Quality assurance specialist jobs in Meriden, CT - 133 jobs

Quality Control Supervisor Our client, a leading biopharmaceutical company, is seeking an experienced Quality Control Supervisor to join their team. This role is responsible for overseeing QC operations in a GMP-regulated environment, ensuring compliance with regulatory standards and internal procedures. Key Responsibilities: Supervise and mentor QC analysts; provide technical guidance and support. Ensure compliance with cGMP, USP, and 21 CFR Parts 210 & 211. Review and approve analytical data, investigations, and CAPAs. Troubleshoot analytical instruments (HPLC, GC, PSD) and support method validation and transfers. Manage testing schedules for raw materials, finished products, stability, and validation samples. Qualifications: BS in a scientific discipline with 5+ years of experience or MS with 3+ years. Hands-on experience with HPLC and Empower software. Strong knowledge of cGMP, USP, and ICH guidelines. Supervisory experience required. This is an excellent opportunity to join a growing organization and make an impact, please apply in directly for more information!

360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services and operations, the company caters to its globally positioned clients by providing dynamic feasible IT solutions. 360 IT Professionals work along with its clients to deliver high-performance results, based exclusively on the one of a kind requirement. Our services are vast and we produce software and web products. We specialize in Mobile development, i.e. iPhone and Android apps. We use Objective C and Swift programming languages to create native applications for iPhone, whereas we use Android Code to develop native applications for Android devices. To create applications that work on cross-platforms, we use a number of frameworks such as Titanium, PhoneGap and JQuery mobile. Furthermore, we build web products and offer services such as web designing, layouts, responsive designing, graphic designing, web application development using frameworks based on model view controller architecture and content management system. Our services also extend to the domain of Cloud Computing, where we provide Salesforce CRM to effectively manage one's business and ease out all the operations by giving an easy platform. Apart from this, we also provide IT Staffing services that can help your organization to a great extent as you can hire highly skilled personnel's through us. We make sure that we deliver performance driven products that are optimally developed as per your organization's needs. Take a shot at us for your IT requirements and experience a radical change. Job Description Responsibilities: · Provide necessary definition, development and deployment of software quality assurance strategy and roadmap. · Develop and maintain current and comprehensive test plans for Navigators applications. · Act as Subject Matter Expert on the technical aspects, and tools related to testing end to end processes. · Lead and develop the execution of manual and automation test cases and scripts. · Lead and perform various types of testing including functional, regression, performance, user acceptance, etc. · Identify, document and track quality issues through to completion. · Responsible for maintaining up-to-date test plans. · Supervise quality assurance team who may be both internal and external resources and who may be geographically dispersed to ensure the delivery of the QA department goals and objectives · Works with project managers to develop project schedules and resource allocation models for QA related projects and other activities such as software deployment in production environments. · Responsible embedding for QA as part of the SDLC · Meet target deployment schedules. · Measure and evaluate product and QA team performance; recommend improvements. · Identify risks and manage contingencies. · Gather and communicate testing results. · Work with Internal Audit to test and evaluate the design and operating effectiveness of internal controls. Requirements: · Bachelor's Degree or equivalent experience · 7+ years of software testing experience · 4+ years of team leadership · Thorough understanding of formalized QA process and concepts · Proven track record of delivering projects on time and within budget · Experience with Software Development Life Cycle (SDLC) · Strong analytical and problem solving abilities · Additional Information Thanks & Regards Vikas Kumar vikas.kumar(@)360itpro.com

