Job Description

About us:

At Argenta, we're more than a company -- we're a global team dedicated to healthier animals. Founded in 2006 by a New Zealand chemist with an entrepreneurial mindset, our vision is simple yet powerful: "Healthy Animals, Let's Make it Happen Together." We partner with clients in Research, Development & Innovation (RD&I) and Manufacturing to produce pharmaceuticals for both farm and companion animals.



Argenta now has operations across the globe with locations in New Zealand, the United States, Scotland, Germany, and Spain with 900+ employees globally.

About the Role:

Argenta is currently looking to fill the role of

AS&T Analyst

onsite at our

Dundee

location. This role will conduct non- routine Analytical Services for the site including (1) Analytical method transfers into Quality, (2) Analytical method evaluations and validation, (3) method innovation (4) pharmacopeial compliance, (5) sample management / logistics.

Key Accountabilities:

Evaluate the performance of analytical methods identifying continuous improvement opportunities Performs method development and validation testing to maintain and improve the compliance status of the analytical methods used in the quality control labs. Perform analytical method transfer testing required to successfully transfer analytical methods and techniques into the Quality control labs. Perform analytical method verification activities to ensure that analytical packages are available and maintained to demonstrate Pharmacopeial compliance Provide the analytical support for the Manufacturing Science and Technology group to support manufacturing process development & validation. Provide analytical troubleshooting support for investigations which require non routine / specialized services Comply with all company local and global policies including but not limited to Quality frameworks, Values and Behaviours and health, safety and environment (HSE) policies.

Perform any other duties or serve in such other capacity as may be determined by Company management.

Qualifications:

HNC or Degree in Science (Chemistry, Pharmacy, Chemical Engineering etc.)

Knowledge/Experience:

Minimum 1 year Experience in cGMP & Global regulatory environment Ability to multi-task and adapt to changing business requirements in dynamic manufacturing environment Demonstrated technology skills i.e. equipment, instrumentation & computers Effective technical writing skills e.g. reports; SOPs and change control 1 - 3 years experience - Proven track record in the performance of a variety of analytical techniques especially HPLC, 1 - 3 years experience - Demonstrated experience in method development, method validation, troubleshooting and analytical technology transfer Effective communication skills both written and verbal

Demonstrated continuous improvement mind-set