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Supv., Quality Assurance (i) at The Bountiful Company

Posted in Other 30+ days ago.

Location: Leonia, New Jersey





Job Description:



Job Description




Company Description

The Bountiful Company is a global leader in health and wellness, living at the intersection of science and nature. As a manufacturer, marketer and seller of vitamins, minerals, herbals, supplements, protein bars and powders, we are focused on enhancing the health and wellness of people's lives. The brands of The Bountiful Company are some of the most trusted in the world including Nature's Bounty, Solgar, Pure Protein, Osteo Bi-Flex, Puritan's Pride, Sundown, Body Fortress, MET-Rx, Ester-C and Dr.Organic.

Inclusion and Diversity in the workplace matters at The Bountiful Company. This includes being focused on retaining and recruiting a diverse workforce and building a culture of inclusivity. Our goal is to create a place where people feel respected, valued and able to bring their authentic selves to work each day.

Did we mention that we also offer excellent benefits, competitive compensation and a progressive, healthy company culture? If you've ever spent your workdays watching the clock, you know how important a positive work environment is for a person's well-being. The Bountiful Company is committed to supporting wellness in all forms. And when it comes to wellness, nature is a pretty good place to start.



Job Description

Under the direction of the Quality Manager, the QA Quality Engineer provides overall quality support for manufacturing and quality departments to improve overall product quality. This is an excellent opportunity for an individual with strong engineering, quality and operations background. The Quality Engineer will participate in quality improvement initiatives to reduce defects and quality issues, and make recommendations to improve the production process based on findings from quality analysis. Collaboration across multiple disciplines is critical for the successful implementation of the corrective actions. This role will interface closely with other cross-functional groups such as our Manufacturing, Engineering, R&D and Quality.

Responsibilities include, but are not limited to:


  • Sets and monitors SPC data to ensure delivery of consistent quality. Utilize basic statistical tools to analyze for trends or issues.

  • Develops and analyzes statistical data and specifications to establish product and process capabilities (Cp/Cpk).

  • Identify, develop, and implement process controls to meet customer/specification requirements.

  • Develops/authors verification and validation protocols (i.e. Validation Plans, IQ/OQ/PQ protocols, validation summary reports).

  • Assists and coordinates equipment, cleaning and process validations.

  • Participate in and support the maintenance of the Quality Management System and Maintain Quality Department business metrics.

  • The Quality Engineer will lead and / or support thorough investigations of quality issues (CAPA's, Non-Conformances, Audit Observations, etc.) ensuring effective corrective and / or preventive actions occur.

  • Analyze plant controllable consumer complaint data to identify all types of quality problems and perform root cause analysis

  • Participate in cross-functional teams on process control, improvement, and optimization projects; participate in other continuous improvement projects.

  • Performs assessments of any given quality system to determine the effectiveness and dependability of such system.

  • Ensure all quality specifications are met for any given product or procedure and suggests methods to bring equipment and work procedures into compliance with quality control standards.

  • Direct support of project activities and all other associated Quality functions.

  • Assist in investigations, which includes interactions with vendors or Supplier Development and Procurement Management for issues associated with raw materials and components.





Job Requirements



  • 5+ years of experience in the food, pharmaceutical and or supplement industry preferred

  • Knowledge of regulatory requirements that affect the dietary supplement and/or pharmaceutical manufacturing business, preferred

  • Bachelor's in Pharmaceutical, Food Science, Chemical Engineering, Chemistry or other Science related field preferred or other closely related discipline with extensive significant experience can be considered in lieu of a Bachelor's degree

  • ASQ CQE or CQM preferred

  • Must be proficient with PC programs, i.e. Microsoft Office (Word, Excel, PowerPoint)

  • Problem solving and statistical skills using quality tools (Pareto analysis, statistical process control, multi-variant DOE etc.).

  • AS400 Knowledge desirable

  • Knowledge of regulatory and GMP compliance requirements such as 21 CFR Part 111, HACCP, HARPC preferred

  • SQF practitioner / FSSC/ BRC/ ISO experience preferred

  • Strong analytical skills; able to use data, communicate key trends, develop and execute continuous improvement plans.

  • Ability to work with cross-functional groups to implement improvements

  • Strong organizational skills; ability to managemultiple tasks and work well under pressure

  • Demonstrated ability to work effectively with individuals at alllevels of the organization.

  • Demonstrated ability to use influencing skills to accomplish goalsand objectives.



Ref # POS000004265







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