As a Warehouse Quality Assurance Administrator, you'll monitor and evaluate inventory control processes and procedures. You'll lend your talents to verifying inventory accuracy in Best Buy distribution centers, delivery pads and service depots. Using established procedures, you'll also audit receiving, shipping and warehousing operational processes. To help us improve our practices, you'll report your audit results to the relevant supply chain leaders. What you'll do * Assist in monitoring inventory discrepancies, diagnosing problems, developing recommendations and requesting inventory adjustments * Advise warehouse staff and managers regarding concerns, potential issues, opportunities and operational recommendations * Communicate with corporate teams regarding inventory discrepancies and progress towards resolution * Provide training assistance related to procedural processes, systems knowledge and inventory management to warehouse employees * Help maintain clean work areas by removing empty pallets, sweeping and cleaning up boxes and other debris Preferred qualifications * Able to lift up to 75 pounds with or without reasonable accommodation * Able to stand, sit and walk for long periods of time * Proper training and certification on necessary equipment * Experience with inventory, warehousing or general office responsibilities What's in it for you We're committed to helping our people thrive at work and at home. We offer generous benefits that address your total well-being and provide support as you need it, especially key moments in your life. Our benefits include: * Competitive pay * Generous employee discount * Financial savings and retirement resources * Support for your physical and mental well-being About us As part of the Best Buy team, you'll help us fulfill our purpose to enrich lives through technology. We bring that to life every day by humanizing and personalizing tech solutions for every stage of life - in our stores, online and in customers' homes. Our culture is built on deeply supporting and valuing our amazing employees who make it all possible. We're committed to being a great place to work, where you can unlock unique career possibilities. Above all, we aim to provide a place where you can bring your full, authentic self to work now and into the future. Tomorrow works here. Best Buy is an equal opportunity employer. Application deadline: Minimum of 5 days from the posting date. You can find that date above the job title at the top of the page. Auto Req. ID1012968BR Location Number 002319 DPAD-NEW HAVEN Address 8 Northrup Industrial Park Rd$18.77 - $28.79 /hr Pay Range $18.77 - $28.79 /hr

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you. Director, Clinical Quality Assurance The Director, Clinical Quality Assurance position is responsible for design, delivery and execution of the North America (NA) Clinical Quality Assurance (CQA) strategy including audit and inspection management and oversight of the Quality management system. This role is responsible for Good Clinical Practice (GCP) oversight, and for assuring the compliance of projects, products and programs with Eisai's Standard Operating Procedures (SOPs), Policies, and all applicable worldwide regulations and guidelines (e.g. US, EU Directives, US FDA, PMDA, ICH). Essential Functions * Independently conduct audits * Review and oversee results of CQA audits of study sites, clinical vendors, clinical documents, and internal process audits * Facilitate Sponsor health authority inspections of global clinical facilities and study sites * Continuously drive innovation through active search, evaluation, acquisition, and implementation of high-impact new technologies/ procedures across clinical quality programs * Direct skill-building interventions for CQA staff through cross-functional/ external partnerships to reskill/ upskill and adapt the workforce to evolving technologies. * May be responsible for direct people management including goal setting, performance management, development, and engagement. Requirements * Bachelor's degree in an associated functional discipline (advanced degree preferred) with minimum 12 years in clinical research/ operations/ data management or related area. * 5+ years of experience in GCP auditing. * Substantial experience in inspection management. * Substantial experience with US, EU, and international regulatory standards and guidelines for the conduct of clinical trials. * Demonstrated ability to operate and influence decision-making processes * Effective communication skills * Successful track record of supervising employees and managing cross-cultural differences * Technical and administrative capabilities to independently carry out routine, complex and for-cause audits * Knowledge of data integrity controls and systems quality for clinical area * Strong analytical skills and report writing skills * Experience with GxP systems including computer system validation and associated regulations, recommended. * Ability to Travel (approximately 20%) * Candidates near Eisai's NJ/PA location will be preferred. For candidates near an Eisai location, Remote Work Arrangement will consist of 2-4 days in office (Nutley/Exton) per month and 1-2 audits quarterly; remote audits, are held in Nutley. CQA is also expected to be present in Nutley for any inspections or critical inspection mgmt. activities. Eisai Salary Transparency Language: The base salary range for the Director, Clinical Quality Assurance is from :195,000-256,000 Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan. Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills. Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit *********************************************** Certain other benefits may be available for this position, please discuss any questions with your recruiter. Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans. Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information: Right To Work E-Verify Participation

