Intern, Operational Excellence / Operations

Reposted 5 Days Ago
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Rochester, MI
In-Office
1-1 Annually
Internship
Healthtech • Pharmaceutical • Telehealth
The Role
The internship involves supporting initiatives in Manufacturing Operations, Quality, and Engineering, focusing on CAPA execution, continuous improvement, and engineering troubleshooting, while applying educational knowledge in a corporate setting.
Summary Generated by Built In

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
Position summary
Support critical initiatives across Manufacturing Operations, Quality, and Engineering with focus on CAPA execution, continuous improvement, investigation support, engineering troubleshooting, and AI use-case development. Maintain accurate execution, produce clear documentation, and deliver measurable project outcomes in a regulated environment.

Job Description

Key responsibilities

  • Maintain CAPA execution; drive action updates, due-date adherence, and closure evidence packages
  • Prepare CAPA meeting materials, minutes, and follow-up action lists
  • Support deviation/nonconformance investigations through fact gathering, evidence organization, timelines, and root-cause tool documentation (5-Why, fishbone)
  • Develop investigation and CAPA documentation templates/checklists to improve completeness and cycle time
  • Support continuous improvement initiatives including 5S, visual management, standard work, process mapping, and Kaizen activities
  • Collect and analyze baseline performance data (time studies, downtime, defects, rework); summarize findings and trends
  • Build basic dashboards and visual boards in Excel/PowerPoint/SharePoint and maintain version control
  • Support on-floor engineering troubleshooting by documenting symptoms, conditions, actions taken, and outcomes; convert learnings into standard work updates
  • Identify and document AI “base-case” opportunities for repetitive work reduction; define problem statements, inputs/outputs, benefits, risks, controls, and adoption steps
  • Produce project summaries and deliverables for cross-functional leadership reviews

Qualifications

  • Currently pursuing a Bachelor’s degree in Engineering, Operations, Supply Chain, Quality, Data/Analytics, or related field
  • Proficiency in Excel and PowerPoint; strong documentation and organizational skills
  • Ability to work in a regulated environment with strict adherence to safety, quality, and procedural requirements
  • Strong written and verbal communication; ability to collaborate across Operations, Quality, and Engineering

Preferred qualifications

  • Basic knowledge of Lean/CI tools (5S, standard work, Kaizen, root cause analysis)
  • Experience with data visualization or automation (Power Query, macros, Python)
  • Basic familiarity with quality systems (CAPA, deviations, investigations)

Deliverables

  • Continuous improvement projects with baseline, implementation, and sustainment documentation
  • AI use-case inventory with business cases, effort estimates, and risk/control considerations
  • Investigation support packages with timelines and organized evidence
  • Current CAPA and action-item tracker with weekly status reporting.

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. 

Top Skills

Excel
Power Query
PowerPoint
Python
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The Company
Montreal, Quebec
1,722 Employees
Year Founded: 1997

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.

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