Top 1342 Quality inspection supervisor Jobs in New Jersey

Director of Quality
June Jacobs Labs —Moonachie, NJ
- From $185,000 a year
- Full-time
- Background check
- Bachelor's degree
- In-person
- Health insurance
- Dental insurance
Quick Apply
12d
Supervisor of Operations II
Interstate Waste Services —Secaucus, NJ
- $90,000 - $105,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
Quality Inspection Supervisor
Holtec —Camden, NJ
- $90,000 - $105,000 a year
- Hybrid work
- Mid-level
- 3 years
- High school diploma or GED
- Wellness program
- Commuter assistance
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Quality Control Supervisor
Polymer Concepts Technologies, Inc —Orange, NJ
- $82,000 - $98,000 a year
- Management
- Ability to walk for extended periods
- Mid-level
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Quality Manager - Bridgewater & Fair Lawn, NJ
Thermo Fisher Scientific —Fair Lawn, NJ
- $112,500 - $155,000 a year
- Full-time
- 5 years
- Bachelor's degree
- Mentoring
- Commuter assistance
- Paid parental leave
Quality Control Manager
Englert Inc. —Perth Amboy, NJ
- $100,000 - $115,000 a year
- Full-time
- 5 years
- Engineering
- Analysis skills
- Health insurance
- Dental insurance
Quality Supervisor
Trilogy Warehouse Partners, LLC —Newark, NJ
- $60,000 - $65,000 a year
- Full-time
- Mid-level
- 3 years
- Analysis skills
Quality Supervisor
Astrodyne TDI —Hackettstown, NJ
- $75,000 - $80,000 a year
- Mid-level
- 3 years
- Mentoring
Quick Apply
Quality Specialist II
BioReference Health, LLC —Elmwood Park, NJ
- $81,000 - $91,500 a year
- Bachelor of Science
- Mid-level
- Ability to lift 50 pounds
Community Access Center Supervisor
Occupational Training Center —Burlington, NJ
- $28 an hour
- Full-time
- Clean driving record
- Bachelor of Science
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
Supervisor of Operations II (Overnight)
Interstate Waste Services —Jersey City, NJ
- $90,000 - $105,000 a year
- Overnight shift
- Microsoft Excel
- Microsoft Outlook
- Mid-level
SUPERVISOR, ENVIRONMENTAL SERVICES | FULL-TIME NIGHT SHIFT (25461)
Care Plus Bergen, Inc. —Paramus, NJ
- $50,000 - $70,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Hospital
- Paid holidays
- Health insurance
Quick Apply
Quality Control Inspector
CACI —Florham Park, NJ
- $45,900 - $91,900 a year
- Full-time
- Mid-level
- 3 years
- Continuous improvement
- Health insurance
Supervisor, Quality Assurance
Amneal Pharmaceuticals —Piscataway, NJ
- $90,000 - $105,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- High school diploma or GED
- Health insurance
- 401(k) matching
Senior Inspector Trainer
Kulite Semiconductor Products, Inc. —Leonia, NJ
- $50,000 - $80,000 a year
- Full-time
- High school diploma or GED
- Mentoring
- Manufacturing
- Health insurance
- Dental insurance
Nuclear Medicine Technologist
Cardiac Imaging, Inc. —Bridgewater, NJ
- $60 - $75 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Writing skills
- Health savings account
- AD&D insurance
Quick Apply
Nuclear Medicine Technologist
Cardiac Imaging, Inc. —Newark, NJ
- $60 - $75 an hour
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Writing skills
- Health savings account
- AD&D insurance
Quick Apply
Production Supervisor
Corim Industries —Township of Brick, NJ
- From $25 an hour
- Overtime
- Spanish
- Ability to walk for extended periods
- ERP systems
- Health insurance
- Paid time off
Quick Apply
Maintenance Supervisor
Goldberg Realty Associates —Aberdeen, NJ
- From $57,000 a year
- Full-time
- 5 years
- Mid-level
- Driver's License
- Paid holidays
- Health insurance
Quick Apply
12d
Tractor/Trailer Technician
NATIONAL RETAIL TRANSPORTATION —North Bergen, NJ
- 5 years
- Computer literacy
- Mid-level
Quick Apply

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Director of Quality

June Jacobs Labs -
Moonachie, NJ

Quick Apply

Job Details

Full-time
From $185,000 a year
12 days ago

Benefits

Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Vision insurance
401(k) matching

Qualifications

Biology
Customer communication
Teamwork
Operations management
Experience working in the beauty industry
Manufacturing facility experience
Bachelor's degree
Managing manufacturing teams
General management

Full Job Description

GENERAL ROLE & RESPONSIBILITY

As Director of Quality for a cosmetics/personal care company, you will be accountable to establish, maintain, and improve the plant’s overall Quality Systems while managing the critical functions of Incoming Quality Control, Fill Assembly Specs and Quality Assurance, FG Lab Testing/Release, Document Control, Change Control, Validation, Training, and Vendor/Supplier QA. This role is a partner to all supply chain functions through all phases of manufacturing and production to assure compliance to all appropriate requirements pertaining to Good Manufacturing Practices (GMP.) The position will oversee and customer complaints, non conformances, CAPA, audits, Annual Product Review consistent with FDA/ISO regulations, standards and internal procedures.

