Quality Control Engineer - Nestle
Bohemia, NY
About the Job
At Nestlé Health Science, we believe that nutrition, science, and wellness must merge, not collide. Here, we embrace the intrinsic connections of these three pillars, harnessing their collective strength to empower healthier lives. Our broad product portfolio includes renowned brands like Garden of Life®, Nature's Bounty®, Vital Proteins®, Orgain®, Nuun®, BOOST®, Carnation Breakfast Essentials®, Peptamen®, Compleat Organic Blends®, and more. We also have extensive pharmaceutical expertise, offering innovative medicines that aim to prevent, manage, and treat gastrointestinal and metabolic-related diseases.
At Nestlé Health Science, we bring our best for better lives. Our people are challenged to bring fresh, diverse views and make bold moves to empower healthier lives through nutrition. We know brilliant ideas can come from anyone, anywhere. Here we embrace the entrepreneurial spirit and collaborate with teams that champion focused and forward thinking. We are committed to fostering professional growth and celebrating the achievements of our people along the way. We offer dynamic career paths, robust development, opportunities to learn from talented colleagues around the globe, and benefits that support physical, financial, and emotional wellbeing.
Join us to innovate for impact and reimagine the future of health and nutrition for patients and consumers.
Position Summary :
As a Quality Control Engineer, you will have the responsibility of managing and performing root cause analyses and investigational studies for out-of-specification (OOS) and out-of-trend (OOT) results. This will involve collaborating with various teams to address problematic bulks and finished goods, ensuring that our products consistently meet the highest quality standards.
Additionally, you will have the exciting opportunity to serve as the QC representative for material review board (MRB) meetings. During these meetings, you will discuss non-conformance reports (NCRs) related to QC OOS investigations and ensure the prompt and effective execution of follow-up actions.
In addition to these critical responsibilities, you will oversee ISO 17025 compliance, record and evaluate data, prioritize your workload, and manage multiple projects in our state-of-the-art laboratory. Furthermore, you will have the chance to train and mentor other analysts, troubleshoot instruments, and actively contribute to the continuous improvement of our laboratory systems.
At our company, adherence to procedures and the maintenance of a safe environment are of utmost importance. We take great pride in our commitment to following industry-leading practices and ensuring the well-being of our valued team members. By joining our team, you will have the opportunity to make a significant impact on our ongoing success. Your contributions will directly influence the quality and integrity of our products, and you will be an integral part of a collaborative and supportive team that highly values innovation and excellence.
Key Responsibiltities :
+ Manages and performs root cause analyses and investigational studies for out-of-specification (OOS) and out-of-trend (OOT) results, including partnering with QC Analysts, Analytical Services, R&D, CTAG, Quality, and/or Operations to address problematic bulks and finished goods.
+ QC representative for material review board (MRB) meetings. Discuss non-conformance reports (NCRs) related to QC OOS investigations and responsible for executing any follow up actions required by QC.
+ Runs reports in various platforms to measure and monitor department metrics and KPI’s. Shares results and trends with QC management team.
+ Oversees ISO 17025 compliance and expansion for Analytical Lab.
+ Records data, performs calculations, evaluates and reports results. Performs peer review of data and provides critical
+ analysis of laboratory systems. Keeps management apprised of progress.
+ Prioritizes workload and meets scheduled timelines, including managing multiple priorities.
+ Follows and complies with all testing procedures, operating procedures, GMPs, and safety and health requirements, as applicable.
+ Demonstrates good housekeeping practices to minimize analytical mix ups, potential laboratory contamination and safety hazards.
+ At the discretion of QC Management, will be responsible for handling hazardous waste management. Understanding and handling of hazardous materials and waste using proper and safe techniques.
+ Trains and directs other analysts on laboratory practices, standard operating procedures, quality procedures, specific methods, and instrumentation.
+ Assists QC analysts with troubleshooting analytical instruments. Coordinates outside technical support as needed.
+ Coordinates and manages laboratory projects under Management guidance.
+ Reviews and approves product evaluation form (PEF) revisions.
+ Periodically performs duties of a higher position for the purpose of training and development.
+ Other responsibilities may be assigned as required based on business need or management decisions.
Experience and Educational Requirements :
+ Bachelor's degree in chemistry, biology, or a closely related natural science discipline is preferred. Significant analytical laboratory experience in lie of degree
+ A minimum of 6 years of experience in an analytical laboratory is strongly preferred
+ Experience in the pharmaceutical or nutraceutical industry strongly preferred
+ Expertise in at least one specific instrument or analyte group and possess the proficiency and skill set to operate various analytical instrumentation types, including HPLC, UPLC, UPLC-MS, GC, GC-MS, ICP-OES, or ICP-MS.
