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Quality Assurance (QA) Associate

  • Quality Assurance (QA) Associate job type Posted on: Nov 04, 2026
  • Quality Assurance (QA) Associate experience level Lancesoft INC
  • Quality Assurance (QA) Associate employment type Frederick, Maryland
  • Quality Assurance (QA) Associate salary Salary: $27 per hour
  • Quality Assurance (QA) Associate employment type Onsite
  • Quality Assurance (QA) Associate salary Full-time

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Job Title :

Quality Assurance (QA) Associate

Job Type :

Full-Time

Job Location :

Frederick Maryland United States

Remote :

No

Jobcon Logo Job Description :

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.

Jobcon Logo Position Details

Posted:

Nov 04, 2026

Reference Number:

11745f17

Employment:

Full-time

Salary:

$27 per hour

City:

Frederick

Job Origin:

ziprecruiter

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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.

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