Senior Analytical Chemist
1 month ago
**Opportunity to join a brand-new team in our QC lab working night shift hours**
**Great opportunity for an experienced Chemist to taken on a 2IC role**
**Permanent role Mon - Fri on night shift 10pm-6.30am**
**Be part of a global researcher & manufacturer of animal health pharmaceuticals**
**About us**
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 the uniqueness of our vision and our people. Argenta now has operations across the globe with locations in New Zealand, the United States, Scotland, Germany and Spain with 600+ employees and still growing
**About the role**
With a significant increase in production orders at the Manurewa site, there is a critical need to create a new shift in the QC laboratory - the Night Shift. The Quality Control team will support our manufacturing business to ensure raw materials and finished products are tested to meet the highest level of quality standards and business requirements.
This role is unique as the night shift will not only include regular analytical testing but will also be responsible for release to fill testing, QA activities such as line clearances, equipment calibration & maintenance, investigations and managing stock of glassware and consumables.
You will also be expected to be involved in health and safety practices such as fire warden duty, first aider, certified spill response as well as identifying critical risks in your environment.
**About you**
Therefore, we’re looking for someone who is not only capable from a technical perspective but is adaptable and flexible as a member of a small team. By nature, you are a solutions-orientated team player that takes a proactive approach to their work.
**Your background, experience and attributes will include**:
- Relevant tertiary qualification in chemistry
- Minimum 3-years’ experience in a GMP environment in the pharmaceutical industry
- Proficiency in analytical testing such as HPLC/IR/AAS is preferable
- Able to strictly follow the standard operating procedure
- Ability to work under pressure, multitask and manage your time effectively
- Proven attention to detail, quality focused and a willingness to learn and improve
- Commitment to quality, standards, and integrity
**Why us?**
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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