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# Reagent Change Specialist

- **Company:** System One
- **Location:** Oro Valley, AZ, United States
- **Experience:** Experienced
- **Salary:** $59,238.0
- **Contract:** Temporary to permanent
- **Skills:** Agile Methodology, Document Management Systems, Microsoft Office, SAP (Applications), Gsuite, Software Version Control
- **Published:** June 5, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=a3d8080c3e173538

## About the Role

Do you have experience in Technical writing within manufacturing?, Do you have a Bachelor's degree?, * Bachelor's Degree in a scientific, manufacturing, supply chain, or related discipline.

 * 4+ years of experience in production, manufacturing, supply chain, quality, or a related field; Master's Degree with 2+ years of relevant experience preferred.
 * Strong understanding of scientific principles and manufacturing processes.
 * Advanced technical writing and documentation skills.
 * Excellent verbal and written communication abilities.
 * Strong organizational and time management skills.
 * Ability to work independently and collaboratively across functions.
 * Proficiency with Google Suite, Microsoft Office, Agile, EtQ, SAP, experience managing document control and change management processes.
 * Experience in GLP, cGMP, or ISO-regulated environments preferred.

## Description

* Coordinate and manage change control activities related to supplier product/process changes, CAPAs, non-conforming events, product obsolescence, and continuous improvement initiatives.
 * Partner with cross-functional stakeholders to assess change requirements, prioritize implementation activities, and ensure compliance with quality and regulatory standards.
 * Update and revise documents including Work Instructions, Operating Procedures, Production Documents, Temporary Deviations, Stability & Surveillance Memos, Technical Assessments, Protocols, and Reports using current templates and revision controls.
 * Facilitate stakeholder review and approval processes, track approvals, and address reviewer comments.
 * Support preparation of Change Control Board (CCB) requests and coordinate implementation activities with the Change Management Office (CMO).
 * Participate in cross-functional change control review teams as needed.
 * Adhere to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP), ensuring compliance with quality systems and regulations.
 * Collaborate with cross-functional teams, support continuous improvement initiatives, and contribute to team and departmental meetings.
 * Perform additional duties as assigned.


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