QA Specialist 3, QA Enabling Functions - Quality Control

Jasper Products Inc; United States; Remote; USD 60,000 - 90,000; Full time

Job summary

An established industry player in life sciences is seeking a QA Specialist 3 to join their Quality Assurance team. This remote role is vital for ensuring products and processes meet regulatory standards and quality expectations. The ideal candidate will have a Bachelor’s degree in Life Sciences and 2-4 years of QA experience, particularly in documentation review and GMP compliance. You will be responsible for overseeing QC processes, conducting investigations, and maintaining communication with cross-functional teams. This is a fantastic opportunity to contribute to innovative solutions that improve lives while advancing your career in a supportive environment.

Qualifications

• 2-4 years of QA experience with proven documentation review skills.
• Strong understanding of GMP and regulatory requirements.

Responsibilities

• Perform QA reviews of floor activities in the QC laboratory.
• Review and approve QC documentation including test records and investigations.

Skills

QA documentation review

GMP compliance

Root Cause Analysis

CAPA implementation

Communication skills

Education

Bachelor’s degree in Life Sciences

Job description

QA Specialist 3, QA Enabling Functions - Quality Control

Jasper Products Inc, United States

2 days ago - Be among the first 25 applicants

Job Overview

Jasper Products, LLC is a global leader in life sciences, operating across five continents. We value talented people working together to devise ideas that help businesses and improve lives. We offer our team members ownership of their careers and encourage innovation and teamwork to achieve our mission.

We are seeking a QA Specialist 3, QA Enabling Functions to support our Quality Assurance team remotely. This role is crucial in ensuring our products and processes meet regulatory standards and quality expectations.

Key Responsibilities

• Perform QA reviews of floor activities in the QC laboratory.
• Review and approve QC documentation including test records, investigations, stability reports, and environmental monitoring.
• Oversee deviation investigations, discrepancy reports, and CAPA implementation.
• Ensure QC processes comply with GMP and regulatory standards.
• Maintain and assist with training on quality procedures.
• Handle investigations and change controls related to QC.
• Review and approve master documents related to QC.
• Apply Root Cause Analysis tools for record closure.
• Oversee Quality Change Requests for lab service changes.
• Develop and revise SOPs, forms, and specifications.
• Coordinate with cross-functional teams and maintain good communication.
• Perform project tasks and additional duties as assigned.

Minimum Requirements

• Bachelor’s degree in Life Sciences or related field.
• 2-4 years of QA experience, with proven documentation review skills.
• Strong understanding of GMP and regulatory requirements.
• Excellent communication and collaboration skills.
• Experience with Root Cause Analysis and CAPA is preferred.
• Ability to manage multiple tasks efficiently under supervision.

Additional Information

Level: Mid-Senior level

Employment Type: Full-time

Job Function: Quality Assurance