QA Specialist

Piper Companies; United States; Remote; USD 60,000 - 80,000; Full time

Job summary

Piper Companies is seeking a QA Specialist for a remote position with a global pharmaceutical company. The role involves overseeing quality assurance activities, reviewing deviations, and ensuring compliance with global regulations. Candidates should have a relevant bachelor's degree and at least two years of experience in a GMP regulated environment.

Benefits

Medical, Dental, Vision benefits

Qualifications

• Minimum 2 years of experience in a pharmaceutical or biotechnology GMP regulated environment.
• At least 2 years of experience with labeling review for global regulations.
• Experience with deviations, investigations, change controls, batch record review, and CAPAs.

Responsibilities

• Oversee quality assurance activities including label review and batch record review.
• Review and approve deviations, investigations, and change controls.
• Ensure timely closure of investigations and write CAPAs.

Skills

Organizational skills

Education

Bachelor’s degree in biology, chemical engineering, biochemistry, or related field

Job description

Join to apply for the QA Specialist role at Piper Companies.

Piper Health and Sciences is actively seeking a QA Specialist to work for a large global pharmaceutical company focusing on their consumer product line. This is a remote / work from home position.

Responsibilities for Quality Assurance (QA) Specialist:

• Oversee quality assurance activities including label review and batch record review for global product line.
• Review and approve deviations, investigations, bill of materials, and change controls.
• Ensure timely closure of investigations, assist with root cause analyses, oversee change controls, and write CAPAs.
• Assist in reviewing and revising process improvement plans.
• Review, draft, edit, and approve SOPs and specifications.

Technical Requirements for Quality Assurance (QA) Specialist:

• Bachelor’s degree in biology, chemical engineering, biochemistry, or related field.
• Minimum 2 years of experience in a pharmaceutical or biotechnology GMP regulated environment.
• At least 2 years of experience with labeling review for global regulations.
• At least 2 years of experience with deviations, investigations, change controls, batch record review, and CAPAs.
• Excellent organizational skills and proven experience working in a fast-paced environment.

Compensation & Benefits:

• Compensation: $32-36/hr based on experience.
• Full Benefits: Medical, Dental, Vision, etc.

This job opens for applications on 05/21/2025.