Analytical Supervisor

2 weeks ago


Auckland City, New Zealand Argenta Full time

**Analytical Supervisor**

**Have a passion for manufacturing or pharmaceuticals and all things Quality?**
- Are you a delivery focused people leader who loves the technical side?
- Global animal health pharmaceutical manufacturer
- Successful and innovative business with a unique Kiwi origin

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, and Germany with almost 500 employees globally - and continuing to grow

We are currently looking for someone to lead our Finished Products team dedicated to the testing of commercial animal pharmaceuticals and stability products. Reporting directly to the Quality Control Manager, you will lead a team of analysts, review chemists and technical leads. The key focus areas are to lead, develop and empower your team while working with other teams and departments to ensure the efficient release of products in compliance with GMP standards and regulations.

We're looking for someone who can build strong, collaborative working relationships across multiple departments, while also maintaining a commitment to driving a quality culture within the organisation. You will have strong leadership skills with proven success in leading a team with flexibility, the ability to multitask and manage time effectively.

**Your key responsibilities will include**:

- Ensuring the team contributes to our strategy of “Right First Time” products for our customers
- Growing and developing the team to strengthen capability
- Providing active involvement in laboratory investigations
- Driving continuous improvement within your team
- Championing a quality culture across the site
- Leading Health and Safety initiatives

**Your background, experience and attributes will include**:

- Relevant tertiary qualification
- A minimum of 3 years working experience within a cGMP environment
- Demonstrated people leadership experience
- Exceptional verbal and written communication skills, being able to collaborate across multiple teams
- Highly organised with the ability to be flexible and resilient to change
- Proven analytical and logical problem-solving capabilities
- Proven leadership skills with the ability to delegate and develop your people

On offer is an opportunity to work for a successful 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, life, medical and income insurance.


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