Quality Assurance Technical Associate (Cary)

Join a Science-Led Consumer Healthcare Pioneer on an Exciting Growth Journey

Are you ready to be part of something extraordinary? At Alliance, we're a dynamic, science-led consumer healthcare organisation specialising in advanced skincare solutions and vitamins, minerals & supplements (VMS). Backed by innovation and driven by purpose, we're on an exciting journey of transformation and growth expanding our reach, enhancing our brands, and bringing cutting-edge products to more consumers across the globe.

As we continue to evolve, were looking for passionate, curious, and driven individuals to join us. If youre excited by the opportunity to shape the future of health and wellness in a fast-paced, entrepreneurial environment this is your moment.

Were looking for a Quality Assurance Technical Associate (known internally as a Quality Technical Scientist) with a mix of quality assurance expertise and technical curiosity, as you will work closely with cross-functional teams and external partners to keep products on the market, support product transfers, and drive technical projects forward.

This quality role works with our contract manufacturers across our portfolio of consumer healthcare and pharma products in the US to support and execute technical projects.

This is not a scientist role where you will be working in the lab testing, or directly working on batches in a factory. You will work in our Cary office a minimum of 2 days a week reporting to the US Quality Manager and must be comfortable working in a small quality team, be accountable and able to thrive in a collaborative, fast-moving environment

What were looking for

• A bachelors degree (scientific / technical discipline preferred).
• Quality assurance experience with a Contract Manufacturer within pharma or consumer healthcare would be the ideal
• Experience working with FDA-regulated consumer products (dietary supplements, OTC drugs, medical devices, cosmetics, or food).
• Audit experience and / or ASQ CQA / CQE certification (or interest in pursuing).
• Knowledge in the medical device space ISO13485
• Quality system management experience
• Experience working with FDA-regulated consumer products (dietary supplements, OTC drugs, medical devices, cosmetics, or food).
• A risk assessment subject matter expert
• Ability to perform investigations, driving to root cause and then help manage the CAPA that result from those investigations
• Reviewed and approved validation / verification documentation
• A change control project manager or owner
• Knowledge of GMP, GLP, and / or GCP regulations.
• Strong attention to detail with the ability to interpret complex technical information.
• Excellent communication and collaboration skills across functions and geographies.
• A proactive, problem-solving mindset and willingness to think outside the box.

What youll be doing

Why join us?

At Alliance, youll be part of a purpose-driven business that empowers people. We offer a supportive, collaborative culture with real opportunities to grow your career as we grow our brands.

We also offer great benefits

If you are looking to make a difference and be part of something exciting, wed love to hear from you