Senior Regulatory Affairs Manager
Boost your chances before you apply.
Argenta
Shawnee, KS, US
Summary
Facilitates regulatory and drug development requirements for external clients and internal projects within the animal health sector. Provides expert regulatory advice and represents the company in industry associations to identify new consulting opportunities.
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 organisation (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 650+ 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 Senior Regulatory Affairs Manager within our CRO Americas division.
About the role:
- Facilitates and supports the regulatory and drug development requirements of external clients and internal projects
- Effectively manage client and stakeholder expectations by providing timely, relevant, and accurate documents, assessments, reports and communications
- Demonstrates an awareness of current regulations, guidance's, regulatory processes, and the animal drug development process, while maintaining a flexible and creative mindset to work through regulatory challenges
- Creates regulatory solutions to complex issues
- Provides client accurate expert regulatory advice on animal health product development
- Represent Argenta in industry associations (e.g. GADA, AHI, SQA)
- Identify and pursue new regulatory consulting opportunities which may include meeting with new clients, traveling and speaking at professional meetings, networking in the industry and contributing to various publications
Requirements:
- Bachelor’s degree or equivalent experience in a scientific discipline, advanced degree (DVM, PhD, MS) is preferred
- 8+ years experience in veterinary regulatory and/or animal drug development
- Proven experience includes several of the following: CVM, E-Submitter, GLP, GCP, GMP, USDA, EPA, EMA
- Development and regulatory experience with food animal drugs is preferred but not required
- Good written and oral communication skills, and ability to work collaboratively within and across teams
- Results and bottom line oriented
- Excellent analytical skills and attention to detail
- Proven influence, negotiation and persuasion skills
- Defines and plans priorities well. Comfortable balancing shifting priorities as required to meet business needs
This position is subject to a DEA background check post offer and at regular intervals. This position is also required to complete a post offer drug test. Both the background and drug test must comply with company standards or offers of employment will be rescinded.
You will also be someone who is aligned with our company values of "We are Doers, We are Team Players, We are Innovators, We are Customer-Centric".
We pride ourselves on the uniqueness of our development and manufacturing abilities and the skills and qualities of our team.
The position is a remote position working out of your home with domestic and occasionally international travel. Due to the nature of being a global organization, there may be times when this role works outside of normal business hours. Those times would be provided to the employee with plenty of notice.
Want to know more about Argenta? Visit our website www.argentaglobal.com
Equal Opportunity Employer
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!
Founded
2006
Company size
501-1,000 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Auckland, New Zealand
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!
Founded
2006
Company size
501-1,000 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Auckland, New Zealand