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Compounder - Cosmetics & Skincare

Job in Totowa, Passaic County, New Jersey, 07512, USA
Listing for: Englewood Lab, Inc.
Full Time position
Listed on 2026-01-17
Job specializations:
  • Manufacturing / Production
    Manufacturing Production, Quality Engineering
Job Description & How to Apply Below

Compo under

Reports to:

Manager, Manufacturing

Department:
Operations

Responsibility Summary

The Compo under will operate, clean, sanitize, inspect, set-up, disassemble, scales, kettles, mills, extruders, ovens and other associate equipment. The compo under will also handle, measure, add, mix, heat, cool, package, label raw materials, bases, bulks, leads, and other material, and train others as directed.

Responsibilities
  • Safety – Take full responsibility for your personal health and safety by:
    • Following all safety related SOP’s, signs, directions, etc. to safeguard against any incidents or unsafe conditions.
    • Performing all designated safety checks and inspections and taking appropriate actions to ensure safe operation.
    • Wearing all required Personal Protective Equipment (PPE) all the time.
    • Ensuring all safety guards, interlocks and protective devices are in place and operational.
    • Reporting all incidents, near misses and safety concerns immediately.
    • Maintain a neat and tidy work area at all times.
  • Quality – Take full responsibility for the Quality of our product by:
    • Understanding and following all cGMP requirements.
    • Following all quality related SOP’s, signs, directions, etc. to safeguard against any defects, product contamination or material/component mix up.
    • Performing all designated/assigned quality checks, inspections and basic testing and taking appropriate actions to insure conformance to EWL and Customer standards.
    • Wearing all required Personal Protective Equipment (PPE) all the time to prevent product contamination.
    • Ensuring all quality checking devices are in place and operational.
    • Completing all required documents, checklists and forms in a timely, accurate and compliant manner.
    • Following the schedule and reporting any delays that may extend a run beyond its scheduled completion date/time.
    • Monitoring equipment performance and reacting accordingly to any issues that will negatively impact safety, quality and rate.
    • Understanding the schedule and anticipating requirements of next order to minimize time between orders (without sacrificing safety or quality).
  • Cost – Focusing on executing all tasks in line with SOP’s and training to:
    • Avoid errors that might result in quality issues.
    • Minimize scrap and waste.
    • Support performance levels at or above target standards.
Qualifications
  • Intermediate math skills.
  • Trained in cGMP requirements, including batch documentation and sanitization.
  • Quality oriented resolute.
  • Computer skills are required. Will use a tablet and bar code scanner to enter data.
  • Physically capable of manual labor that includes lifting, bending, and reaching.
  • Able to operate large industrial machinery.
  • Able to lift 50 lbs.
  • Able to work 8 hour shifts standing.
  • Reliable and punctual.
  • Speaks, reads, and writes English with clarity, comprehension, and legibility, respectively.
  • Self-motivated with the ability to work responsibly and independently with minimal supervision.
Education
  • High School Diploma/GED or relevant experience.
  • 3-7 years of compounding process experience in cosmetic and or pharmaceutical industries.
Additional Information

This is a full-time contract position. The selected candidate may be employed directly by the company or through a third-party staffing agency. Employment terms, including benefits and compensation, will be determined based on the hiring arrangement.

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