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 ProgramPar 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
The Legal Intern will support Par Health’s Legal Department across a variety of matters affecting a global pharmaceutical organization. This role provides exposure to regulatory, compliance, and commercial legal issues, allowing a law student to gain hands on experience in a highly regulated environment. The Legal Intern will assist attorneys with research, drafting, and project-based work that contributes directly to the company’s mission of delivering quality and essential medicines.
Job Description
Responsibilities
- Conduct legal research on issues related to FDA regulations, state licensing, pharmaceutical marketing, manufacturing, privacy, and other healthcare compliance topics.
- Assist with drafting and reviewing contracts, policies, and other legal correspondence.
- Support the ongoing rollout of the Contract Pod AI (CPAI) platform, including learning system functionality and assisting with cross-functional integration efforts and user training.
- Help track and organize legal matters, including contract workflows and regulatory filings.
- Collaborate with cross-functional teams such as Regulatory Affairs, Quality, Government Affairs, and Commercial.
- Participate in meetings, prepare summaries, and contribute to special projects as assigned.
Minimum Requirements
- Must be currently enrolled in an accredited JD program with completion of at least one year of law school prior to the start of the internship.
- Demonstrated interest in healthcare or pharma.
- Strong legal research and writing skills, including ability to analyze laws and summarize findings.
- Excellent organizational skills with the ability to manage multiple tasks and deadlines.
- High attention to detail and accuracy, particularly in reviewing legal documents.
- Willingness to work in a hybrid environment, including reporting to the office at least two days per week to support collaboration, training, and engagement with management and internal stakeholders.
- Experience with MS Office (Word, Outlook, PowerPoint, Excel, Teams, etc.) and comfortable with learning new technology platforms.
- Motivated self-starter, operates independently, and possesses the ability to handle confidential information with discretion and sound judgment.
- Strong interpersonal and communication skills with the ability to interact with internal and external partners professionally.
Relationship with Others/Scope of Position
The Legal Intern will Interact with other team members and cross functionally on a regular basis.
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.
EEO Statement:
We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Endo Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Endo and has not been reviewed or approved by Endo.
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Fair & Transparent Compensation — Pay is considered competitive to good across many roles, with total compensation in commercial positions strengthened by sizable bonus/OTE when targets are met. Subsidiary experiences within the group also point to good compensation, reinforcing a generally positive pay story.
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Healthcare Strength — Core medical, dental, and vision coverage is strong, complemented by virtual care, disease‑management programs, and a health advocate service. Health coverage is described as good, adding perceived value beyond base pay.
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Retirement Support — A 401(k) plan provides a company match up to 4%, supporting employees’ long‑term savings. Current materials outline the matching formula clearly for prospective comparisons.
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What We Do
At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs. Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward. Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life. Endo has global headquarters in Malvern, Pennsylvania. Community Guidelines: 1. Be respectful. Everyone who visits our page should feel comfortable and respected. 2. If we see a comment that violates anything in the following list, it may be removed. • Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional. • Comments that are excessively repetitive and/or disruptive to the community. • Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter. • Comments that appear to be medical advice. We reserve the right to remove a reply for any reason at any time. 3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088. Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.








