Senior Auditor Enterprise Quality Auditing

Posted 4 Days Ago
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Hiring Remotely in Woodcliff Lake, NJ
Remote
Senior level
Healthtech • Pharmaceutical • Telehealth
The Role
The Senior Auditor will organize and perform quality audits for suppliers, third parties, and internal sites ensuring compliance with industry quality standards. Responsibilities include conducting audits, preparing reports, tracking audit responses, and supporting continuous improvement initiatives. The role also involves participating in preparation for regulatory inspections and providing cGMP guidance.
Summary Generated by Built In

Why Endo?

We want the best and brightest people at Endo to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life.
At Endo, we are building a diverse, equitable and inclusive workplace, and we are looking for talented individuals to join our team.

Job Description Summary

Independently organizes and performs quality audits under general direction. The audits include suppliers/vendors, third parties, Endo’s business units and internal manufacturing sites that support marketed drug products to ensure products, controls, policies and processes meet Pharmaceutical/Biotechnology industry quality standards. Participates in Pre-Approval Mock Inspections to prepare internal & CMO facilities for regulatory inspections and assesses gaps in the quality systems and overall infrastructure. Provides cGMP guidance for continuous improvement projects to ensure compliance with regulations and current industry standards. Assists in the evaluation of metrics to determine trends and opportunities for continuous improvements. Provides support during regulatory agency and external third party inspections. Possess sound technical knowledge and auditing experience in multiple areas, such as API, Analytical Laboratories, Sterile Drug Product, Contract Packaging, Mock PAI, etc.

Job Description

Key Accountabilities - key outcomes/deliverables, the major responsibilities, and % of time

Responsibilities

85% of Time:

  • Supports the audit program by independently conducting internal and external audits or participating as an audit team member
  • Contributes to the development of the annual audit plans and schedules
  • Schedules audit activities and provides audit agenda
  • Prepares audit reports and communicates findings to external and internal stakeholders
  • Tracks audit responses and auditee’s CAPAs through completion and closeout
  • Expand technical knowledge and auditing experience as lead auditor across the range of branded product suppliers (i.e. API, Sterile Drug Product, Mock PAI, etc.)
  • Support collection and collating of applicable key auditing performance parameters in contribution of reporting metrics

15% of Time:

As related to Enterprise Quality Auditing Functions:

  • Provides guidance for continuous improvement to ensure compliance with regulations and current industry standards
  • Assists in the evaluation of metrics to determine trends and opportunities for continuous improvements
  • Participates in the development and implementation of EQA programs, policies, procedures, agreements & controls
  • Participates in periodic audit review meetings
  • Supports regulatory agency and external third party audits
  • Participates in Mock PAIs of internal sites & CMOs to prepare for audits and assess gaps in the system

Commitment to Diversity, Equity, and Inclusion:  

At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person’s unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.

EEO Statement:

At Endo, we firmly believe in the principles of equal employment opportunity and strive to create an atmosphere where all employees, regardless of their race, color, creed, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability (including pregnancy), age, or military or veteran status, feel valued, respected, and empowered. Our commitment to EEO extends to every aspect of employment, including recruitment, hiring, training, promotions, compensation, benefits, transfers, terminations, and all other employment practices. We are dedicated to ensuring that all employment decisions are based on qualifications, skills, and merit.

The Company
Montreal, Quebec
1,722 Employees
On-site Workplace
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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