Intern, Quality

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.

Job Description Summary

The Program

Par Health offers an 11-week internship program designed to provide an immersive experience in the pharmaceutical industry. As a Par Health Intern, you’ll have the chance to contribute to meaningful projects that align with your field of study. This program allows you to apply classroom knowledge in a real-world corporate setting while building valuable connections through networking opportunities across the organization.

Summary of Position

This role will support the Quality Unit in maintaining and continuously improving the site’s Quality Management System (QMS) in line with GMP, regulatory expectations, and internal standards. Working under the guidance of experienced Quality professionals, the intern will gain hands on exposure to key quality processes including document control, deviation management, CAPA tracking, change control, batch record review, and quality oversight of manufacturing and packaging operations.
This role is ideal for a motivated student seeking practical industry experience in a virtual, highly regulated environment. The intern will collaborate with cross functional teams, assist in routine quality activities, and contribute to small improvement projects designed to strengthen compliance and operational efficiency.

Job Description

Responsibilities

  Support quality documentation activities, including reviewing, organizing, and updating SOPs, batch records, and logbooks under supervision.

  Assist with quality investigations by gathering data, supporting root‑cause analysis, and helping track CAPA actions.

  Perform routine GMP checks, such as verifying documentation completeness, monitoring training compliance, and supporting audit or inspection preparation.

Minimum Requirements

Enrolled in bachelor’s degree program related to Science, ideally pharmaceuticals.

• Experience with MS Office, etc.
• Motivated self-starter, operates independently, etc.
• Strong communication skills, etc. 

Relationship with Others/Scope of Position

Interact with other team members and cross functionally as needed

DISCLAIMER:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.