Quality Specialist Salary at Secova Inc BETA

The QC Specialist organizes and runs the routine analysis of the Quality Control Department. This role is crucial in ensuring the Quality Control Department meets the efficiency goals while satisfying customers. This individual is responsible for conducting inspection and testing procedures during manufacturing processes and receiving inspection processes to ensure the products comply with requirements. Technical Expertise: KEYENCE INSPECTION Requirements ASQ certification and at least 5 years of medical device experience Ability to ensure organization and prioritization in order to meet production goals and deadlines Excellent written and verbal communication skills and attention to detail Ability to problem solve and maintain critical thinking Sound understanding of the concepts and principle of inspection techniques and methods. Knowledge and understanding of geometric dimensioning and tolerance. Ability to interpret engineering drawings and handle various types of measuring instrum

Work for a Central New Jersey (Somerset County) area company that produces electro-mechanical power connection products. Quality Specialist (Quality Assurance): Summary: The Quality Specialist is responsible for supporting quality improvement initiatives, reducing defects, and ensuring processes meet company standards. This role involves conducting defect analysis, implementing corrective actions, and working with production teams to improve quality and efficiency. Key Responsibilities: * Quality Improvement Projects: o Lead and support initiatives focused on reducing production defects, waste, scraps, and rework. o Work closely with production teams to implement corrective and preventive actions (CAPA). o Track and report progress on assigned quality improvement projects. * Defect Analysis & Troubleshooting: o Investigate recurring quality issues and assist in root cause analysis. o Support data collection and trend analysis on defects and process inefficiencies. o Recommend and help

Our CPG client is currently seeking a Quality Specialist for their facility near Hoboken, New Jersey. ***Only candidates with FOOD/CPG experience will be considered*** This job will have the following responsibilities: Maintain, organize and schedule samples for testing, conduct appropriate evaluations and summarize results. Perform various physical and chemical tests of finished products while recording accurate data in a timely manner. Ensure that testing equipment is accurately calibrated and functioning properly. Monitor weights, codes, labeling, and perform sensory evaluations and record data. Other duties include auditing distribution centers and manufacturing sites to ensure compliance to regulatory regulations, GFSI auditing schemes, HACCP and best food industry practices. Qualifications & Requirements: Five years experience within the food quality assurance industry. Knowledge of codes of federal regulations 101 through 123. Experience with HACCP, Food Safety Plans and Foreign

Quality Specialist Pennington, New Jersey **Job Description:** One of the keys to driving Responsible Growth is being a great place to work for our teammates around the world. Were devoted to being a diverse and inclusive workplace for everyone. We hire individuals with a broad range of backgrounds and experiences and invest heavily in our teammates and their families by offering competitive benefits to support their physical, emotional, and financial well-being. Bank of America believes both in the importance of working together and offering flexibility to our employees. We use a multi-faceted approach for flexibility, depending on the various roles in our organization. Working at Bank of America will give you a great career with opportunities to learn, grow and make an impact, along with the power to make a difference. Join us! **Job Description:** This job is responsible for testing and delivering software to accomplish business outcomes. Key responsibilities of the job include ensu

Requisition ID: 282855 Relocation Authorized: None Telework Type: Full-Time Telework Work Location: Bethlehem, PA Hourly Range: $45.00 - $50.00/hour (Determined by function, education, experience, and qualifications of the applicant.) Extraordinary teams building inspiring projects: Since 1898, we have helped customers complete more than 25,000 projects in 160 countries on all seven continents that have created jobs, grown economies, improved the resiliency of the world's infrastructure, increased access to energy, resources, and vital services, and made the world a safer, cleaner place. Differentiated by the quality of our people and our relentless drive to deliver the most successful outcomes, we align our capabilities to our customers' objectives to create a lasting positive impact. We serve the Infrastructure; Nuclear, Security & Environmental; Energy; Mining & Metals, and the Manufacturing and Technology markets. Our services span from initial planning and investment, through star

Under the direction and oversight of the PV Quality and Compliance Associate Director, this role will: •Perform reviews of individual case safety report compliance monitoring outputs to ensure high quality and compliant reporting in accordance with PV regulations and business partner agreements. •Assist with the development and implementation of processes used to monitor the compliance of individual case safety reports •Participate in compliance monitoring special projects as needed to ensure data quality . Education and Experience: •Bachelor's degree/Master's degree in life science with minimum 4-5 years of relevant experience within investigation, deviation in the Pharmacovigilance( PV) space. •Strong analytical skills and quality focus •Knowledge of Pharmacovigilance principles, systems, and requirements in addition to Pharmacovigilance regulations •Experience with Pharmacovigilance investigations or deviation management Software expertise: •Office 365 applications •Safety database(

The Quality Specialist should be an experienced Construction or Engineering Professional who is able to review our projects to verify they meet all necessary requirements before they are turned over to the client. The Quality Specialist will be responsible for performing scheduled audits and random spot inspections of the work in progress, the final/finished product and project quality document control to verify these items have been completed in compliance with all applicable codes, standards, plans and specifications, and meets customer requirements and expectations. The Quality Specialist should be thorough and observant with an eye for detail. The Quality Specialist must fully understand the requirements for the product (project), and/or be willing to perform self-exploration of project documents, codes, standards and other research to learn the requirements, and have a sense of responsibility towards our reputation in the industry. The primary goal of the Quality Specialist is to

Data and Quality Specialist Staten Island, NY (http://maps.google.com/maps?q=56+Bay+Street+Staten+Island+NY+USA+10301) Behavioral Health Job Type Full-time Description Title:Data and Quality Specialist, Harm Reduction Department:Behavioral Health Reports To:Associate Vice President, Harm Reduction Location:56 Bay Street, Staten Island, NY 10301 Position Status:Full-Time FLSA Status:Non-Exempt Pay Rate: The pay range for this role is generally$41,600-46,600 annuallycommensurate with relevant experience and qualifications and in alignment with internal equity. Additionally, we offer an excellent benefits package that includes generous paid time off (4 weeks of vacation plus paid holidays, personal, and sick time), medical, dental, vision, supplemental benefits including employer provided basic life insurance and employee assistance programs, tuition reimbursement and fitness reimbursement after 1 year of employment, a retirement plan that includes employer matching, and more! Community H