Stability Coordinator at Argenta

Auckland, Auckland, New Zealand -

Full Time

Start Date

Immediate

Expiry Date

15 Feb, 26

Salary

0.0

Posted On

17 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Time Management, Organisational Skills, Analytical Testing, Chemistry Techniques, Communication Skills, Team Player, Autonomous Work, Attention to Detail, Problem Solving, Physical Fitness

Industry

Pharmaceutical Manufacturing

Description

Stability Coordinator . . . . . . .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . New opportunity in Stability & Validation team for Chemistry graduate to showcase their time management and organisational skills. Day shift role, Mon-Fri, South Auckland location & onsite parking Varied role with analytical testing included Opportunity for growth within pharmaceutical business 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 almost 500+ employees globally. About the role: Due to the departure of a team member, we’ve got a great opportunity for a permanent full-time Stability Coordinator to join the Stability and Validation team. This role is responsible for the effective management and coordination of all GMP stability studies at the Auckland site. Working closely with Production, Quality Control and our external clients, no two days will be the same. You will be kept busy with tasks including but not limited to: Preparing stability programs, maintaining schedules, and assisting with stability pulls according to protocols. Creating and updating stability specifications, protocols, reports, records, and SOPs as required. Undertaking analytical testing such as physical and wet chemistry techniques. Scheduling preventative maintenance, cleaning, and annual spatial qualifications of our stability chambers. Preparing invoices, raising purchase orders, and dispatching samples as required. About you: This is a great entry level role for a Chemistry graduate to kick-off their career in the pharmaceutical industry. This role has several future growth opportunities including in the Validation and Quality Control departments. To be successful in this role, you will be described as a team player but also able to work autonomously with limited supervision. Other skills you will bring to the role include: BSc Graduate with a major in Chemistry. Full drivers licence and own vehicle as there will be some occasional travel. Strong time management and organisation skills with attention to Excellent verbal and written Physically fit with no injuries and able to carry samples weighing up to Able to work well under pressure and have a solutions-orientated mindset for Please note that there will be a pre-employment medical completed as a condition of employment. This role is only open to those who already have the right to work in New Zealand. Why Join Us? On offer is an opportunity to work for a unique and rapidly expanding business where your input will be valued, your skills will be developed, and you will be rewarded with a competitive salary as well as comprehensive insurance plans. If you are a recent Chemistry graduate and looking for a challenging opportunity to kick start your career, we want to hear from you! To apply, please submit your CV and a cover letter outlining your experience and motivation for the role.

Responsibilities

The Stability Coordinator is responsible for managing and coordinating all GMP stability studies at the Auckland site. This includes preparing stability programs, maintaining schedules, and undertaking analytical testing.