INTERCOS
Quality Control Manager
INTERCOS, West Nyack, New York, United States, 10994
About UsImagine the innovation and expertise behind the world's leading cosmetic brands, brought to you by a distinguished Italian company with a legacy of excellence. Since 1972, Intercos Group has been at the forefront of color cosmetics, pencils, nail polish, skincare, and personal care products. We pride ourselves on being the only cosmetics manufacturer that combines top-tier quality and advanced technology with a global reach and a personalized touch.With 15 commercial offices and 15 production facilities across 12 countries, Intercos Group brings a local approach to a global stage. We continually set the standard for beauty, crafting exceptional product lines for brands worldwide. As one of the largest suppliers in the cosmetics industry, we are a leading force in the research, development, and production of beauty products, shaping the future of the industry with every season.Position SummaryThe
Quality Control Manager
is responsible for all aspects of Quality measurement, product inspection and in-process testing in
West Nyack, NY . The primary responsibility is to ensure that Quality Control personnel perform the required inspection accurately and as specified by the appropriate quality documentation. This position will allocate resources to efficiently maintain orders on schedule. The Quality Control Manager is responsible for the training, the discipline and morale of the staff and will report to the VP of Quality/Reporting.Essential FunctionsQuality Control - Product Inspection and ReleaseTesting of materials required to produce a finished product and the final product to confirm compliance to issued specifications.QC Inspectors are responsible for (but not limited to)Physical - Dimensions, Hardness, Drop test, tap test, net weight; Visual - Color (e.g. color matching), Appearance; Sensory - Odor, TextureProduct DispositionDetermine final disposition of all productsResponsible for approving and rejecting all batchesManagement of Product Hold and DispositionQuality Control Documentation/Samples for ClientsConversion of Product Specifications to Production Line Documentation (checklists, forms)Finished Product Documentation to be issued to Clients, (e.g. COA)Pre-Shipment Samples to ClientsManagement of Documents and Product Samples Retention RequirementsRecords /Documentation review and sign off for OTC ProductsMonitor and confirm production operations conforming to specifications or requirementsLine ClearanceCritical Process Parameter Line Set UpManagement of StaffManage QC work schedules; accountable for QC team's work hoursResponsible for allocating QC personnel to the production linePerform staff performance evaluationResponsible for the training of the QC personnel, the discipline and morale of the staff.Perform other duties and projects as assigned.Job QualificationsBachelor's degree in Applied Sciences or Engineering (e.g., Biology, Chemistry, Physics, or a related field).At least 5 years of experience in Quality Management, QA, or QC.Proven expertise in Quality Management.Familiarity with Quality Systems, including GMP and GLP, in an FDA-regulated industry.Strong critical thinking and problem-solving skills, with the ability to identify and resolve issues promptly, analyze information effectively, and develop alternative solutions.Excellent interpersonal and communication skills.Capable of managing and developing staff.Collaborative team player.Self-motivated and proactive.Job BenefitsHealth Insurance:
Comprehensive medical, dental, and vision coverageRetirement Plans:
401(k) plan, often with company matchingLife Insurance:
Coverage for employees in the event of death or disabilityPaid Time Off (PTO):
Vacation days, sick leave, and personal daysHolidays:
Paid company holidays and floating holidaysProfessional Development:
Training programs and opportunities for career advancementPerformance Bonuses:
Annual merit increase and/or bonus based on individual performanceCompany Events:
Team-building activities, social events, and company outingsEmployee Assistance Programs (EAPs):
Confidential counseling and support services for personal and professional issues.EEOIntercos Group is committed to creating a diverse and inclusive workplace where everyone is valued and respected. We believe that a wide range of perspectives and experiences enhances our innovation and success. We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other legally protected status. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to any of these characteristics. We are dedicated to providing a work environment that is free from discrimination and harassment and promotes equal opportunity for all.
Quality Control Manager
is responsible for all aspects of Quality measurement, product inspection and in-process testing in
West Nyack, NY . The primary responsibility is to ensure that Quality Control personnel perform the required inspection accurately and as specified by the appropriate quality documentation. This position will allocate resources to efficiently maintain orders on schedule. The Quality Control Manager is responsible for the training, the discipline and morale of the staff and will report to the VP of Quality/Reporting.Essential FunctionsQuality Control - Product Inspection and ReleaseTesting of materials required to produce a finished product and the final product to confirm compliance to issued specifications.QC Inspectors are responsible for (but not limited to)Physical - Dimensions, Hardness, Drop test, tap test, net weight; Visual - Color (e.g. color matching), Appearance; Sensory - Odor, TextureProduct DispositionDetermine final disposition of all productsResponsible for approving and rejecting all batchesManagement of Product Hold and DispositionQuality Control Documentation/Samples for ClientsConversion of Product Specifications to Production Line Documentation (checklists, forms)Finished Product Documentation to be issued to Clients, (e.g. COA)Pre-Shipment Samples to ClientsManagement of Documents and Product Samples Retention RequirementsRecords /Documentation review and sign off for OTC ProductsMonitor and confirm production operations conforming to specifications or requirementsLine ClearanceCritical Process Parameter Line Set UpManagement of StaffManage QC work schedules; accountable for QC team's work hoursResponsible for allocating QC personnel to the production linePerform staff performance evaluationResponsible for the training of the QC personnel, the discipline and morale of the staff.Perform other duties and projects as assigned.Job QualificationsBachelor's degree in Applied Sciences or Engineering (e.g., Biology, Chemistry, Physics, or a related field).At least 5 years of experience in Quality Management, QA, or QC.Proven expertise in Quality Management.Familiarity with Quality Systems, including GMP and GLP, in an FDA-regulated industry.Strong critical thinking and problem-solving skills, with the ability to identify and resolve issues promptly, analyze information effectively, and develop alternative solutions.Excellent interpersonal and communication skills.Capable of managing and developing staff.Collaborative team player.Self-motivated and proactive.Job BenefitsHealth Insurance:
Comprehensive medical, dental, and vision coverageRetirement Plans:
401(k) plan, often with company matchingLife Insurance:
Coverage for employees in the event of death or disabilityPaid Time Off (PTO):
Vacation days, sick leave, and personal daysHolidays:
Paid company holidays and floating holidaysProfessional Development:
Training programs and opportunities for career advancementPerformance Bonuses:
Annual merit increase and/or bonus based on individual performanceCompany Events:
Team-building activities, social events, and company outingsEmployee Assistance Programs (EAPs):
Confidential counseling and support services for personal and professional issues.EEOIntercos Group is committed to creating a diverse and inclusive workplace where everyone is valued and respected. We believe that a wide range of perspectives and experiences enhances our innovation and success. We are an Equal Opportunity Employer and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or any other legally protected status. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to any of these characteristics. We are dedicated to providing a work environment that is free from discrimination and harassment and promotes equal opportunity for all.