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Supervisor, Production - Weekend

Job in Newark, Essex County, New Jersey, 07175, USA
Listing for: 6AM City, LLC
Full Time position
Listed on 2026-06-07
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Operations Manager
Salary/Wage Range or Industry Benchmark: 81650 USD Yearly USD 81650.00 YEAR
Job Description & How to Apply Below
Position: Supervisor, Production - Weekend (Friday - Sunday)

Overview

The Supervisor, Packaging Operations is responsible for the skin packaging production activities for CMC (Collagen Manufacturing Center) to ensure the safety, efficacy, and quality of our medical devices. The role includes assigning and monitoring weekend (Friday through Sunday) first‑shift activities, partnering with support departments, and ensuring compliance with ISO 7 and ISO 5 Clean Rooms, GMP, Quality Systems Regulations, SOPs, and Health and Safety requirements.

The position is on‑site and requires a 12‑hour weekend first shift.

Supervision

Reports to the Senior Manager, Manufacturing and directly supervises weekend first‑shift manufacturing cleanroom operators and lead operators.

Responsibilities
  • Ensure a safe working environment for all employees.
  • Facilitate teamwork, cooperation, and lean culture development to enhance employee engagement and customer satisfaction.
  • Meet established cost, quality, and delivery commitments within FDA device regulations and ISO standards.
  • Directly coordinate and evaluate the manufacturing area, ensuring SOPs are followed.
  • Provide daily coaching and development for direct reports.
  • Review production reports, address operational, manufacturing, and maintenance issues to minimize costs and delays while maintaining quality and regulatory compliance.
  • Train employees on company, government procedures, and regulations.
  • Collaborate with Facilities, Maintenance, Engineering, Quality, Warehouse, and Planning teams for seamless shift flow.
  • Maintain gowning qualification for ISO 5 and ISO 7 Clean Rooms.
  • Oversee hiring, training, performance management, and complaint resolution.
  • Perform other related duties and special projects as assigned.
Qualifications
  • Bachelor's degree or higher in Science, Engineering, or related fields.
  • At least 3 years of relevant leadership experience in a GMP‑regulated industry.
  • Knowledge of NCs, CAPAs, and FDA regulations including ISO 9001 and ISO 13485.
  • Strong written and verbal communication skills.
  • Strong leadership skills with a team‑focused approach.
  • Ability to gown into ISO 7 and ISO 5 Clean Rooms.
  • Experience in batch manufacturing.
  • Proficiency with Microsoft Office;
    Oracle R12/Agile preferred.
  • Understanding of Lean and Six Sigma a plus.
Salary and Benefits

Salary range: $81,650.00 – $ USD. The compensation may include bonus, commission, equity or other variable elements. Eligible employees may participate in company‑sponsored programs such as medical, dental, vision, life insurance, short‑ and long‑term disability, business accident insurance, group legal insurance, and a 401(k) savings plan.

Equal Opportunity Employer

Integra Life Sciences is an equal opportunity employer and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

Legal Notice

All volunteers and employees must comply with the Americans with Disabilities Act and Receive accommodations as appropriate. The company is governed by applicable U.S. laws and federal regulations. If you have questions about your rights under the law, please consult the U.S. Equal Employment Opportunity Commission resources.

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