Our company is our people. We, at Argenta, continually provide innovative turnkey services for our clients from pre-formulation to global supply - specializing in animal health.

If you are a talented and committed professional in the areas of:

  • Formulation / analytical development
  • Clinical Research
  • Commercialisation
  • Manufacturing/Production & Packaging
  • Quality Control
  • Quality Assurance
  • Regulatory Support
  • Logistics / Supply chain
  • Project Management

We invite you to explore dynamic career opportunities with an exciting and ever growing organization. Write to us at jobs@argentaglobal.com

Our Values

Our Values

Positions Available

Senior Production Engineer

15/06/2017

Argenta is a New Zealand owned company that undertakes contract R&D and manufacturing for global and local organisations specialising in animal health products. We have state of the art manufacturing facilities located in Manurewa with a manufacturing and R&D footprint throughout USA and Europe.

We're on the look out for an experienced Senior Production Engineer. The key purpose of this role is taking responsibility for process improvement, technical trouble shooting and manufacturing investigations, process scale up and process validation. Reporting to the Technical Manager, you will ensure the successful technical transfer of products into commercial production while ensuring GMP compliance is adhered to at all times. You will be a skilled Chemical Engineer with experience managing multiple projects and with strong technical intellect, coupled with excellent relationship, communication and reporting skills.

You will be someone who has the academic understanding and ability, but also likes to be hands-on and enjoys the challenge of identifying issues, conducting the investigation and then advising and implementing best practice. By nature you'll be an energetic, driven person with a focus on quality and detail being imperative as we are regulated by the strictest of pharmaceutical standards.

This is a permanent full time role and the hours of work are 7.30am to 4.00pm Monday to Friday with some overtime and weekends required as production schedules and demands require.

Your key responsibilities will include:

  • Providing technical support to production
  • Continuously improving all aspects of production operations including automation
  • Preparing validation documentation (protocol and reports)
  • Updating and maintaining SOP’s for equipment and processes
  • Dealing with manufacturing investigations including preparing corrective and preventative action reports
  • Reporting on manufacturing and quality measures including trend analysis
  • Perform risk assessments and make sound technical decisions based on data
  • Ensuring Technical Transfer of products into commercial production meets GMP standards
  • Maintaining Health & Safety processes and compliance and identifying new technologies

Your background, experience and attributes will include:

  • A tertiary qualification in Operations, Chemical Engineering or similar
  • Knowledge of GMP and FDA/EU manufacturing and validation regulations
  • A minimum of 5 years manufacturing experience preferably in a Pharmaceutical environment
  • Skilled in examining, developing and implementing new strategies and procedures
  • Well-developed report writing and editing skills including the use of relevant MS Office software
  • Excellent relationship management and communication skills [written and verbal]

If this sounds like the opportunity you've been waiting for, please take the time to put together a cover letter which reflects who you are and why you want this role, attach your CV and email recruitment@argenta.co.nz

Project Engineer

15/06/2017

Argenta is a New Zealand owned company that undertakes contract R&D and manufacturing for global and local organisations specialising in animal health products. We have state of the art manufacturing facilities located in Manurewa with a manufacturing and R&D footprint throughout USA and Europe.

The key purpose of this role is taking responsibility for process improvement of plant and equipment such as instrumentation and control systems. Reporting to the Engineering Manager, you will support production by focusing on technical trouble-shooting, supporting manufacturing investigations, scoping new plant and equipment requirements and project managing installations. We are looking for a skilled Engineer with a strong technical intellect, familiar with solid dose & liquid handling/processing equipment and an understanding of automation & control, coupled with excellent relationship, communication and reporting skills

You will be the sort of person who has academic understanding and ability, but also likes to be hands-on and enjoys the challenge of identifying issues, conducting the investigation and then advising and implementing best practice. By nature you'll be an energetic, driven person with a focus on quality and detail being imperative as we are regulated by the strictest of pharmaceutical standards.

This is a permanent full time role and the hours of work are typically 7.30am to 4pm Monday to Friday with some overtime and weekends required as production schedules and demands require.

