Permanent full-time Stability Coordinator role in South Auckland, managing GMP stability studies and analytical testing for a global animal health pharmaceutical company.
Your Role
Key responsibilities include :
- Managing and coordinating all GMP stability studies at the Auckland site
- 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
- Scheduling preventative maintenance, cleaning, and annual spatial qualifications of stability chambers
- Preparing invoices, raising purchase orders, and dispatching samples as required
- Collaborating closely with Production, Quality Control, and external clients
About You
The company is looking for :
BSc Graduate with a major in ChemistryFull driver’s licence and own vehicle for occasional travelStrong time management and organisational skills with attention to detailExcellent verbal and written communication skillsPhysically fit and able to carry samples weighing up to a specified amountAbility to work well under pressure with a solutions-oriented mindsetTeam player who can also work autonomously with limited supervisionRight to work in New ZealandWillingness to complete a pre-employment medicalCompensation & Benefits
Competitive salaryComprehensive insurance plansOnsite parkingDay shift role, Monday to FridayTraining & Development
Opportunity to develop skills within a unique and rapidly expanding pharmaceutical business.
Career Progression
Future growth opportunities within the Validation and Quality Control departments.
How to Apply
Submit your CV and a cover letter outlining your experience and motivation for the role.
This job may close before the stated closing date; you are encouraged to apply as soon as possible
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