Job Description
Job Description
Title : QA Associate I
Location : Frederick, MD
Duration : 6+ months on W2
Schedule : Wednesday to Saturday, 8:00 AM - 6:30 PM, Sunday to Wednesday - 8:00AM to 6:30PM
Payrate : $27 - $27.55/hr
Job Summary
We are seeking a detail-oriented QA Associate I to support Quality Assurance documentation and records management activities within a regulated pharmaceutical/manufacturing environment. This role is responsible for maintaining controlled documents, managing archival records, performing data entry, and ensuring documentation accuracy and compliance.
Key Responsibilities
- Create, maintain, and issue logbooks and controlled documents.
- File, scan, verify, and archive quality records and documentation.
- Maintain document archival systems and ensure records are easily retrievable.
- Perform accurate data entry and database updates.
- Support document control and records management processes.
- Review documentation for completeness and compliance.
- Assist with departmental projects and administrative tasks.
- Escalate compliance-related questions or issues to management.
- Support quality system activities in accordance with company procedures.
Required Qualifications
- High School Diploma or equivalent required.
- Strong attention to detail and organizational skills.
- Excellent data entry, typing, and computer skills.
- Ability to multitask and manage priorities effectively.
- Strong verbal and written communication skills.
- Experience with documentation, records management, or administrative support preferred.
Preferred Qualifications
- Bachelor's degree in a related field.
- Experience in pharmaceutical, biotechnology, medical device, GMP, FDA-regulated, or manufacturing environments.
- Document Control, Quality Systems, or QA documentation experience.