Your key responsibilities will include:

  • Scoping new plant and equipment to meet business needs such as process and quality improvement and GMP compliance
  • Oversight and project management of CAPEX production projects eg. plant, equipment and instrumentation installations, and facility improvements/site expansion
  • Ensuring Technical Transfer of products into commercial production meets GMP standards
  • Ensuring routine plant and equipment calibrations are performed on schedule
  • Maintaining Health & Safety processes and compliance and identifying new technologies

Your background, experience and attributes will include:

  • A tertiary Engineering qualification eg. BE, Mechatronics/Mechanical
  • Proven experience in quality focused manufacturing environment including technical projects eg. equipment installations, plant set-up
  • Previous experience and knowledge in a GMP or highly regulated product environment preferred
  • Well-developed report writing and editing skills including the use of relevant MS Office software
  • Excellent relationship management and communication skills [written and verbal]

If the sound of this opportunity excites you, please put together a cover letter which reflects who you are and why this role is of interest to you, attach your CV and apply to recruitment@argenta.co.nz

Head of Pharmaceutical Sciences

19/09/2017

As a result of local and international expansion, we have an opportunity in our Research and Development department for a Head of Pharmaceutical Sciences in Auckland, New Zealand. The focus of this role is to lead our NZ Pharmaceutical Sciences team of 7 direct and 50+ indirect reports including product development, analytical sciences, and method creation as well as compliance and Laboratory Services teams.

As a member of the Argenta New Zealand Leadership Team and Global Pharmaceutical Sciences Management Team, this is a key position within Argenta R&D where you will be responsible for the on-going development of R&D projects from initiation to completion while implementing departmental efficiencies, developing and implementing strategic growth plans to meet financial targets, and providing a high level of scientific guidance to all team members.

Your key responsibilities will include:

  • Leadership and on-going strategic development of the NZ Pharmaceutical sciences department
  • Staff motivation, retention, training, and recruitment
  • Support business development activities by providing technical documents, expertise and preparing new client proposals
  • Manage a departmental budget and prepare and present monthly financial updates and reports to the board
  • Work with PMO to schedule resource in accordance with company priority
  • Lead regular departmental meetings
  • Drive Argenta Health, Safety and Environment culture and compliance within the team

Your background, experience and attributes will include:

  • A tertiary degree in relevant scientific discipline
  • Experience within the pharmaceutical industry to a minimum of 15 years
  • Personnel, project and fiscal management experience
  • Knowledge of the pharmaceutical regulatory and product approval processes
  • Excellent interpersonal, written and verbal communication skills

Argenta has strongly embedded company values which is key to who we are and how we deliver, whether it's internal or external relationships. By nature, you’ll be an energetic, driven person who shares the same values as us.

On offer is an opportunity to join a successful and rapidly expanding business where your abilities will be valued along with a competitive remuneration package and an exciting and challenging role.

If this sounds like the opportunity you’ve been waiting for, please take the time to put together a cover letter explaining why the position and company is of interest and what you would bring to the role, attach your CV and email it to recruitment@argenta.co.nz.

Formulation and Development Team Leader

19/09/2017

Lead a small team on exciting pharmaceutical R&D formulation and product development projects where you will be working directly with world leading pharmaceutical research companies.

Due to continued growth and lots of exciting projects coming on stream, we are looking for a team leader for our pharmaceutical sciences formulation and development team. This team conducts contract pharmaceutical development projects that range from pre-formulation activities through to manufacture of clinical trial material and all regulatory studies leading to registration and commercial supply. Having an international client base and exporting to over 60 countries, Argenta is unique in terms of the incredible variety of R&D projects we undertake, so this role is sure to keep the right person busy and challenged.

Your background could be from a small or global pharmaceutical company where you have been involved from conception to completion of the product development lifecycle, including overcoming all the obstacles along the way. You will be familiar with working in a cGMP environment and from your previous roles you will most likely have developed a number of products in various dosage forms.

You will be dealing with multi-national pharmaceutical companies located all over the world, therefore building and maintaining “virtual” relationships is absolutely vital, as is being able to prepare high quality technical documents. By nature, you’ll be an energetic, driven person with a desire to continually improve systems, processes and the overall customer experience.

This role is a leadership position where your time will be split between mentoring and managing a small team while also conducting hands on formulation development activities.

