Quality Control Supervisor NY
6 days ago
Our client is an industry leader offering an awesome work culture with a great team and highly generous benefits package. If you're a leader in the Quality Control / Quality Assurance world within the FDA manufacturing industry , you'll want to apply and interview for this role
Essential Functions and Responsibilities:
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- Directly responsible for management of Quality Inspectors, technicians.
- Assesses priorities and assigns work to reports to assure the project and company priorities are met
- Participates as an active member or as team leader of teams to meet company objectives and assure department responsibilities are completed
- Assist with the development and tracking of department and project budgets
- Develops and implements new Standard Operating Procedures
- Coordinates with team members and outside professionals to assure products, processes, and documentation meet users' needs as well as all applicable FDA and other regulatory agencies' requirements
- Provides input, feedback, and maintenance on department and division procedures and policies
- Follows and directs activities regarding safety and efficacy of products or materials and assesses impact of decisions on patient, health care provider, business, and regulations
- Strong skills in communicating with all levels of technical and manufacturing personnel, and operating management
- Ability to work in a cross-functional team environment, as member or leader of a cross-functional team, as well as ability to independently function in the technical and leadership areas
- Demonstrate effective leadership capability/skills – coaching, personnel development, decision making, and Supervisory discretion
- Analytical and mathematical skills; proficiency in Statistics, Inspection Methods, use of measuring devices, etc.
- Ability to work with in-house and outside manufacturers and suppliers
- Strong ability to analyze and use technical data and resources
- Ability to evaluate/specify requirements for products, product components and assemblies, tooling and fixture
Work Experience Requirements:
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- Minimum 5 years of related experience
- A minimum of 3-5 years of experience should be in a supervisory capacity
- Demonstrated leadership, positive communication and human relation skills
- Demonstrated knowledge of manufacturing and quality systems requirements for medical devices
- Experience in international medical device registration is a plus
Education Requirements:
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- Associates or Bachelor's Degree in Technical or related area preferred
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
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Melville, United States Nesco Resource Full timeOur client is an industry leader offering an awesome work culture with a great team and highly generous benefits package. If you're a leader in the Quality Control / Quality Assurance world within the FDA manufacturing industry , you'll want to apply and interview for this role!Essential Functions and Responsibilities: Directly responsible for management...
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melville, United States Nesco Resource Full timeOur client is an industry leader offering an awesome work culture with a great team and highly generous benefits package. If you're a leader in the Quality Control / Quality Assurance world within the FDA manufacturing industry , you'll want to apply and interview for this role!Essential Functions and Responsibilities: Directly responsible for management...
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