2nd Shift Manufacturing Operations Lead

Quva

Bloomsbury (NJ)

On-site

USD 57,000 - 78,000

Full time

5 days ago
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Benefits offered by this job

Set, full-time schedule
Health, dental and vision benefits
401k retirement program with company%2
22 paid days off + 8 holidays per year
Career advancement opportunities

Job summary

Quva in Bloomsbury, NJ is seeking a Supervisor, Manufacturing Operations (ILP) to lead ILP labeling and packaging activities, coordinating staff and equipment to meet production schedules while upholding cGMP and quality standards.

The role is on the 2nd shift, Wednesday through Saturday 3:30PM–1:30AM, a safety-sensitive position with potential drug testing. We value training, adherence, and continuous improvement in a growing company.

Qualifications

  • High school diploma or GED required.
  • 2–3 years in cGMP/FDA regulated industry.
  • 1 year of supervisory/management experience.
  • Certifications in-house qualification programs completed.
  • Experience training personnel on aseptic techniques.

Responsibilities

  • Supervise ILP operations and label printing activities.
  • Schedule ILP to align with production and demand.
  • Prepare reports and analyze metrics for improvement.
  • Participate in safety meetings and investigate incidents.
  • Ensure delivery performance and adherence to plans.
  • Manage frontline leadership on daily tasks.
  • Drive Quality Management System assignments.
  • Review batch records and logs for compliance.
  • Develop training programs and ensure delivery.
  • Initiate schedule changes and coordinate repairs.

Skills

cGMP / FDA regulations
Supervisory experience
Aseptic technique training
Gowning techniques
Safety and lifting up to 50 lbs

Education

High school diploma or GED
Bachelor’s Degree in Life Science

Tools

Tracking software

Job description

Quva in Bloomsbury, NJ is seeking a Supervisor, Manufacturing Operations (ILP) to lead ILP labeling and packaging activities, coordinating staff and equipment to meet production schedules while upholding cGMP and quality standards.

The role is on the 2nd shift, Wednesday through Saturday 3:30PM–1:30AM, a safety-sensitive position with potential drug testing. We value training, adherence, and continuous improvement in a growing company.

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