Your key responsibilities will include:

  • Lead a team of formulation and development scientists and technicians
  • Providing technical expertise and direction to the formulation and development team
  • Work with Formulation & Development Manager to conduct studies and generate data required to develop new products
  • Manage product development projects from proof of concept pre-formulation to clinical and pivotal stability supply
  • Provide regular staff and project updates to manager

Your background, experience and attributes will include:

  • A relevant tertiary qualification in science discipline, preferably Pharmacy/Pharmaceutical Sciences or Chemistry
  • Solid dose and liquid formulation development experience required
  • A minimum of 8 years’ experience in the pharmaceutical industry or related field
  • A thorough understanding of the regulatory requirements involved in drug development
  • Excellent report writing skills • Experience in project leadership and people management
  • Strong relationship management and communication skills [written and verbal]

If this sounds like the opportunity you’ve been waiting for, please take the time to put together a cover letter which reflects who you are and why you want this position, attach your CV and send to recruitment@argenta.co.nz

Associate Chemist or Chemist

30/10/2017

AML Riverside in Fort Dodge, Iowa is expanding our analytical services group and are seeking experienced Chemists or Associate Chemists to join the team.

Depending on your experience, responsibilities include (but not limited to) performing sampling and testing of packaging components, raw materials, utilities, and products in compliance with site systems/procedures and cGMPs including:

  • Write analytical test methods and procedures
  • Review USP/NF, forum, and supplements for applicable changes impacting testing
  • Perform sampling and testing of packaging components, raw materials, in-process samples, finished products and stability samples.
  • Perform testing using HPLC, GC, and FT-IR
  • Validation of laboratory instruments
  • Validation and transfer of methods
  • Review and sign-off analytical data and documentation
  • Qualification, calibration and maintenance of laboratory equipment
  • Perform out-of-specification/out-of-trend investigations to determine root cause and implementation of CAPAs

Qualifications/Experience:

  • Requires a science degree relevant to the pharmaceutical industry and a minimum of 5 years of laboratory experience in a GMP regulated industry.
  • Possess a strong understanding of cGMPs and FDA regulations.
  • Requires excellent written and communication skills as well as attention to detail.
  • Able to perform testing, maintenance, and troubleshooting on laboratory instruments to include HPLC, GC, and FT-IR.
  • Validation and method transfer experience preferred. Functional knowledge of Microsoft Office products. Full- or flex-time positions available!

To apply, please send resume to people@amlriverside.com.

Analytical Development Scientist

06/11/0201

Are you an enthusiastic and motivated scientist that would enjoy working on a variety of development projects? This is a great opportunity to make a lasting contribution in a NZ owned and operated business, working with the world’s leading pharmaceutical research companies.

Due to continued growth, we are looking to add a full-time scientist to our R&D team based in Lawrence, Kansas. This team conducts contract development projects that include chemical analysis, formulation development, technical transfers and commercial support.

Your key responsibilities will include:

  •  developing and validating new analytical methods
  • performing routine analytical testing and providing technical support for R&D projects
  • generating, documenting and communicating technical data
  • assisting with formulation development as required

We are looking for a candidate who has:

  • a BS degree in a science discipline, preferably Chemistry or Pharmaceutics
  • at least 1-2 years previous experience in analytical development in the pharmaceutical industry
  • previous experience within a GMP/GLP compliant environment
  • analytical instrumentation and software skills e.g. HPLC, GC, Chromeleon
  • excellent verbal and written communication skills and a high level of computer literacy

This role will be challenging and rewarding, where your full technical skills can be utilised, and the ability to think outside the box whilst ensuring targets are met will be hugely beneficial. This is an exciting opportunity to join a global R&D team that expects to deliver world class science.

If you meet the above criteria and are interested in this opportunity, please send a cover letter/email and resume to joanna.pratt@argentaglobal.com.

Group Finance Manager

07/11/2017

Argenta is growing and we’re on the lookout for global talent to join us on our journey.

Founded in 2006 with approximately 70 staff now sitting at over 400, Argenta is a New Zealand-owned company that creates, develops and manufactures products for the global animal health industry. With operations in New Zealand, the United States and Scotland, we provide contract R&D and manufacturing services to our global clients, as well as inventing new products and drug delivery technologies.

Due to significant growth in the past few years, we are now recruiting a newly created Group Finance Manager position. Reporting to the CFO, this role is tasked with management and board reporting, consolidations and statutory accounting.

