Quality Control Manager at Intercos America
West Nyack, NY 10994, USA -
Full Time


Start Date

Immediate

Expiry Date

12 Nov, 25

Salary

90000.0

Posted On

12 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Critical Thinking, Chemistry, Alternative Solutions, Applied Sciences, Regulated Industry, Communication Skills, Gmp, Physics

Industry

Pharmaceuticals

Description

ABOUT US

Imagine 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 SUMMARY

The 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.

JOB QUALIFICATIONS

  • Bachelor’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 in cosmetic industry
  • 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.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities
  • Quality Control – Product Inspection and Release
  • Testing 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, Texture
  • Product Disposition
  • Determine final disposition of all products
  • Responsible for approving and rejecting all batches
  • Management of Product Hold and Disposition
  • Quality Control Documentation/Samples for Clients
  • Conversion of Product Specifications to Production Line Documentation (checklists, forms)
  • Finished Product Documentation to be issued to Clients, (e.g. COA)
  • Pre-Shipment Samples to Clients
  • Management of Documents and Product Samples Retention Requirements
  • Records /Documentation review and sign off for OTC Products
  • Monitor and Confirm production operations conforming to specifications or requirements
  • Line Clearance
  • Critical Process Parameter Line Set Up
  • Management of Staff
  • Manage QC work schedules; accountable for QC team’s work hours
  • Responsible for allocating QC personnel to the production line
  • Perform staff performance evaluation
  • Responsible for the training of the QC personnel, the discipline and morale of the staff.
  • Perform other duties and projects as assigned.
Loading...