Quality Assurance Auditor Crop Protection

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 you're ready to be part of a team that values these principles, we want to hear from you!

Think Globally. Act Locally.

OVERVIEW

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.

YOUR ROLE

• 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

YOUR PROFILE

• 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

WHAT WE OFFER

• 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 application@knoell.com. If you're 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!