Jobs · Manufacturing · Maine

Quality Manager

ElleVet Sciences · South Portland, ME · 3 mo ago
ManufacturingFull-time

About Us

At ElleVet Sciences, we are committed to improving the lives of pets through science and innovation. As a leader in veterinary health, we are dedicated to providing effective, science-backed solutions for pets. Our mission is to combine cutting-edge science with care and compassion to create products that make a real difference. The secret to our success is simple, and the same as our company philosophy:

  • Do the right thing
  • Do what is best for animals
  • Trust science
  • Always be learning

Our comprehensive benefits package includes the following:

  • Health, dental, and vision insurance
  • Health savings account (HSA)
  • 401(k) with company match
  • 20 days of paid time off (PTO) per year & 9 paid company holidays
  • Basic and voluntary life insurance
  • Short and long-term disability insurance
  • Employee discount on our products
  • Flexible schedules and room for internal growth
  • Dog friendly office

Who We Are Seeking

  • Experience managing a quality program, including QA & QC, in a manufacturing environment, preferably in foods, supplements, or pharmaceuticals.
  • Ability to drive quality achievement and performance improvement throughout the organization.
  • Knowledge of quality control standards and testing methodologies.
  • Understanding of cGMP.
  • Experience successfully managing an audit process.
  • Data analysis and statistical aptitude.
  • Communicate effectively, both verbal and written, with all internal organization departments, suppliers, and regulatory authorities.
  • Able to assess risk and provide solutions, as needed.
  • Highly organized with strong attention to detail.
  • Ability to thrive in a dynamic work environment with rapidly changing priorities.
  • Bachelor’s degree in science.
  • Laboratory experience is a plus.

What You Will Do

  • Develop, implement, and maintain quality procedures, policies, and QMS framework.
  • Train employees and ensure compliance with all cGMP policies across departments.
  • Lead independent facility NASC audits once every two years.
  • Ensure accurate recording of quality specifications and testing results.
  • Oversee hold-point releases once all QMS functions have been completed.
  • Hands on experience in production processes to aid in continuous improvement projects.
  • Assist in the creation, implementation, and maintenance of SOPs.
  • Develop and manage non-conformance, deficiencies, and reporting programs, including root cause analysis and corrective action planning.
  • Oversee and maintain the quality department budget.

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