Description & Requirements Maximus is currently hiring for a Quality Assurance and Training Manager to support our Kansas Eligibility Operations team. This is a remote opportunity. The Quality Assurance and Training Manager will will oversee quality assurance programs, manage remote training teams, and ensure compliance with contractual and regulatory standards. In this role, the Quality Assurance and Training Manager will design and implement training strategies, monitor performance, and leverage standardized quality tools to enhance service delivery and to meet client's needs. *This role is contingent upon contract award* Why joining Maximus? - • Competitive Compensation - Quarterly bonuses based on performance included! - • Comprehensive Insurance Coverage - Choose from various plans, including Medical, Dental, Vision, Prescription, and partially funded HSA. Additionally, enjoy Life insurance benefits and discounts on Auto, Home, Renter's, and Pet insurance. - • Future Planning - Prepare for retirement with our 401K Retirement Savings plan and Company Matching. - • Unlimited Time Off Package - Enjoy UTO, Holidays, and sick leave, - • Holistic Wellness Support - Access resources for physical, emotional, and financial wellness through our Employee Assistance Program (EAP). - • Recognition Platform - Acknowledge and appreciate outstanding employee contributions. - • Tuition Reimbursement - Invest in your ongoing education and development. - • Employee Perks and Discounts - Additional benefits and discounts exclusively for employees. - • Maximus Wellness Program and Resources - Access a range of wellness programs and resources tailored to your needs. - • Professional Development Opportunities- Participate in training programs, workshops, and conferences. Essential Duties and Responsibilities: - Design, develop and implement training curriculum and supporting materials. - Develop training schedules based on the evaluation of the need for new staff. - Develop and deliver training through input and communication with the client and leadership. - Ensure that Client Service Reps are provided with updated knowledge required for the project, which includes management of changes to scope and direction. - Communicate operating policies and procedures and ensure compliance with contractual agreement. - Arrange staff training on a regular and ongoing basis regarding telephone protocols and project information obtained through quality assurance monitoring. - Manage quality operations including planning, implementing, monitoring, and reporting functions. - Manage internal and external customer expectations related to quality management, and effectively communicate corporate quality standards across the project. - Support and improve the Quality Program and provide the leadership and direction to enhance accepted standards of quality practices, continuous improvement, and ethical considerations. - Aggregate and analyze quality data and identify opportunities for improvement in product and service quality, and the design and implementation of key business and quality processes. - Maintain responsibility for developing, implementing, and writing procedures, work instructions and flow-charts for quality management activities and monitoring compliance with contractual agreements. Minimum Requirements - Bachelor's degree in relevant field of study and 5+ years of relevant professional experience required, or equivalent combination of education and experience. - Must be willing and able to travel up to 25% of the time as business need dictates. - Lean Six Sigma experience with a minimum of Yellow Belt Certification required. - Experience managing direct reports remotely required, as well as multiple training sessions virtually. - Experience with designing, implementing and reporting customer satisfaction surveys required. - Experience with standardized quality tools required. - Experience with call and voice monitoring platforms required. - Experience with a large-scale telephony system required. - Experience with Client Relationship Management (CRM) platforms required. - Experience with contract compliance and quality platforms required. - Experience with statistical processes required. - Premium contact center billing experience required. - Financial experience with Oracle preferred. - Medicaid program knowledge and experience highly preferred. Home Office Requirements: - Internet speed of 25mbps or higher required (you can test this by going to ******************* - Connectivity to the internet via either Wi-Fi or Category 5 or 6 ethernet patch cable to the home router. - Must currently and permanently reside in the Continental US. EEO Statement Maximus is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information and other legally protected characteristics. Pay Transparency Maximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment. Annual salary is just one component of Maximus's total compensation package. Other rewards may include short- and long-term incentives as well as program-specific awards. Additionally, Maximus provides a variety of benefits to employees, including health insurance coverage, life and disability insurance, a retirement savings plan, paid holidays and paid time off. Compensation ranges may differ based on contract value but will be commensurate with job duties and relevant work experience. An applicant's salary history will not be used in determining compensation. Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances. Accommodations Maximus provides reasonable accommodations to individuals requiring assistance during any phase of the employment process due to a disability, medical condition, or physical or mental impairment. If you require assistance at any stage of the employment process-including accessing job postings, completing assessments, or participating in interviews,-please contact People Operations at **************************. Minimum Salary $ 100,000.00 Maximum Salary $ 112,400.00

