Argenta

Director of Quality

Argenta  •  Shawnee, KS (Onsite)  •  1 hour ago
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Job Description

At Argenta, we’re more than a company — we’re a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it.

Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market.

We’re in a unique position. We are the world’s only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health.

Our uniqueness means:

We are ambitious, growing and building a ‘one team’ culture, guided by our values.

    • We are team players;
    • We are doers;
    • We are customer-centric;
    • We are innovators

We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best “paw” forward we will make the lives of the animals we care for, better.

With bases in New Zealand, the US, the UK and Europe, our 900+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Let’s Make It Happen, Together.

TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply.

Argenta is currently looking to fill the role of Director of Quality (Clinical) at our Shawnee, KSlocation. This position will overall all aspects of the clinical Quality department across the Americas CRO business.



Key Responsibilities:


  • Manage, lead and oversee all aspects of Quality department across Americas CRO embedding quality within operations and facilities using a risk-based, science-based approach
  • Develop and implement quality strategies that ensure scientific integrity, regulatory compliance, operational excellence and continuous improvement leading to controlled documentation and sustained inspection/audit readiness
  • Oversee QA and QC functions across business units within Americas CRO ensuring consistency and compliance
  • Build and lead a high performing team, embedding a culture of quality through coaching, training and cross-functional partnership
  • Manage and maintain quality systems and files across Americas CRO
  • Coordinate and perform internal audits and activities as requested
  • Perform qualification inspections/audits of selected vendors, laboratories, and clinical study sites
  • Conduct inspections/audits of company SOP programs and files (Qualification and Training files, SOP systems, Archiving, etc.)
  • Perform follow-up reviews of audit findings to confirm corrective actions have been completed
  • Provide oversight and participation in inspections by regulatory agencies and clients
  • Ensure the team has the skillset to support the following: drafting of QA and Data Management Plans, full capability to ensure drugs received for studies comply with regulatory, protocol and SOP compliance, auditing of protocols and Final Study Reports.

About You:

  • Bachelor’s degree, preferably in a scientific discipline or equivalent experience
  • Minimum of 10 years’ experience in a quality role in a highly regulated industry, including 4+ years of supervisory experience
  • Animal Health experience highly preferred
  • Demonstrated autonomy to lead a large, multi-functional quality department, drive enterprise-wide quality strategy, and partner with executive and operational stakeholders in a regulated environment
  • Progressive quality leadership experience in GCP and GLP compliant organizations
  • A collaborative working style to be able to lead and motivate people at all levels and across all functions in an organization
  • Experience conducting/acting as lead auditor for external audits
  • Experience conducting audits of study protocols in accordance with GCP guidance
  • Experience conducting study data audits
  • Experience auditing study reports (Final Study Reports (FSRs)
  • Experience conducting internal inspections/audits.
  • Experience working with EDC systems (Electronic Data Capture)
  • Position requires significant computer skills including the ability to use Microsoft Word, Excel, PowerPoint, and Adobe Acrobat
  • The employee must possess a valid driver’s license and proper travel documentation i.e., passport, and have the ability to travel
  • Excellent oral and written communication skills
  • Strong analytical thinking and problem-solving skills
  • Capable of working in a changing environment and under pressure
  • Supports organizational goals and objectives aligned to strategic and/or operations plans

Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued. At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through a strong culture, great benefits, and growth opportunities.

Argenta is an equal-opportunity employer

To find out more about Argenta, click here: www.argentaglobal.com

Argenta

About Argenta

At Argenta, we’ve been collaborating with clients worldwide since 2006, bringing expertise, innovation, and a can-do attitude to deliver cutting-edge animal health & nutrition, and human nutrition solutions.

Why Argenta?

We are the only global CRO and CDMO focused exclusively on animal health & nutrition, complemented by regulatory expertise in human nutrition. We provide tailored, end-to-end solutions from Molecule to Market at any scale.

Our Three Pillars:

• Global Partnerships – turning ideas into reality worldwide

• Molecule to Market Approach – guiding products from research to launch

• Innovation – driving progress in animal & nutrition, and human nutrition

Our Services:

• R&D: innovative animal health & nutrition solutions, fully EMA/FDA/EFSA compliant

• Pre-Clinical Research: dedicated teams in Spain, Germany, and the US providing confident go/no-go decisions

• Clinical Research: agile, high-quality veterinary studies delivered on time and within budget

• GMP Manufacturing: facilities in New Zealand, the US, and the UK

• Regulatory & Scientific Consultancy: expert support for medicinal products, feed additives, and human nutrition products (novel foods, food additives, enzymes, etc)

• Full Product Development: from concept to market

Collaboration at Our Core:

950+ experts in science, veterinary, engineering, and regulatory affairs, working closely with clients to develop products that truly make an impact.

Our Story:

Founded in New Zealand by scientist Doug Cleverly, Argenta combines Kiwi ingenuity with global collaboration. Our roots as a trusted CRO go back to 1987, built on scientific excellence and long-term partnerships.

Today, through our CMO & CDMO facilities, we optimize efficacy trials, accelerate product development, and help companies turn innovative ideas into market-ready products.

We also support human nutrition projects, guiding companies through regulatory pathways to successfully launch new products.

Let’s make it happen - together!

Industry
Chemicals & Materials
Company Size
501-1,000 employees
Headquarters
Auckland, NZ
Year Founded
2006
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