On-site QA Auditor: Drive Compliance & Process Improvement

Altasciences; Scranton (Lackawanna County); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) match

Paid vacation & holidays

Sick leave

Telework when applicable

Job summary

Altasciences in Scranton, PA is seeking a QA Auditor to perform independent audits of trial-related activities and documents. You will ensure data recording and reporting meet protocol, SOPs, GxP, and regulatory requirements.

Under supervision, you will write inspection reports, communicate findings clearly, and participate in process improvement activities across departments. A strong background in chemistry/biochem/biology and GMP knowledge is essential.

Qualifications

• Bachelor degree in a relevant science field required.
• Experience with GMP, GLP, GCP regulatory expectations preferred.
• Strong attention to detail and documentation discipline.

Responsibilities

• Audit trial-related activities and documents for compliance with SOPs, GxP, and regulations.
• Prepare inspection reports and communicate findings to study teams.
• Evaluate responses to findings and support process improvement.
• Maintain QA records and study files with accuracy and timeliness.
• Assist in sponsor and internal audits and training as needed.

Skills

Auditing

Regulatory knowledge

Quality systems

Data review

Education

Bachelor degree in Chemistry/Biochemistry/Biology or equivalent

Job description

Altasciences in Scranton, PA is seeking a QA Auditor to perform independent audits of trial-related activities and documents. You will ensure data recording and reporting meet protocol, SOPs, GxP, and regulatory requirements.

Under supervision, you will write inspection reports, communicate findings clearly, and participate in process improvement activities across departments. A strong background in chemistry/biochem/biology and GMP knowledge is essential.