Location: Ashland City, TN
Quality Assurance (QA) jobs involve the systematic monitoring and evaluation of the various aspects of a project, service, or facility to ensure that standards of quality are being met. The primary goal is to identify defects and issues before the product reaches the customer, thereby ensuring customer satisfaction and maintaining the reputation of an organization. QA roles often require attention to detail, strong problem-solving skills, and a good understanding of industry-specific regulations and standards. These jobs can vary widely, from software testing to food safety inspection, but they universally function as a critical checkpoint in the production and delivery process of goods or services.
Quality Assurance (QA) Jobs encompass roles focused on ensuring that products or services meet established standards of quality, reliability, and performance. These positions typically involve identifying defects, designing test procedures, conducting tests, and making improvements. Key characteristics of QA jobs include attention to detail, a strong understanding of quality metrics, the ability to analyze data, and problem-solving skills. Individuals in QA roles work closely with development teams and are critical in maintaining customer satisfaction by preventing errors and enhancing the user experience.
and conducting experiments. They must report imperfections and make recommendations for improvements. The quality control technician will inspect incoming panels, in process press, milling and finished products. The tech will check for specified milling dimensions, durability, check records of operators to ensure compliance to manufacturing process.
The technician is required to learn the thirty-three different procedures standards. These procedures of production verification are imperative to ensure the product quality. Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Identify imperfections using mechanical
or electronic equipment Perform routine tests to determine that products meet required standards Conduct analysis of samples, compile data, and interpret the results using computer software Report inconsistencies, malfunctions, or variations from prototype Write up explanation of flaws Evaluate procedures Recommend new or revised methods for production efficiency Prepare samples for testing Competencies Must work responsibly and independently with little supervision Written communication skills Technical capacity Q uality Control Technician Pay & Benefits Competitive Hourly Pay - $16.26 ($17.26 with shift premium) Shift Premium - $1.00 per hour Overtime Hours and Pay Full Plan of Benefits 3rd
Shift: S-Th 7:30pm - 6:00am with occasional overtime on Friday $500 sign-on bonus after 90 days - $200 after 60 days; Remaining $300 after 90 days Please refer to the " Full Job Description" button below to review our physical demands form prior to applying to this position.
Federal and NY State Labor Laws /images/New York Federal Combo English. pdf
industry-competitive pay and benefits. Our facility in Pulaski, TN currently has openings for a Quality Auditor on the midnight shift (11:00pm to 7:30am). The Quality Auditor performs a wide variety of quality functions that require a thorough knowledge of automotive manufacturing procedures and practices.
Supports manufacturing, quality engineering and in-coming suppliers to ensure adherence to customer requirements. Works directly with in-coming suppliers, monitors and reports performance. The ideal candidate for this position is team-focused with excellent communication skills and would be responsible for the following: Inspect parts for defects, ensure quality standards are achieved
Gauge and test component parts required Reads processing information such as logs, product processing sheets, and specification sheets, to verify that records adhere to quality assurance specifications.
Record variable and attribute data Writes and submits audit report/paperwork to appropriate personnel Other duties and responsibilities as required Education and Qualifications Required: High School diploma or GED Above-average Microsoft Office skills Experience in automotive manufacturing Experience in plastic injection molding an asset
skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Summary This is a leadership role that is responsible for a team of Quality Operations Specialist, which will require providing oversight of quality documentation and operations in adherence to c GMPs and SOP regulations.
QOps Supervisors will represent Quality at cross-functional meetings, providing Quality input and decision making in Quality events and deviations. They will provide training to group and departments when needed. Coordinate review of manufacturing Batch Production Records (BPRs) and associated supporting documentation including logbooks,
Quality Control (QC) testing reports, environmental monitoring reports, etc. Serve as owner of assigned nonconformances, CAPA, change controls, or other quality system documents and collaborate to drive completion Create, review and approve documents in Master Control Serve as QOps representative for client project teams as assigned by management Coordinate performance of key QOps functions by team members, including line clearances, general manufacturing support, product shipment, raw material receipt and release, etc.
Participate in departmental and cross-functional continuous improvement efforts Train and mentor assigned QOps Specialists and Leads Promote a safety mindset through daily
actions and communication with team members Manage risk and escalate issues to QOps management in a timely manner Communicate professionally, effectively, , and efficiently with all clients, internal and external Job Qualifications Bachelors degree in a life science or related field preferred Minimum of 5 year GMP related experience in biomedical/medical or related industry or a combination of 5 years of education and related work experience required Experience with GMP regulatory requirements The pay range for this position is $74,700 - 83,500 annually.
Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
Compensation Data About Biologics Testing Solutions With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and medical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products.
Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety backssment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges.
Our client base includes global medical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe.
We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, or national origin, veteran or disability status. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to xyz X@.
This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit.
