Avet Pharma is hiring for the position of Director, Quality Assurance at its facility in East Brunswick, New Jersey, USA.

This is a great opportunity for experienced pharmaceutical quality professionals who have strong knowledge of cGMP, FDA regulations, quality systems, audits, CAPA, investigations, and compliance management.

Position Details

Company: Avet Pharma

Job Title: Director, Quality Assurance

Location: East Brunswick, New Jersey, USA

Department: Quality Assurance

Industry: Pharmaceutical Manufacturing

Job Type: Full-Time

Job Responsibilities

The selected candidate will be responsible for:

Managing Quality Management Systems (QMS)

Ensuring compliance with cGMP, FDA, and DEA regulations

Leading regulatory inspections and audits

Handling batch disposition and quality investigations

Managing CAPA programs and compliance initiatives

Overseeing supplier qualification and validation activities

Working closely with Manufacturing, Engineering, R&D, and Regulatory Affairs teams

Driving continuous quality improvement programs

Required Qualifications

Strong experience in Pharmaceutical Quality Assurance

Knowledge of cGMP and FDA regulations

Experience with audits and regulatory inspections

Understanding of CAPA, investigations, and validation processes

Excellent leadership and communication skills

Why Join Avet Pharma?

Leadership role in a growing pharmaceutical company

Opportunity to work with global quality standards

Career growth and professional development

Collaborative and innovative work environment

How to Apply

Interested candidates can apply through the official Avet Pharma Careers website.

https://avetpharma.com/careers

FAQs

1. What is the job location?

The position is based in East Brunswick, New Jersey, USA.

2. What department is hiring?

The opening is in the Quality Assurance Department.

3. What regulations should candidates know?

Candidates should have knowledge of cGMP, FDA, and DEA regulations.

4. Is leadership experience required?

Yes, this is a senior-level position requiring strong leadership and quality management experience.

5. What are the main responsibilities?

The role includes managing quality systems, audits, investigations, CAPA programs, compliance activities, and regulatory inspections.