Senior Quality Gxp Auditor

Verista Allentown , PA 18106

Posted 5 days ago

Looking for an exciting opportunity at a fast growing, employee-oriented company? Veristas 500+ experts team up with the worlds most recognizable brands in the life science industry to solve their business needs. Whether its compliance, quality management, verification, validation, automation, IT infrastructure, data analysis, manufacturing, or packaging, we deliver solutions that are right the first time.

Veristas experts include SMEs across the spectrum of pharma, medical devices and biotech industries. As a result, were uniquely capable of offering transformative, integrated solutions, new perspectives, and consistent results.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable our clients to improve the quality of patient healthcare worldwide. Our talented and dedicated professionals are committed to making an impact every day.

We deliver solutions that are right the first time.

Typical Responsibilities Include:

The Investigator is responsible to lead, conduct and document investigations relating to non-conformances and/or complaints within a GMP Pharmaceutical packaging organization. The Investigator will utilize root cause analysis tools, critical thinking and interviewing techniques to determine the root and contributing causal factors of non-conformances/complaints. The Investigator will offer recommendations to correct and/or prevent recurrence through CAPA design from the root cause conclusion of the investigation. The Investigator will lead, as necessary, the implementation of associated corrective and preventative actions through collaboration, teamwork and influence. The position will work closely and in collaboration with internal and occasionally external stakeholders. The Investigator also has responsibilities for data generation, process evaluation and performance metrics for the purposes of customer communication and driving continuous improvement


  • B.S./B.A. in scientific discipline as a minimum.
  • Minimum of +5 years of experience within Pharmaceutical / Biotech / Medical Device industry.
  • Demonstrated success in earning and maintaining a clients confidence through appropriate planning, organizing, controlling, and directing of a project.
  • Proven record of teamwork, problem solving, project tracking and facilitation of efficient communication between the client and the team.
  • Experience creating and working with high performance and high demand teams.
  • Quality orientation and high attention to detail.
  • Demonstrated ability to work with others and drive results.
  • Ability to think ahead and prepare sound action plans to achieve results.



Because employees are the key to our success, Verista offers strong benefits and incentives including:

  • Health, Dental, and Vision Insurance
  • 401(k) Retirement Plan with a company match
  • Paid Time Off Pay
  • Tuition Reimbursement
  • 9 Company Paid Holidays
  • Paid Long Term & Short Term Disability Insurance
  • Training and Development
  • Paid Maternity Leave and Parental Leave
  • Travel Bonus
  • Employee Referral Program
  • Tuition Reimbursement
  • Marriage Leave
  • Bereavement

*Verista is an Equal Opportunity Employer

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Senior Quality Gxp Auditor