolete documents. 2) Document Control and Records Management The contractor staff shall utilize the NIH document control system that ensures compliance with organizational and regulatory record keeping requirements, including: Maintenance of detailed version control records for all SOPs, WIs, and Training Modules. Tracking of authorship for each document and revision. Maintenance of complete revision history for each controlled document. Tracking of approval status (pending, approved, rejected, returned for revision) for each document in the workflow. Recording and monitoring effective data for all approved documents. Monitoring of document expiration timelines and proactive initiation of review or archival processes as review/expiration dates approach. 3) Cross-Functional Review Coordination and Controlled Distribution The contractor staff shall coordinate document review activities and manage controlled access to current documentation, including: Coordination of cross-functional reviews involving relevant subject matter experts and stakeholders to ensure document accuracy. Verification that document content is consistent with current DFOM policies and procedures. Verification that document content aligns with applicable industry standards and regulatory requirements. Oversight of controlled distribution processes to ensure that only the most current, approved versions of documents are accessible to relevant personnel. Removal or restriction of access to superseded or expired document versions. 4) Personnel Training Management and Compliance Tracking The contractor staff shall track and manage personnel training status in direct linkage with the document control system, including: Linking of Training Modules to the specific SOPs and WIs they support. Tracking of individual employee training status against required modules. Monitoring to ensure all employees complete required training within designated time-frames. Maintenance of up-to-date, auditable training records for all applicable personnel. Generation of compliance reports summarizing training completion status across DFOM/APF/BSL personnel. Support of internal and external audits by providing documentation of employee qualifications and training adherence upon request.
Qualifications:
Bachelor's degree in a relevant field. Experience working biomedical laboratory settings. Demonstrated knowledge of regulatory documents related to Good Manufacturing Practice. Strong organizations, written, and interpersonal skills.
Benefits:
Medical, Dental, & Vision Coverage Paid Time Off and Paid Holidays 401K/Profit Sharing Plan Flexible Spending Accounts (Healthcare & Dependent Care) Pretax Parking & Transportation Plan Short-Term & Long-Term Disability Insurance Life & AD&D Insurance Professional Development/Education Employee Referral Bonuses Employee Discount Program Merit Bonuses Employee Assistance Program Travel Assistance Program Global Solutions Network, Inc. (GSN) is an Equal Employment Opportunity (EEO) employer. It is the policy of the GSN to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected US veteran or disabled status, or genetic information.
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JOB OVERVIEW
Experience level
Manager
Location
Bethesda, MD
Occupation
Regulatory Affairs Specialists
Industry
Research and Development in Biotechnology (except Nanobiotechnology)
Posted
2 days ago
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