Quality Assurance Auditor Crop Protection

Knoell

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profile Job Location:

Durham, NC - USA

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Join Us in Shaping the Future of Regulatory Services.

knoell is one of the leading global service providers in regulatory registration clinical development and product development support. As a family-owned business we take pride in our commitment to the highest standards and believe that people are at the heart of our success. With our team of scientific and regulatory experts and an extensive network of partners we ensure reliable solutions that address our clients global business needs right from the start.

At knoell we are guided by our core values of commitment reliability excellence and diversity. Are you someone who thrives in a collaborative environment Do you take pride in delivering high-quality results and upholding excellence in everything you do At knoell we are passionate about embracing diverse perspectives knowing that this fuels innovation and strengthens our impact. If youre ready to be part of a team that values these principles we want to hear from you!

Think Globally. Act Locally.

The Quality Assurance Auditor is responsible for auditing facilities and studies to ensure compliance with Good Laboratory Practice (GLP) standards and related documentation for regulatory submissions.

This role involves inspecting and reviewing testing facilities study protocols study conduct raw data and draft study reports in alignment with GLP principles and applicable test guidelines. The Quality Assurance Auditor prepares inspection reports and verifies at finalization that all findings have been appropriately addressed. Upon completion the Auditor issues and signs a Quality Assurance Statement.

The position requires strong expertise in agricultural practices analytical chemistry and comprehensive knowledge of Good Laboratory Practice (GLP) regulations.

  • Inspect testing facilities to ensure frameworks are in place for studies to meet GLP requirements
  • Audit studies supporting the authorization of crop protection products including:
    • Reviewing draft protocols for GLP compliance and alignment with test guidelines
    • Inspecting raw data for accuracy and integrity
    • Observing the in-life phase of studies during conduct
    • Reviewing draft study reports for accuracy completeness and compliance
    • Preparing inspection reports and verifying corrective actions have been addressed
  • Work independently and audit complex studies
  • Act as a key contact for clients offering solutions to study-related challenges
  • Coach and review the work of less experienced QA staff
  • Collaborate with clients regulatory bodies and internal teams to ensure reporting accuracy and compliance
  • Advise staff on GLP policies and best practices
  • Maintain records and documentation supporting Quality Assurance activities
  • Approach tasks flexibly adapting to new and varied challenges
  • Undergraduate degree (or equivalent experience) in agriculture analytical chemistry biology food chemistry or a related discipline
  • Minimum of 2 years of relevant professional experience
  • Strong knowledge of agricultural practices and analytical chemistry
  • Excellent English skills (spoken and written); additional languages are an asset
  • Strong communication skills both verbal and written
  • Exceptional attention to detail organizational ability and prioritization skills
  • Ability to engage with clients mindfully and effectively identifying additional client needs
  • Experience working in multicultural teams within a global environment
  • Commitment to delivering an outstanding customer experience in client project
  • Work in a dynamic family-owned business environment with an international team where new ideas creative approaches and collaboration are valued. You will have the opportunity to work with market leaders in our industry.
  • Development is at the core of our culture. At knoell we offer opportunities to support your personal leadership and technical growth including English language courses to help you communicate effectively in our business language.
  • We value work-life balance and support part-time arrangements where business requirements allow.
  • At knoell you can participate in our global employee referral program and get rewarded for referring talent to the company.
  • For our U.S.-based colleagues knoell offers a competitive compensation and benefits package including medical dental vision life and disability insurance 401(k) with company match and tuition reimbursement.
  • We are an Equal Opportunity Employer and do not discriminate based on race color religion age sex national origin disability status genetics protected veteran status sexual orientation gender identity or expression or any other characteristic protected by federal state or local laws.
  • knoell is a drug-free workplace. New hires may be required to pass a pre-employment drug test.
  • knoell complies with federal and state disability laws and makes reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed during the application or interview process please contact our Global Recruiting department.
  • The above description is intended to reflect the general nature and level of work performed. It is not a comprehensive list of all duties responsibilities qualifications or working conditions and management reserves the right to revise it at any time.

If you have any questions feel free to reach out to us at. If youre looking to join a global leader in regulatory and clinical services where you can make a real impact and contribute to a team that values your contributions then knoell is the place for you.

We look forward to receiving your application!


Required Experience:

Unclear Seniority

Join Us in Shaping the Future of Regulatory Services.knoell is one of the leading global service providers in regulatory registration clinical development and product development support. As a family-owned business we take pride in our commitment to the highest standards and believe that people are ...
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Key Skills

  • Laboratory Experience
  • Quality Assurance
  • FDA Regulations
  • ISO 9001
  • Quality Audits
  • Quality Management
  • GLP
  • cGMP
  • EPA
  • QA/QC
  • Toxicology Experience
  • Aviation Experience