Quality Assurance Specialist

Masis Professional Group; Easton (Northampton County); On-site; USD 65,000 - 70,000; Full time

Job summary

A leading pharmaceutical firm seeks a Quality Assurance Associate in Easton. This contract role involves driving compliance and supporting critical product production. Responsibilities include ensuring regulatory compliance, managing documentation, and leading audit preparations. Required qualifications include a bachelor's degree in a relevant field and some experience in the regulated industry. The job promotes a proactive quality culture and offers a competitive pay range.

Qualifications

• 0-2 years of experience in the pharmaceutical or related regulated industry.
• Deep understanding of cGMPs and regulatory standards.
• Ability to conduct investigations with sound quality decisions.

Responsibilities

• Provide documentation and compliance support to meet regulatory requirements.
• Manage multiple priorities and provide leadership to team members.
• Maintain oversight of the PAS-X system for audit readiness.

Skills

Compliance understanding

Problem-solving

Cross-department collaboration

Communication skills

Education

Bachelor’s degree in a scientific or technical field

Tools

Microsoft Outlook

Microsoft Excel

Microsoft Word

Job description

Masis Professional Group provided pay range

This range is provided by Masis Professional Group. Your actual pay will be based on your skills and experience – talk with your recruiter to learn more.

Base pay range

$65,000.00/yr - $70,000.00/yr

Join a fast-growing Pharmaceutical Manufacturing site in a long-term contract role as a Quality Assurance Associate. In this position, you’ll play a vital role in driving compliance, elevating operational standards, and supporting the production of critical care products that impact patients worldwide!

Job Summary

Strive to proactively drive the Quality culture at the site and promote cGMP activities. This person will work hands‑on with the responsibility of ensuring compliance, improving practices, and qualifying/validating new processes with company strategic goals as a guide.

Responsibilities

• Provide documentation and compliance support to meet Global Regulatory Requirements for licensed products.
• Partner with cross-functional departments to address GMP requirements in validation, investigations, complaints, procedure updates, and change control.
• Manage multiple priorities while providing leadership, guidance, and feedback to team members.
• Drive packaging OEE (Overall Equipment Effectiveness) initiatives.
• Support qualifications, deviations, customer complaints, investigations, and systems compliance.
• Maintain oversight of the PAS-X system and ensure 24/7 audit readiness.
• Support regulatory audits with thorough preparation and follow‑through.
• Lead document control activities to ensure accuracy, consistency, and compliance.

Education & Experience

• Bachelor’s degree or higher in a scientific, quality assurance, or technical field.
• 0-2 years of experience in the pharmaceutical or related regulated industry, including compliance and project management.
• Deep understanding of cGMPs, regulatory standards, and industry best practices.
• Ability to conduct investigations, interpret regulations, and make sound quality decisions.
• Exceptional verbal and written communication skills with the ability to collaborate across departments and leadership levels.
• Proficiency in Microsoft Outlook, Excel, Word, and other web-based systems.
• Strong problem‑solving skills with the ability to lead projects and deliver timely results.

Job Types: Contract, Temp-to-hire

Seniority level

Not Applicable

Employment type

Contract

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing