1. As necessary, acts as a key member of projects to improve clinical and non clinical areas. Partners with internal and external departmental leadership in meeting goals and objectives. Interacts with Managers, Staff, Department Heads, Clinical Service Coordinators, Vice Presidents, and Chiefs of respective departments in relation to projects. 2. Acts as an active partic

Quality Manager LOCATION Danbury, CT, US, 06810 REQ ID 46686 If you are a current employee click here to apply. SEE designs and delivers packaging solutions that protect essential goods transported worldwide, preserve food, enable e commerce and digital connectivity, and help create a global supply chain that is touchless, safer, less wasteful, and more resilient. SEE str

Responsible for the verification of product characteristics and associated manufacturing documentation and other quality records, utilizing a range of inspection techniques and methods including, but not limited to visual, mechanicals, automated, contact and non contact. This responsibility will be discharged under the authority delegated by quality. Job Responsibilities

Apply Now > Save Job Job Saved Accurately and efficiently assembles/tests a variety of moderately complex products to achieve customer quality and on time delivery schedules. May perform lockwiring, first stage subassembly, and final detailing functions. Works on products that contain mechanical components, single hydraulic systems, and multiple part numbers. Actively con

Accurately and efficiently assembles/tests a variety of moderate to semi complex products to achieve customer quality and on time delivery schedules. May perform lockwiring and final detailing functions. Works on products that contain mostly mechanical and some electrical components, single and some dual hydraulic systems, and multiple part families. Actively contributes

Accurately and efficiently assembles/tests a variety of moderate to semi complex products to achieve customer quality and on time delivery schedules. May perform lockwiring and final detailing functions. Works on products that contain mostly mechanical and some electrical components, single and some dual hydraulic systems, and multiple part families. Actively contributes

Lead quality functions for assigned programs from proposal through shipment to customer while complying with customer requirements and achieving EBAD cost and delivery expectations. Determine root cause and implement corrective actions for customer complaints and product defects. Host external quality audits and participate in internal quality audits. Participates in new

Compliance Specialist II Job Locations US CT Southington | US United States Requisition ID 2024 16866 Category Compliance Position Type Regular Full Time Overview The ideal candidate will have 5 or more years' progressive experience as a product/filing analyst handling core commercial lines business. Candidate will have expertise with ISO, NCCI, SERFF, AAIS and with vario

The Lead, QA Documentation Specialist is responsible for overseeing the daily quality assurance process, ensuring successful product releases, and managing the timely issuance, reconciliation, review and release of production records, including the creation of Certificates of Analysis (COAs) and Certificates of Compliance (COCs). ESSENTIAL FUNCTIONS AND BASIC DUTIES Maint

The purpose of the Quality Systems Specialist is to perpetuate Enterprise wide Quality and Regulatory compliance and continuous improvement through assisting with the implementation and maintenance of robust quality systems and processes and engaging with related projects. This includes but is not limited to Change Control Management, Enterprise GXP Training and Qualifica

Inspector II 1st Shift Location Location US CT Bloomfield Requisition ID 2024 8285 Category Quality Assurance/Control Segment Kaman Aerospace Shift Shift 1 # of Openings 1 Posted Date 2 hours ago (5/16/2024 11 01 AM) Overview Kamatics, a division of Kaman, has an exciting opportunity for an Inspector to join our Bloomfield, CT team on 1st shift. This position will perform

Investigates by observing, sampling, testing, and reporting in areas such as o Hazardous materials o Food protection o Lead poisoning prevention o Swimming pool and public bathing area sanitation o Insect and rodent control o School and institutional sanitation o Public health nuisance control ...and other factors of the environment that cause or have deleterious effect u

Inspects buildings and dwellings for possible sources of lead poisoning. Conducts investigations, following established protocols, of home environments of children exhibiting the symptoms of blood lead poisoning. Performs inspections using special instruments to identify surfaces containing lead paint. Collects samples of paint, dust, water, and soil from dwellings and de

Under the direction of the Director Quality, the Manager Facility Quality is responsible for ensuring the compliance of the quality systems, manufacturing processes and associated records for adherence to Nestle Health Science. Standard Operating Procedures (SOP's) and Good Manufacturing Practices (cGMP's) that are in effect within their manufacturing site, assuring the q

Ensures that the packaging line runs productively following all Packaging Operations SOPs and cGMPs Completes appropriate paperwork Monitors product from the line for accuracy and ensures proper packing procedure is utilized for shipment Complies with company policies and procedures and maintains regular work attendance Follows safety rules, SOP's and cGMP guidelines Main