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Associate Document Control Specialist

Associate Document Control Specialist

Tailored ManagementHillsboro, OR, United States
2 days ago
Job type
  • Temporary
Job description

Job Title : Associate Document Control Specialist

Location : 4625 NE Brookwood Parkway, Hillsboro, OR

Duration : 12-month contract (potential extension or conversion)

Pay Rate : $17.13 - $29.69 / hr (W2)

Benefits : Weekly pay, Medical, Dental, Vision coverage

Description

Responsibilities

  • Administer and manage Facilities Engineering records efficiently in accordance with Genentech quality policies.
  • Prepare, organize, and maintain documentation following established procedures.
  • Support departments with equipment and system documentation needs.
  • Coordinate system implementations and prepare supporting documentation.
  • Recommend process improvements and support workflow optimization.
  • Collaborate closely with Facilities Engineering and Quality teams across the Genentech / Roche network.
  • Maintain clear communication with management, team members, customers, and staff at other sites.
  • Perform duties within an FDA-regulated environment and ensure adherence to cGMP standards.
  • Manage Turn-Over Packages (TOPs) and Commissioning Packages for HTO site projects.
  • Take ownership of assigned responsibilities and proactively drive improvements.

Qualifications / Requirements

  • Proficient with Enterprise Content Management (ECM) systems for managing engineering documents, drawings, TOPs, and commissioning documentation.
  • Skilled in FileMaker Pro and EDMS applications (e.g., QualityDocs) for document control and change management.
  • Ability to develop, document, and maintain workflow processes and routine tasks.
  • Provide documentation support for investigations, discrepancies, and corrective actions.
  • Daily support to HTO personnel for documentation and system inquiries.
  • Ability to read, interpret, and produce Facilities Engineering documents.
  • Strong understanding of cGMP compliance.
  • Advanced documentation and organizational skills to maintain high-quality project files.
  • Effective technical writing skills for reports, procedures, and documentation updates.
  • Proficient in Microsoft Office, especially Word.
  • Ability to lift up to 50 lbs and adjust to overtime or schedule changes as needed.
  • Capable of working independently with minimal supervision.
  • Training Requirements

  • Complete all required cGMP training per departmental policies.
  • Complete all mandatory safety training.
  • Follow established procedures for on-the-job training.
  • Education / Training

  • High school diploma or GED; 1-3 years of related experience or equivalent education / experience.
  • Proficient with relational databases (MS Access, Oracle), project management systems (TouchPoint, Condor, Trackwise, MS Project), and data reporting tools (Excel, Access).
  • Basic knowledge of SAP or similar CMMS platforms.
  • Strong understanding of Windows environments; highly detail-oriented and thorough.
  • Strong customer service mindset with excellent interpersonal skills.
  • Strong analytical, organizational, and problem-solving abilities.
  • Excellent verbal and written communication skills.
  • #TM1

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