We pride ourselves on a great company culture built around a strong set of values, and we look for a good balance of technical skill and shared vision in our people. This means you’ll be highly competent at what you do (the best in your field!), but also passionate about our company values, which are key to who we are and how we work. We actively develop our people and there are career opportunities available for the right candidate.

Through your previous experience you will be someone who has the ability to see complex projects through from beginning to end and be able to identify, prioritise and manage all the steps in between. A focus on quality, accuracy and details is imperative as we are regulated by the strictest of standards.

Your key responsibilities will include:

  • Supporting the on-going development and execution of the Group Finance strategy and business priorities
  • Educating, influencing and leading direct reports/key internal stakeholders on financial compliance and statutory requirements
  • Driving continuous improvement of the groups finance systems and processes to ensure they meet the needs of the business, clients and legislative requirements
  • Monthly management and board reporting
  • Consolidation of monthly accounts across NZ, US, UK
  • Statutory accounting
  • Overseeing the audit processes
  • Global tax, including transfer pricing
  • Treasury functions including cashflow management
  • Managing external relationships including auditors, banks and insurers

Your key to success:

  • CA (or similar) qualification
  • 6+ years’ post qualification experience
  • Have a strong customer service focus matched by a ‘hands on, can-do attitude’
  • Have initiative and be a self-starter, with the ability to lead a right first time culture
  • Good analysis and problem solving skills
  • Excellent verbal communication and the ability to engage and gain buy-in at all levels
  • Sound written communication and report writing skills
  • A collaborative leadership approach which brings people on the journey

By nature, you’ll be a hands on, lead by example leader, energetic, driven person with a desire to continually improve systems, processes and the overall customer experience. Continuous improvement will be your passion; you will embrace change: continuously thinking about how to do something better, faster and adding more value. You will see finance as a service that enables Argenta to meet its ambitious growth plans.

Does this sound like you? Send us a brief cover letter that reflects who you are and why you want this position, attach your CV, and email it to tasi.pocock@argenta.co.nz

Recruitment Advisor

10/01/2018

Argenta is growing and we’re on the lookout for an experienced recruiter to join us on our journey by supporting the business in sourcing and attracting like-minded people that have a good mix of technical capability, culture fit and shared vision and purpose.

Founded in 2006 with approx. 70 staff now sitting at over 400, Argenta is a New Zealand-owned company that creates, develops and manufactures products for the global animal health industry. With operations in New Zealand, the United States and Scotland, we provide contract R&D and manufacturing services to our global clients, as well as inventing new products and drug delivery technologies.

Through your previous experience you will be someone who has the ability to see the full recruitment cycle through from beginning to end and be able to identify, prioritise and manage all the steps in between. This is not your run of the mill recruiter role, as you’ll be working with our HR Business Partner to develop talent sourcing strategies and deliver training to our people leaders.

Your authentic and credible approach will see you immerse yourself in the business of our diverse, values driven people leaders where you will be respected for your ability to constructive challenge, lift leadership capability and demonstrate a breadth of vision and perspective. They will rely on you to understand their big picture, and see opportunities to add value. Diverse is the perfect word to describe Argenta with a unique mix that includes Manufacturing, Quality, R&D and Shared Services.

Being successful means you will demonstrate agility and responsiveness and quick to think on your feet to deliver excellence across multiple and conflicting priorities with ease. You'll be an experienced recruiter who has developed talent sourcing and acquisition processes, articulate, confident and knows the importance of working alongside leaders to provide credible solutions and providing insightful advice, with a collaborative engaging approach.

A snapshot of what you’ll be doing

  • Provide best practice talent sourcing and acquisition solutions to enable Argenta to source and attract talent
  • Work with our People leaders to understand recruitment needs and develop plans to source and secure talent
  • Design and facilitate recruitment workshops to develop recruiting capabilities in our people leaders
  • Provide advice and interpretation to leadership around recruitment best practice in line with legislation

By nature, you’ll be a people person, driven by finding top quality talent and never compromising on culture fit. You’ll be someone who has the desire to continually improve systems, processes and the overall customer and candidate experience.

