Document Control Specialist II — ISO 9001/NQA-1 (Onsite)

Actalent; Denver (CO); Sur place; USD 41 000 - 50 000; Temps partiel

Avantages offerts par ce poste

Medical

Dental and Vision

401(k) retirement plan

Résumé du poste

Actalent is seeking a Document Control Specialist II to administer and improve our quality documentation processes in a regulated manufacturing environment. You will control, revise, and retain quality records, drawings, and traveler files while ensuring ISO 9001 and NQA-1 compliance and audit readiness.

Based onsite in Westminster, CO, you will work with quality, manufacturing, and engineering teams, using Word, Excel, and Acrobat to manage documents and data analysis for quality metrics.

Qualifications

• Minimum 4 years in document control or records management in a regulated environment.
• Proficiency with Word, Excel and Adobe Acrobat for documentation and reporting.
• Experience reviewing engineering drawings and technical documentation for accuracy.
• Ability to maintain ISO 9001 and NQA-1 compliant documentation.
• Onsite work in Westminster, CO and US work authorization.

Responsabilités

• Administer revision-controlled quality documents and ensure accuracy and formatting.
• Control distribution of drawings, customer docs, travelers, and turnover packages.
• Manage records retention and retrievability per procedures and regs.
• Review documents before release or submittal for completeness and accuracy.
• Maintain compliant documentation systems and assist with audits.
• Chart and report quality data to support metrics and improvements.
• Collaborate with quality, manufacturing, and engineering teams to meet needs.

Connaissances

Document control

Records management

Microsoft Word

Excel

Adobe Acrobat

Engineering drawings

ISO 9001

NQA-1

Data analysis

Formation

High School Diploma or GED

Associate degree

Bachelor's degree

Outils

Microsoft Access

Database tools

Description du poste

Actalent is seeking a Document Control Specialist II to administer and improve our quality documentation processes in a regulated manufacturing environment. You will control, revise, and retain quality records, drawings, and traveler files while ensuring ISO 9001 and NQA-1 compliance and audit readiness.

Based onsite in Westminster, CO, you will work with quality, manufacturing, and engineering teams, using Word, Excel, and Acrobat to manage documents and data analysis for quality metrics.