The DOQ is expected to develop and implement plans for continuous improvement and more effective and efficient execution of the overall activities of the Quality teams. The interaction with Manufacturing and Product Development areas will be optimized, all leading to the most consistent, high quality, products and processes. A focus on first time right and Cost of Quality is critical. The person is required be a visible and respected leader for Quality and the entire organization. They will participate at the company mid-management level to ensure our best practices include Quality as a key element of our strategic thinking as the business grows.

SKILLS AND COMPETENCIES

Ø Exceptional quality leader who thrives in a fast-paced personal care contract manufacturing environment with capability to oversee all operational aspects of the business’ Quality function.

Ø Demonstrated ability to lead and motivate your team while providing a unifying vision for the entire organization.

Ø Strong knowledge foundation of FDA regulations regarding the manufacture of cosmetics/OTC (FCR 210, 211, ISO).

Ø Proven ability to develop and implement quality management strategy and plans, including resource, systems, processes to support, contribute to, and integrate within, the organization’s annual business plan and long-term growth and continuous improvement strategy.

Ø Proven problem-solving aptitude and multi-tasking skills where prioritization and use of resources is based on business value.

Ø Strong collaboration and communication skills and can interface effectively with all levels of an organization. You have a proven record of accomplishment of critical thinking, flexibility, and innovation.

Ø Thorough knowledge and practical application of cGMP and FDA Compliance rules, regulations and policies

Ø Thorough knowledge of all Good Documentation processes related to QC/QA activities for OTC products

Ø Excellent leadership and hands on execution skills and abilities, including regular floor presence.

Ø Strong motivational skills and effective team building capabilities (inspectors, leads, supervisors, managers)

Ø Ability to effectively prioritize/manage personal time and resources based on business value.

Ø Ability to efficiently and professionally communicate with internal and external customers, vendors, and regulatory bodies.

DETAILED JOB DESCRIPTION

Ø Manages and Improves quality systems that ensure optimum process and product performance.

Ø Leads investigating and implementing corrective/preventative action for customer complaints, nonconforming products, and nonconforming systems.

Ø Develops and manages procedures and work instructions to ensure conformance to specifications, quality systems, safety, and good manufacturing practices.

Ø Maintains a close relationship with Production, Warehouse, Maintenance and R&D to facilitate quality products, and systems designed to achieve quality goals.

Ø Manages the design and implementation of quality-related training programs for QA and Operations personnel in performing required tests, decision-making skills, statistical process control, and other areas as needed. Partners with HR, Operations and R&D to design effective training curriculums to meet best practices manufacturing processes.

Ø Recommends, reviews changes, oversees implementation, and documents any approved design changes that apply to commercial products. Works directly with customers to facilitate specifications, product design, quality systems, information exchange, non-conforming product, variances and investigation.

Ø Sets direction for audits of in-process & finished products, facility housekeeping, sanitation, pest control,

Ø Acts as Project Coordinator and/or Project Leader as assigned for special projects.

Ø Represents the Company in discussions with customers, suppliers, auditors, and regulatory agencies of the county, state, and federal government (USDA, FDA, etc.).

Ø Establishes, prepares and manages necessary department budgets, operating and periodic reports.

Ø Initiates and handles personnel actions such as hires, reviews, promotions, discipline and terminations.

Ø Develops and implements methods, trend analysis metrics, reports and procedures, in order to inform management of status or work activities.

Ø Manage departmental performance against agreed metrics and key performance indicators

Ø Actively contribute to plant policy and strategy.

QUALIFICATIONS/EDUCATION/EXPERIENCE

Ø Bachelor’s degree in life sciences, i.e., biology, chemistry, etc. required. Advance degree preferred.

Ø 10-15 years of relevant experience in Quality is required, at least 3-5 years of that must be in a leadership capacity with managing multiple direct reports

Ø Experience in all areas within Quality Management Systems related to bulk, filling, packaging, testing and release of personal care products. Cosmetic contract manufacturing experience preferred.

Ø Direct experience with regulatory audits, including direct interface with inspectors.

Ø Knowledge and expertise in principles and current Good Manufacturing Practices (GMPs) in a development through commercial application.

Ø Strong knowledge foundation of FDA regulations regarding the manufacture of cosmetics/OTC (210, 211, CFR), including regulatory inspection or support experience is preferred.

Ø Capable to manage multiple priorities and maintain adherence to timelines.

Ø Must be able to build effective working relationships with key business partners, customers, suppliers and peers in order to drive a culture of continuous improvement regarding cost of quality.

Ø Personal Care manufacturing process related experience required with pharma experience considered.

Ø Key Competencies Include: Prioritization based on business value, cross functional team building, Interpersonal and Leadership Skills

Ø Persuasive Written and Oral Communication, Teamwork and Collaboration, and Effective Management of Personnel

Job Type: Full-time

Pay: From $185,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Tuition reimbursement
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

quality inspection supervisor jobs in new jersey

Director of Quality

Supervisor of Operations II

Quality Inspection Supervisor

Quality Control Supervisor

Quality Manager - Bridgewater & Fair Lawn, NJ

Quality Control Manager

Quality Supervisor

Quality Supervisor

Quality Specialist II

Community Access Center Supervisor

Supervisor of Operations II (Overnight)

SUPERVISOR, ENVIRONMENTAL SERVICES | FULL-TIME NIGHT SHIFT (25461)

Quality Control Inspector

Supervisor, Quality Assurance

Senior Inspector Trainer

Nuclear Medicine Technologist

Nuclear Medicine Technologist

Production Supervisor

Maintenance Supervisor

Tractor/Trailer Technician

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