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Jobs at Aspire Pharma

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Packaging and Removal Operator

  • Aspire Pharma

    • On-site
    • Somerset, NJ

Fill and Gel Prep Operator

  • Aspire Pharma

    • On-site
    • Somerset, NJ

Bottling Operator

  • Aspire Pharma

    • On-site
    • Somerset, NJ

Warehouse Associate

  • Aspire Pharma

    • On-site
    • Somerset, NJ

Quality Control Chemist I

  • Aspire Pharma

    • On-site
    • Somerset, NJ

Encapsulation Mechanic / Operator

  • Aspire Pharma

    • On-site
    • Somerset, NJ

Encapsulation Lead Operator

  • Aspire Pharma

    • On-site
    • Somerset, NJ

Maintenance Technician

  • Aspire Pharma

    • On-site
    • Somerset, NJ

QA Inspector I

  • Aspire Pharma

    • On-site
    • Somerset, NJ

1–9 of 9 jobs

Packaging and Removal Operator

  • Aspire Pharma

  • Somerset, NJ 08873
Open in New Tab

On-site

$20 - 25/ HR

Pharma

Manufacturing

  • Posted on:

Job Description

Summary

The Packaging & Removal Operator is responsible for the removal, inspection, polishing, and packaging of finished products in accordance with approved Batch Manufacturing Records (BMRs), Master Batch Records (MBRs), Standard Operating Procedures (SOPs), and current Good Manufacturing Practices (cGMP). This position ensures product quality, compliance, and efficient operation of packaging processes while maintaining a safe and organized work environment.

Responsibilities
  • Perform removal, inspection, polishing, and packaging of finished products in accordance with approved BMRs, MBRs, SOPs, and cGMP requirements.
  • Inspect products for defects and quality attributes, ensuring only acceptable products proceed through the packaging process.
  • Operate packaging and removal equipment safely and efficiently according to established operating procedures and safety guidelines.
  • Complete all required production documentation accurately, including batch records, inspection records, and equipment logs, following Good Documentation Practices (GDP).
  • Maintain compliance with all cGMP requirements, operational procedures, cleaning procedures, safety regulations, and company policies.
  • Perform shift handoffs, communicate production status effectively, and report product quality issues, equipment malfunctions, deviations, or safety concerns to supervision.
  • Maintain equipment and work areas in a clean, organized, and inspection-ready condition, ensuring proper status labeling of equipment and materials at all times.
Qualifications

Educational Qualifications and Experience:

  • High School Diploma or equivalent required.
  • Minimum of 1 year of experience in the pharmaceutical or related manufacturing industry.
  • Knowledge of cGMP regulations and Good Documentation Practices (GDP).
  • Proficient writing, mathematical, and communication skills.
  • Ability to read, understand, and follow SOPs, BMRs, MBRs, and production instructions.
  • Strong attention to detail and commitment to quality.


Physical Requirements:

  • Ability to stand and walk for extended periods.
  • Ability to lift, carry, push, and pull up to 50 pounds.
  • Frequent bending, reaching, twisting, and repetitive hand movements.
  • Ability to visually inspect products for quality defects and packaging compliance.
Education

Degree

High School

Specialization

Diploma
Experience:

1-5 yrs

  • Skills:
  • CGMP
  • Good documentation practices
  • Product Inspection
  • Packaging operations
  • SOP Compliance
  • batch records
  • Attention to detail
  • Job Type:
  • Full-time
  • Shift Type:
  • 8 hour shift
  • Monday to Friday
  • Day shift

Compensation

  • Benefits:
  • 401K
  • 401K Match
  • Medical, Dental, Vision
  • Additional:
  • Base Salary

Job ID:

CGXP_26_31360

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