Manager, Document Control (QA Operations)

Forge BiologicsColumbus, OH
Onsite

About The Position

The Manager, Document Control - QA Operations leads the Document Control team in the compliant and efficient management, issuance, and maintenance of controlled documents utilizing an Electronic Quality Management System. Supporting manufacturing, quality assurance, quality control, and related operations, this role ensures effective Document Control and Records Management processes while driving continuous improvement and cross-functional collaboration.

Requirements

  • 8+ years of experience in Document Control, Quality Systems, Quality Writing, or a related role within a GMP-regulated environment supporting manufacturing and/or laboratory operations.
  • Experience managing cross-functional projects and stakeholder deliverables.
  • Experience using an Electronic Quality Management System (eQMS), preferably Veeva Vault or a comparable document management platform.
  • Strong written communication, organization, and project management skills, with the ability to present technical documentation clearly to internal and external stakeholders.
  • Previous experience leading, mentoring, or training employees and/or peers.
  • Ability to manage competing priorities in a fast-paced, deadline-driven environment while maintaining accuracy, completeness, and compliance.
  • Proficiency with Microsoft Office applications, including Outlook, Teams, Word, Excel, and PowerPoint.
  • Ability to work flexible hours, including evenings, weekends, and holidays to support manufacturing production schedules.

Nice To Haves

  • Associate’s or Bachelor’s Degree.
  • Proficiency with Project Management software (Smartsheet).
  • Formal training in technical writing, instructional design, or regulatory documentation.
  • Advanced skills in Microsoft Word formatting, styles, and templates.
  • Familiarity with CDMO operations and client-driven project timelines.
  • Strong interpersonal skills with the ability to influence and coach SMEs and stakeholders.
  • Experience supporting documentation teams through regulatory inspections (e.g., FDA, EMA).

Responsibilities

  • Provide leadership through effective communication, consistent coaching, reinforcing accountability, training, and development while removing roadblocks to support team execution.
  • Establish clear team goals, priorities, ownership, and objectives aligned with site strategy while managing team member performance, development, accountability, and growth through regular coaching and feedback.
  • Serve as the subject matter expert for the document management system, including eQMS/Veeva Vault functionality, document authoring, revision workflows, and controlled document lifecycle processes.
  • Evaluate, approve, and manage document change controls in the eQMS, assessing operational impact and ensuring alignment with internal procedures and applicable regulatory requirements.
  • Oversee issuance of controlled documents, including batch records, labeling, forms, and logbooks, to Operations and Quality Control departments while ensuring accuracy, traceability, and compliance.
  • Author, review, and approve controlled documentation, including Standard Operating Procedures (SOPs), Work Instructions, and related documents.
  • Oversee administration of eQMS stations in manufacturing areas to ensure required procedures, forms, and reference documents are current, available, and controlled.
  • Develop, monitor, and report metrics and key performance indicators for document change requests, document change controls, controlled copies, and periodic reviews to support timely stakeholder evaluation and document effectiveness.
  • Collaborate with cross-functional teams, SMEs, and stakeholders to identify, lead, and implement process improvements that enhance document control efficiency, compliance, and procedural alignment.
  • Support periodic maintenance, upgrades, and validation activities for the document management system, including related procedure updates.
  • Provide documentation support for regulatory inspections and internal audits, ensuring documentation readiness, accessibility, and compliance.

Benefits

  • Health, dental and vision insurance start your first day – with 90% of premiums covered for you and your family.
  • A competitive paid time off plan
  • 12 weeks of fully paid parental leave
  • Annual bonus opportunities for all full-time team members.
  • 401(k) with company match
  • Special employee discounts, including childcare and dependent care savings.
  • Onsite fitness facility at The Hearth.
  • Mental health counseling and financial planning services through our Employee Assistance Program.
  • Employer-paid short and long-term disability coverage
  • A fully stocked kitchen with free snacks and beverages
  • Ongoing professional development resources, training, and mentorship programs
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service