Are you an experienced Development Chemist with strong expertise in analytical method development, troubleshooting and product characterisation, including NCEs? Do you want to be part of a truly unique company that makes a meaningful impact on the well-being of animals? If so, we have an exciting opportunity for you!
- Full time permanent role
- Global researcher & manufacturer of animal health pharmaceuticals
- South Auckland location with onsite parking
We are in the animal health business, partnering with our clients in the areas of Research and Development (R&D) and manufacturing to produce pharmaceuticals for both farm and companion animals. Originally founded in 2006 by a New Zealand chemist with an entrepreneurial mindset, Argenta’s vision is “Healthier Animals, Sustainably”. Our recipe for success has been our uniqueness in our vision and our people. Argenta now has operations across 6 sites with locations in New Zealand, the United States, Scotland, Spain, and Germany with over 900 employees globally.
About the role:
Reporting directly to the Method Development Supervisor, you will lead the development and optimisation of analytical methods for drug substances and products, troubleshoot complex technical challenges, and provide scientific expertise to drive product development and method validation excellence.
The working hours for this role is Monday to Friday, 8:00pm to 5:00pm finish. The key focus areas are to provide scientific leadership in analytical method development and troubleshooting to deliver robust, compliant product development outcomes at Argenta.
You will be required to comply with pharmaceutical good manufacturing practices (GMP), principles and protocols and follow the standard operating procedures (SOPs), and quality standards in a safe and timely manner.
About you:
We are looking for someone who is an experienced analytical chemist with expertise in method development, validation and troubleshooting across pharmaceutical or product development environments. Strong problem-solver with a scientific mindset, capable of delivering robust analytical solutions and technical leadership in complex R&D settings.
Naturally energetic and driven, you will have a keen focus on quality and attention to detail, essential in meeting the stringent pharmaceutical regulations we adhere to.
Your background, experience and attributes will include:
- Previous experience in the Pharmaceutical Industry in Analytical Method Development [minimum 15 yrs experience].
- Experience in a GMP / GLP compliant environment.
- Expert in using and troubleshooting key Analytical Instruments and software.
- Knowledge of the pharmaceutical regulatory approval processes and requirements for submission of Drug Substance and Drug Product.
- Providing technical expertise and direction to a team of Chemists.
- Strong understanding of health and safety requirements.
- The ability to manage resources to meet changing priorities.
- Strong computer literacy with the ability to pick up new packages and processes easily.
- Strong numeracy skills and the ability to analyse and interpret data.
- Excellent written and verbal English language communication skills
Why Join Us?
This is an opportunity to join a unique and fast-growing business where your ideas matter, your skills will grow, and your contribution is genuinely valued. Along with a competitive salary, you’ll enjoy comprehensive insurance cover, access to EAP support, fresh fruit every week, and regular on-site events that bring people together.
You will also be part of a workplace that truly values its people and encourages collaboration, fresh thinking, and doing great work together. If you are an experienced professional looking for a challenging and rewarding opportunity, we want to hear from you!
To apply, please submit your CV and a cover letter outlining your experience and motivation for the role.
Are you an experienced Development Chemist with strong expertise in analytical method development, troubleshooting and product characterisation, including NCEs? Do you want to be part of a truly unique company that makes a meaningful impact on the well-being of animals? If so, we have an exciting opportunity for you!
- Full time permanent role
- Global researcher & manufacturer of animal health pharmaceuticals
- South Auckland location with onsite parking
We are in the animal health business, partnering with our clients in the areas of Research and Development (R&D) and manufacturing to produce pharmaceuticals for both farm and companion animals. Originally founded in 2006 by a New Zealand chemist with an entrepreneurial mindset, Argenta’s vision is “Healthier Animals, Sustainably”. Our recipe for success has been our uniqueness in our vision and our people. Argenta now has operations across 6 sites with locations in New Zealand, the United States, Scotland, Spain, and Germany with over 900 employees globally.
About the role:
Reporting directly to the Method Development Supervisor, you will lead the development and optimisation of analytical methods for drug substances and products, troubleshoot complex technical challenges, and provide scientific expertise to drive product development and method validation excellence.
The working hours for this role is Monday to Friday, 8:00pm to 5:00pm finish. The key focus areas are to provide scientific leadership in analytical method development and troubleshooting to deliver robust, compliant product development outcomes at Argenta.
You will be required to comply with pharmaceutical good manufacturing practices (GMP), principles and protocols and follow the standard operating procedures (SOPs), and quality standards in a safe and timely manner.
About you:
We are looking for someone who is an experienced analytical chemist with expertise in method development, validation and troubleshooting across pharmaceutical or product development environments. Strong problem-solver with a scientific mindset, capable of delivering robust analytical solutions and technical leadership in complex R&D settings.
Naturally energetic and driven, you will have a keen focus on quality and attention to detail, essential in meeting the stringent pharmaceutical regulations we adhere to.
Your background, experience and attributes will include:
- Previous experience in the Pharmaceutical Industry in Analytical Method Development [minimum 15 yrs experience].
- Experience in a GMP / GLP compliant environment.
- Expert in using and troubleshooting key Analytical Instruments and software.
- Knowledge of the pharmaceutical regulatory approval processes and requirements for submission of Drug Substance and Drug Product.
- Providing technical expertise and direction to a team of Chemists.
- Strong understanding of health and safety requirements.
- The ability to manage resources to meet changing priorities.
- Strong computer literacy with the ability to pick up new packages and processes easily.
- Strong numeracy skills and the ability to analyse and interpret data.
- Excellent written and verbal English language communication skills
Why Join Us?
This is an opportunity to join a unique and fast-growing business where your ideas matter, your skills will grow, and your contribution is genuinely valued. Along with a competitive salary, you’ll enjoy comprehensive insurance cover, access to EAP support, fresh fruit every week, and regular on-site events that bring people together.
You will also be part of a workplace that truly values its people and encourages collaboration, fresh thinking, and doing great work together. If you are an experienced professional looking for a challenging and rewarding opportunity, we want to hear from you!
To apply, please submit your CV and a cover letter outlining your experience and motivation for the role.