Quality Documentation & Change Control Specialist

BD; Tempe (AZ); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

401(k)

Job summary

BD in Tempe, AZ is seeking a Contract Opportunity to manage change requests and related documentation in an EDMS. This fixed-term assignment ends December 28, 2028, with responsibilities spanning document creation, review, lifecycle management, and compliance.

The role requires strong English communication, attention to detail, MS Office proficiency, and the ability to operate independently in a fast-paced, regulated environment. Prior experience in FDA-regulated settings is preferred.

Qualifications

• High School Diploma or GED required
• Associate's or Bachelor's degree preferred
• Minimum of 1 year of experience in a documentation-related role, preferably in an FDA-regulated environment
• 1 to 3 years of relevant professional experience

Responsibilities

• Manage day-to-day administration of change requests in the EDMS
• Review and verify change request documentation for accuracy
• Create, edit, and maintain controlled documents
• Oversee full lifecycle of change requests from initiation to closure
• Track workload and key metrics to supervisors and project teams
• Collaborate with project teams and document owners to drive changes to completion
• Maintain compliance with regulatory and quality standards
• Support regulatory audits and inspections
• Identify and recommend process improvements

Skills

English proficiency

Attention to detail

MS Office

Organizational skills

Multi-tasking

Education

High School Diploma or GED

Associate/Bachelor's degree preferred

Tools

EDMS (MasterControl)

Teamcenter

PEGA

Job description

BD in Tempe, AZ is seeking a Contract Opportunity to manage change requests and related documentation in an EDMS. This fixed-term assignment ends December 28, 2028, with responsibilities spanning document creation, review, lifecycle management, and compliance.

The role requires strong English communication, attention to detail, MS Office proficiency, and the ability to operate independently in a fast-paced, regulated environment. Prior experience in FDA-regulated settings is preferred.