+ Familiarity with Empower software is preferred.
+ Proven ability to work collaboratively within teams, and maintain effectiveness during major changes in work tasks or the work environment.
+ Adherence to cGLP for all laboratory functions, including sample and standard preparation, analytical testing, analysis of results, investigation of Out of Specification (OOS) results, and reporting of test results is essential.
+ Advanced knowledge of analytical testing equipment, cGMP documentation, lab safety practices, and analytical techniques is expected, along with the ability to teach and train proper laboratory techniques to less experienced Chemists.
+ Continuously seeking ways to improve efficiency and quality while maintaining high standards.
+ Creativity and intellectual curiosity are valued, as the candidate should be willing to explore different and innovative approaches to overcome obstacles.
+ Please note that the work environment may involve exposure to powders, chemicals, and allergens such as peanuts, tree nuts, milk, dairy, eggs, wheat, gluten, soy, fish, and shellfish.
Requisition ID: 319244
The approximate pay range for this position is $75,000.00 to $90,000.00. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to knowledge, skills and abilities as well as geographic location.
Nestlé offers performance-based incentives and a competitive total rewards package, which includes a 401k with company match, healthcare coverage and a broad range of other benefits. Incentives and/or benefit packages may vary depending on the position. Learn more at About Us | Nestlé Careers (nestlejobs.com) (https://www.nestlejobs.com/nestle-in-the-us)
It is our business imperative to remain a very inclusive workplace.
To our veterans and separated service members, you're at the forefront of our minds as we recruit top talent to join Nestlé. The skills you've gained while serving our country, such as flexibility, agility, and leadership, are much like the skills that will make you successful in this role. In addition, with our commitment to an inclusive work environment, we recognize the exceptional engagement and innovation displayed by individuals with disabilities. Nestlé seeks such skilled and qualified individuals to share our mission where you’ll join a cohort of others who have chosen to call Nestlé home.
The Nestlé Companies are an equal employment opportunity and affirmative action employer seeking diversity in qualified applicants for employment. All applicants will receive consideration for employment without regard to race, ethnicity, color, gender, gender identity, age, religion, national origin, ancestry, disability, perceived disability, medical condition, genetic information, veteran status, sexual orientation, or any other protected status, as defined by applicable law. Prior to the next step in the recruiting process, we welcome you to inform us confidentially if you may require any special accommodations in order to participate fully in our recruitment experience. Contact us at accommodations@nestle.com or please dial 711 and provide this number to the operator: 1-800-321-6467.
This position is not eligible for Visa Sponsorship.
Review our applicant privacy notice before applying at https://www.nestlejobs.com/privacy
At Nestlé Health Science, we bring our best for better lives. Our people are challenged to bring fresh, diverse views and make bold moves to empower healthier lives through nutrition. We know brilliant ideas can come from anyone, anywhere. Here we embrace the entrepreneurial spirit and collaborate with teams that champion focused and forward thinking. We are committed to fostering professional growth and celebrating the achievements of our people along the way. We offer dynamic career paths, robust development, opportunities to learn from talented colleagues around the globe, and benefits that support physical, financial, and emotional wellbeing.
Join us to innovate for impact and reimagine the future of health and nutrition for patients and consumers.
Position Summary :
As a Quality Control Engineer, you will have the responsibility of managing and performing root cause analyses and investigational studies for out-of-specification (OOS) and out-of-trend (OOT) results. This will involve collaborating with various teams to address problematic bulks and finished goods, ensuring that our products consistently meet the highest quality standards.
Additionally, you will have the exciting opportunity to serve as the QC representative for material review board (MRB) meetings. During these meetings, you will discuss non-conformance reports (NCRs) related to QC OOS investigations and ensure the prompt and effective execution of follow-up actions.
In addition to these critical responsibilities, you will oversee ISO 17025 compliance, record and evaluate data, prioritize your workload, and manage multiple projects in our state-of-the-art laboratory. Furthermore, you will have the chance to train and mentor other analysts, troubleshoot instruments, and actively contribute to the continuous improvement of our laboratory systems.
At our company, adherence to procedures and the maintenance of a safe environment are of utmost importance. We take great pride in our commitment to following industry-leading practices and ensuring the well-being of our valued team members. By joining our team, you will have the opportunity to make a significant impact on our ongoing success. Your contributions will directly influence the quality and integrity of our products, and you will be an integral part of a collaborative and supportive team that highly values innovation and excellence.
Key Responsibiltities :
+ Manages and performs root cause analyses and investigational studies for out-of-specification (OOS) and out-of-trend (OOT) results, including partnering with QC Analysts, Analytical Services, R&D, CTAG, Quality, and/or Operations to address problematic bulks and finished goods.