We pride ourselves on a great company culture built around a strong set of values (Commitment: make it; own it; meet it, Win As A Team, Driven By Innovation, Do it: Right First Time) this means you’ll be highly competent at what you do (the best in your field!), but also passionate about our company values and leading by example in living by them which are key to who we are and how we treat each other.

You'll join a fun, dynamic, and high-performing team where we genuinely support each other and are proud of the great stuff we do. If Argenta sounds like a company you see yourself fitting in, we would love to hear from you. When submitting your application, please take the time to put together a cover letter that reflects who you are and why you want this position, attach your CV and email it to recruitment@argentaglobal.com. For more information on what we do, check out our website at www.argentaglobal.com

Dispensary Operator

18/01/2018

We're looking for a reliable Operator for our dispensary to support the efficient operation of the warehouse and production, by accurately weighing, labelling and picking raw materials from the warehouse ready for use in production batches.

You will be someone who takes a pride in the accuracy of their work and can accurately follow written instructions in compliance with GMP. Your role will consist of checking that the correct raw ingredients are picked in the correct quantity or weight for each production batch and maintain accurate record keeping through our ERP system.

Your background, experience and personal attributes will include:

  • Relevant manufacturing or warehousing experience
  • Basic mathematical ability
  • As there is significant heavy lifting, you will need to be physically fit
  • Strong attention to detail
  • Strong focus on Health and Safety

This is a permanent full time role with typical working hours between of 6.00am to 2.30pm, Monday to Friday however you will have flexibility to work a later shift as production schedules and demands require.

On offer is a role with family friendly hours, a good hourly rate, and a great place to work in a small close knit team.

Please send a cover letter explaining why the position is of interest to you, attach your CV and send to recruitment@argenta.co.nz.

Warehouse Operator

07/02/2018

We are on the look out for an experienced Warehouse Operator to join our Warehousing team. Reporting to a team leader, your main responsibility will be to support the operation of the warehouse through the movement of incoming materials, material sampling and dispensing for Production.

Key responsibilities will include:

  • Receiving incoming materials including unloading, checking, storage and associated computer transactions
  • Dispatch including loading trucks and containers, associated computer transactions and moving stock around the warehouse
  • Sampling of Raw Materials including API and packaging materials in line with approved test methods, sampling plans, SOP’s and GMP
  • Maintaining a high level of housekeeping and cleanliness
  • Maintaining good written and verbal communication with internal customers
  • Operation of various fork hoists - note some duties are physically demanding and will require heavy lifting up to 20kgs

We’re looking for someone who can hit the ground running, so you MUST have:

  • A current and relevant fork hoist operating licence
  • Working experience within a manufacturing environment with a strong focus on quality would be preferable
  • Understanding of GMP would be preferable
  • Good computer literacy with the ability to pick up new packages and processes easily
  • Good understanding of health and safety issues
  • Excellent written and verbal English language communication skills

We’re looking for the right person, with the right experience whose values are similar to ours…so by nature you’ll be a committed, energetic team player, with a focus on quality. Attention to detail is imperative as we are regulated by the strictest of pharmaceutical standards. You’ll have a “Do it Right, First Time” mantra when conducting stock control and sampling and advising and implementing best practice.

This is a great opportunity for the right person, if you are interested, please email your CV to recruitment@argenta.co.nz

Quality Control Analyst

13/02/2018

Argenta QC is looking for an experienced Analyst to join our team. The QC Department supports our manufacturing business to ensure all incoming materials and finished products are tested to meet our quality standards and business needs.

We're looking for the right person, so you must be a someone who lives by our company values and isn't afraid to speak up and question the status quo, you are someone who enjoys being hands on, and it's second nature to help out others within your team and other departments.

Your background, experience and attributes will include:

  • Relevant tertiary qualification in either pharmaceutical science or chemistry
  • At least 2 years experience in a GMP environment in the pharmaceutical industry or similar using US or European Pharmacopoeia methods
  • A minimum of 2 years experience using HPLC and GC instrumentation is essential
  • Excellent time management abilities
  • Works effectively and collaboratively with other team members
  • Commitment to quality, excellence and continuous improvement

By nature you will be self motivated and have an investigative mind-set. You will possess excellent communication skills and the ability to impart knowledge and encouragement to others within the business. Your ability to identify and implement improvements and efficiencies in the team while ensuring required standards are maintained will see you succeed in this role.

