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Quality Technical Scientist

Alliance Pharmaceuticals

  • Date Posted

    Today

    New!
  • Remote Work Level

    Hybrid Remote

  • Location

    Hybrid Remote in Cary, NC

  • Salary

    We're sorry, the employer did not include salary information for this job.

  • Benefits

    Health Insurance Dental Insurance Vision Insurance Life Insurance Retirement Savings Disability Paid Holidays Paid Time Off Community Service

  • Categories

    PharmaceuticalQASoftware Engineer

  • Job Type

    Freelance

  • Career Level

    Experienced

  • Travel Required

    No specification

  • Education Level

    Bachelor's/Undergraduate Degree

About the Role

Job Description:

Job Title:Quality Technical Scientist
Reports to:Quality Manager - US
Team:Global Quality
-Location:Cary, NC
Contract type:Permanent
Work set up:Hybrid - 2 days onsite

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, we're looking for passionate, curious, and driven individuals to join us. If you're excited by the opportunity to shape the future of health and wellness in a fast-paced, entrepreneurial environment - this is your moment. We're 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 crossfunctional 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 we're looking for

  • A bachelor's 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 you'll be doing

  • Provide quality assurance support for consumer healthcare products distributed in North America.
  • Oversee product release activities, ensuring compliance with specifications and procedures.
  • Manage deviations and nonconformances, including root cause analysis and corrective/preventive actions.
  • Write, update, and train on Standard Operating Procedures.
  • Lead day-to-day activities for technical product transfers (including stability and validation programs).
  • Deliver on assigned technical projects with cross-functional and external teams.
  • Maintain product specifications for both new and existing products.
  • Support audits and inspections, contributing to continuous improvement.

Why join us?

At Alliance, you'll be part of a purposedriven 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

  • 25 days holiday per annum + one celebration day + one volunteering day + plus 9 bank

holidays (pro rata)

  • 401k retirement benefits (employer match is 4% with immediate vesting), employer paid life/

disability/AD&D insurance, dental and eye care and subsidized employee medical insurance

coverage

  • Comprehensive benefits include a 4% employer matched 401(k) with immediate vesting, fully paid dental/vision, life, disability, and AD&D insurance, plus subsidized medical coverage.

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

 

Apply