+ QC representative for material review board (MRB) meetings. Discuss non-conformance reports (NCRs) related to QC OOS investigations and responsible for executing any follow up actions required by QC.
+ Runs reports in various platforms to measure and monitor department metrics and KPI’s. Shares results and trends with QC management team.
+ Oversees ISO 17025 compliance and expansion for Analytical Lab.
+ Records data, performs calculations, evaluates and reports results. Performs peer review of data and provides critical
+ analysis of laboratory systems. Keeps management apprised of progress.
+ Prioritizes workload and meets scheduled timelines, including managing multiple priorities.
+ Follows and complies with all testing procedures, operating procedures, GMPs, and safety and health requirements, as applicable.
+ Demonstrates good housekeeping practices to minimize analytical mix ups, potential laboratory contamination and safety hazards.
+ At the discretion of QC Management, will be responsible for handling hazardous waste management. Understanding and handling of hazardous materials and waste using proper and safe techniques.
+ Trains and directs other analysts on laboratory practices, standard operating procedures, quality procedures, specific methods, and instrumentation.
+ Assists QC analysts with troubleshooting analytical instruments. Coordinates outside technical support as needed.
+ Coordinates and manages laboratory projects under Management guidance.
+ Reviews and approves product evaluation form (PEF) revisions.
+ Periodically performs duties of a higher position for the purpose of training and development.
+ Other responsibilities may be assigned as required based on business need or management decisions.
Experience and Educational Requirements :
+ Bachelor's degree in chemistry, biology, or a closely related natural science discipline is preferred. Significant analytical laboratory experience in lie of degree
+ A minimum of 6 years of experience in an analytical laboratory is strongly preferred
+ Experience in the pharmaceutical or nutraceutical industry strongly preferred
+ Expertise in at least one specific instrument or analyte group and possess the proficiency and skill set to operate various analytical instrumentation types, including HPLC, UPLC, UPLC-MS, GC, GC-MS, ICP-OES, or ICP-MS.
+ Familiarity with Empower software is preferred.
+ Proven ability to work collaboratively within teams, and maintain effectiveness during major changes in work tasks or the work environment.
+ Adherence to cGLP for all laboratory functions, including sample and standard preparation, analytical testing, analysis of results, investigation of Out of Specification (OOS) results, and reporting of test results is essential.
+ Advanced knowledge of analytical testing equipment, cGMP documentation, lab safety practices, and analytical techniques is expected, along with the ability to teach and train proper laboratory techniques to less experienced Chemists.
+ Continuously seeking ways to improve efficiency and quality while maintaining high standards.
+ Creativity and intellectual curiosity are valued, as the candidate should be willing to explore different and innovative approaches to overcome obstacles.
+ Please note that the work environment may involve exposure to powders, chemicals, and allergens such as peanuts, tree nuts, milk, dairy, eggs, wheat, gluten, soy, fish, and shellfish.
Requisition ID: 319244
The approximate pay range for this position is $75,000.00 to $90,000.00. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to knowledge, skills and abilities as well as geographic location.
Nestlé offers performance-based incentives and a competitive total rewards package, which includes a 401k with company match, healthcare coverage and a broad range of other benefits. Incentives and/or benefit packages may vary depending on the position. Learn more at About Us | Nestlé Careers (nestlejobs.com) (https://www.nestlejobs.com/nestle-in-the-us)
It is our business imperative to remain a very inclusive workplace.
To our veterans and separated service members, you're at the forefront of our minds as we recruit top talent to join Nestlé. The skills you've gained while serving our country, such as flexibility, agility, and leadership, are much like the skills that will make you successful in this role. In addition, with our commitment to an inclusive work environment, we recognize the exceptional engagement and innovation displayed by individuals with disabilities. Nestlé seeks such skilled and qualified individuals to share our mission where you’ll join a cohort of others who have chosen to call Nestlé home.
The Nestlé Companies are an equal employment opportunity and affirmative action employer seeking diversity in qualified applicants for employment. All applicants will receive consideration for employment without regard to race, ethnicity, color, gender, gender identity, age, religion, national origin, ancestry, disability, perceived disability, medical condition, genetic information, veteran status, sexual orientation, or any other protected status, as defined by applicable law. Prior to the next step in the recruiting process, we welcome you to inform us confidentially if you may require any special accommodations in order to participate fully in our recruitment experience. Contact us at accommodations@nestle.com or please dial 711 and provide this number to the operator: 1-800-321-6467.
This position is not eligible for Visa Sponsorship.
Review our applicant privacy notice before applying at https://www.nestlejobs.com/privacy
Source : Nestle
