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Quality Engineer (I)

Job Description

Company Description

The Bountiful Company, a Nestlé Health Science Company, is a pure play branded leader in global nutrition, living at the intersection of science and nature. As a manufacturer, marketer and seller of vitamins, minerals, herbal and other specialty supplements, and active nutrition products, we are focused on enhancing the health and wellness of people’s lives. The Bountiful Company’s portfolio of trusted brands includes Nature's Bounty®, Solgar®, Osteo Bi-Flex®, Puritan’s Pride®, Sundown® and Ester-C®.

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

The Quality Engineer provides overall quality support for manufacturing and quality departments to improve overall Solid-Dosage product quality. This is an excellent opportunity for an individual with strong engineering, quality and operations background. 

Responsibilities include, but are not limited to:

  • 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, which is critical for the successful implementation of the corrective actions.
  • Interface closely with other cross-functional groups such as our Manufacturing, Engineering, R&D and Quality.
  • 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.
  • Lead and / or support thorough investigations of quality issues (CAPA’s, Non-Conformances, Audit Observations, etc.) ensuring effective corrective and / or preventive actions occur.
  • 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. 
  • Ensures 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

Qualifications

  • 5+ years of experience in the food, nutraceutical, pharmaceutical and or supplement industry preferred.
  • Ideal candidate has experience with solid-dose techniques (including Mixing, Blending, Tableting, Encapsulating and Coating).
  • 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.).
  • Knowledge of regulatory and GXP compliance requirements such as 21 CFR Part 111, HACCP, HARPC preferred
  • Strong analytical skills; able to use data, communicate key trends, develop and execute continuous improvement plans.
  • Six Sigma Green Belt preferred
  • Ability to work with cross-functional groups to implement improvements
  • Strong organizational skills; ability to manage multiple tasks and work well under pressure
  • Demonstrated ability to work effectively with individuals at all levels of the organization.
  • Demonstrated ability to use influencing skills to accomplish goals and objectives
  • Capable of lifting 40 lbs.
  • Work environment may be exposed to powders, chemicals and allergens (peanuts, tree nuts, milk, dairy, eggs, wheat, gluten, soy, fish and shellfish)

Additional Information

Job Snapshot

Location US-NY-Bohemia
Employment Type Full-Time
Pay Type Year
Pay Rate N/A
Store Type Engineering & Aerospace, Other
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Company Overview

The Bountiful Company

The Bountiful Company, a Nestlé Health Science Company, is a pure play branded leader in global nutrition, living at the intersection of science and nature. As a manufacturer, marketer and seller of vitamins, minerals, herbal and other specialty supplements, and active nutrition products, we are focused on enhancing the health and wellness of people’s lives. The Bountiful Company’s portfolio of trusted brands includes Nature's Bounty®, Solgar®, Osteo Bi-Flex®, Puritan’s Pride®, Sundown® and Ester-C®. The Bountiful Company employs more than 4,000 people worldwide and has manufacturing, packaging, warehouse, distribution and administrative facilities throughout the United States, Canada and United Kingdom. The company also maintains offices overseas in China, Spain, South Africa and New Zealand. Learn More

Contact Information

US-NY-Bohemia
Snapshot
The Bountiful Company
Company:
US-NY-Bohemia
Location:
Full-Time
Employment Type:
Year
Pay Type:
N/A
Pay Rate:
Engineering & Aerospace, Other
Store Type:

Job Description

Company Description

The Bountiful Company, a Nestlé Health Science Company, is a pure play branded leader in global nutrition, living at the intersection of science and nature. As a manufacturer, marketer and seller of vitamins, minerals, herbal and other specialty supplements, and active nutrition products, we are focused on enhancing the health and wellness of people’s lives. The Bountiful Company’s portfolio of trusted brands includes Nature's Bounty®, Solgar®, Osteo Bi-Flex®, Puritan’s Pride®, Sundown® and Ester-C®.

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

The Quality Engineer provides overall quality support for manufacturing and quality departments to improve overall Solid-Dosage product quality. This is an excellent opportunity for an individual with strong engineering, quality and operations background. 

Responsibilities include, but are not limited to:

  • 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, which is critical for the successful implementation of the corrective actions.
  • Interface closely with other cross-functional groups such as our Manufacturing, Engineering, R&D and Quality.
  • 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.
  • Lead and / or support thorough investigations of quality issues (CAPA’s, Non-Conformances, Audit Observations, etc.) ensuring effective corrective and / or preventive actions occur.
  • 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. 
  • Ensures 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

Qualifications

  • 5+ years of experience in the food, nutraceutical, pharmaceutical and or supplement industry preferred.
  • Ideal candidate has experience with solid-dose techniques (including Mixing, Blending, Tableting, Encapsulating and Coating).
  • 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.).
  • Knowledge of regulatory and GXP compliance requirements such as 21 CFR Part 111, HACCP, HARPC preferred
  • Strong analytical skills; able to use data, communicate key trends, develop and execute continuous improvement plans.
  • Six Sigma Green Belt preferred
  • Ability to work with cross-functional groups to implement improvements
  • Strong organizational skills; ability to manage multiple tasks and work well under pressure
  • Demonstrated ability to work effectively with individuals at all levels of the organization.
  • Demonstrated ability to use influencing skills to accomplish goals and objectives
  • Capable of lifting 40 lbs.
  • Work environment may be exposed to powders, chemicals and allergens (peanuts, tree nuts, milk, dairy, eggs, wheat, gluten, soy, fish and shellfish)

Additional Information

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