Argenta has strongly embedded company values which is key to who we are and how we deliver, whether it's internal or external relationships. We actively develop our people, so there are career development opportunities available for the right candidate.

To register your interest in this role, please apply by putting together a cover letter which reflects who you are and why you want this position, attach your CV and email to recruitment@argenta.co.nz

Pharmaceutical Development Scientist

13/02/2018

Due to continued growth and lots of exciting projects coming on stream, we are looking for an additional formulation development scientist to add to our R&D team. This team conducts contract development projects on animal health products that range from pre-formulation activities through to manufacture of clinical trial material and all regulatory studies leading to registration and commercial supply. Having an international client base and exporting to over 60 countries, Argenta is unique in terms of the incredible variety of R&D projects we undertake, so this role is sure to keep the right person busy and challenged.

Your background could be from a small or global pharmaceutical company where you have been involved from conception to completion of the product development lifecycle, including overcoming all the obstacles along the way. You will be familiar with working in a cGMP environment and from your previous roles you will most likely have developed a number of products in various pharmaceutical dosage forms.

You will be dealing with multi-national pharmaceutical companies located all over the world, therefore building and maintaining “virtual” relationships is absolutely vital, as is being able to prepare high quality technical documents. By nature, you’ll be an energetic, driven person with a desire to continually improve systems, processes and the overall customer experience.

Your key responsibilities will include:

  • Leading the development of new formulations, products, analytical methods and manufacturing processes
  • Providing formulation expertise and technical input into development of new products
  • Generating, documenting, and reviewing technical data for client reports

Your background, experience and attributes will include:

  • A relevant tertiary qualification in science discipline, preferably Pharmacy/Pharmaceutical Sciences or Chemistry
  • Solid and liquid dose formulation development experience required
  • You may have a track record of authored scientific publications in peer reviewed journals
  • 2 - 5 years experience in the pharmaceutical industry or related field
  • A good understanding of the regulatory requirements involved in pharmaceutical product development
  • Excellent report writing skills
  • Strong relationship management and communication skills [written and verbal]

To apply please send your CV along with a cover letter to recruitment@argenta.co.nz

QA Officer

15/02/2018

Argenta is looking for an experienced QA Officer to join our Quality Assurance team on our morning shift. Your hours of work will be Monday to Friday 6am to 2.30pm, with flexibility as business needs require.

You will be working closely and collaboratively with the production personnel to provide manufacturing oversight, batch review and to ensure that products meet the required Quality Standards and cGMP compliance is maintained.

Key responsibilities will include:

  • Review of batch documents
  • Line clearances and in-process quality checks
  • Authoring and reviewing of procedures as required
  • Providing training to team members as required

Our internal timeframes are tight, so you will need have proven time management skills and be committed to providing a high level of internal customer service with a consultative and educational approach.

The key to your success is the ability to communicate effectively including an ability to negotiate and gain buy in from stakeholders; your strong and confident decision making ability; and your understanding of cGMP compliance in the manufacturing and testing of pharmaceutical products.

If you have 3 or more years’ experience in a similar position and enjoy a hands on role we would like to hear from you. To apply, please send your CV and a cover letter to recruitment@argenta.co.nz

QC Packaging Technician

22/02/2018

Our Quality Control team have a great opportunity for someone to join our packaging team. We’re looking for the right person, so we’re open to your background and experience, however you must be a someone who lives by our company values and isn’t afraid to speak up and question the status quo, you are someone who enjoys being hands on, and it’s second nature to help out others within your team.

Your key responsibilities will include:

  • Testing of packaging components according to approved test methods and GMP
  • Planning the testing of packaging components
  • Calibration of test equipment according to approved procedures
  • Maintain a high level of housekeeping and Good Laboratory Practice

Key attributes and experience:

  • An understanding and working experience within a GMP environment is preferable
  • Previous experience working in a laboratory environment preferred
  • An understanding of Health and Safety issues
  • Good written and verbal English language communication skills
  • Strong attention to detail, a focus on quality and a drive for doing things right first time

This is a great opportunity for the right person. If you are interested in applying or know someone who fits the bill, please email your CV and a covering letter to Recruitment@argenta.co.nz