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Benefits offered by this job
Health and welfare benefits
401(k) participation
Dental and vision coverage
Job summary
A leading workforce solutions provider is seeking a Document Controller in Indianapolis. The role involves managing the document control lifecycle for QA documentation in compliance with industry regulations. Candidates should have a minimum of 4 years of experience in a regulated pharmaceutical environment and expertise in using Veeva QualityDocs. Strong attention to detail, communication skills, and the ability to work independently are essential for success in this role.
Qualifications
Minimum of 4 years of experience in document control within a GxP environment.
Proven ability to manage controlled documents independently.
Demonstrated hands-on experience supporting inspections and audits.
Responsibilities
Manage the end-to-end document control lifecycle for QA documentation.
Provide expertise on document control standards and processes.
Coordinate documentation routing through review and approval workflows.
Skills
Document control management
Quality Assurance (QA)
Attention to detail
Communication skills
Organizational skills
Cross-functional collaboration
Education
Bachelor’s degree or equivalent experience
Tools
Veeva QualityDocs
Job description
A leading workforce solutions provider is seeking a Document Controller in Indianapolis. The role involves managing the document control lifecycle for QA documentation in compliance with industry regulations. Candidates should have a minimum of 4 years of experience in a regulated pharmaceutical environment and expertise in using Veeva QualityDocs. Strong attention to detail, communication skills, and the ability to work independently are essential for success in this role.