Responsibilities: Actively participate in overall day-to-day operational leadership and decision making as the subject matter expert for all project quality management functions Provide ongoing and regular quality control related technical input for construction planning, interpretation of design, development of efficient construction methods and quality control processes for execution of work Manage and schedule all required quality testing, inspection, and documentation including all third-party quality control related services Manage the quality control process required per contract documents, specifications, drawings, and engineering calculations for work activities Provide overall leadership to ensure work is constructed in compliance and work quality is accurately documented through clear and traceable record keeping and reporting Qualifications: Bachelors degree in engineering 10 years of experience in any of the combinations of: field inspection experience, construction experience relevant to the type of work and the scope of the project, and/or previous experience as a QC professional NETTCP Quality Assurance Technologist certified Working Place: Torrington, Connecticut, United States Company : Ogind- Sept 26 Fair National fair

Reno Machine Company and its subsidiary TM Industries, located at 134 Commerce Street in East Berlin, CT, are looking for skilled candidates. Reno Machine Company and TM Industries are CNC-based manufacturing facilities that focus on large-format machining for aerospace, defense, power generation and research development projects. As a quality manager, you will devise and safeguard quality standards while overseeing processes that directly affect the products' overall integrity. You will create and implement quality policies and regulations, analyze data, inspect, and test products and document the resolved issues. This position is excellent for anyone who is thorough, observant, has an eye for detail, and has a positive team-oriented attitude. Duties Knowledgeable in performing first piece, in process, final inspection, calibration of measuring instruments and CMM operation. Supervise and guide inspectors, technicians, and other staff. Works with staff and customers, legal and safety authorities to improve quality, efficiency, and profitability. Monitor all operations that affect quality. Setting requirements for raw material or intermediate products for supplies and monitoring their compliance. Inspect final product to make sure it has been built in compliance with legal standards to meet customers' expectations. Assure the reliability and consistency of production. Use online portal or customer database. Interpret and apply AS/ISO standards. Manage the Quality department and its employees. Interface with both internal and external customers to address any quality issues. Maintain highest standards while meeting the company cost & scheduling requirements. Continual evaluation of policies & procedures to develop improvements to the system. Control & maintain the calibration system. Perform & maintain internal/external audits. Perform other duties as assigned by the director of quality. Experience 5 years minimum experience in a quality management function. 1-3 years supervisory experience. Thorough knowledge of methodologies of quality assurance and standards. Experience with AS 9100 required. Must pass eye exam to Jaegar 1 with color. Outstanding communication skills. Computer fundamentals required. Previous DSQR background required. Excellent written and oral communication skills. Flexible to work long hours as required to meet deadlines. Job Type: Full-time Benefits: 401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Vision insurance

Cardinal Health PET Manufacturing Services is responsible for manufacturing PET radiopharmaceuticals to enhance patient treatment through improved disease diagnosis, staging, and monitoring. The primary work environment consists of a manufacturing pharmacy which must be kept clean, orderly, properly lighted and maintained in optimum operating condition. Employees handle radioactive materials and are exposed to very low amounts of radiation that are deemed safe by current standards. The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory group. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate. **What Quality Assurance contributes to Cardinal Health** + Quality Assurance is responsible for developing and implementing a compliant and cost-effective quality system that assures products and services are reliable, safe and effective + Demonstrates knowledge of quality systems and approaches. + Demonstrates an understanding of the relevant regulations, standards and operating procedures. + Demonstrates ability to perform investigations / root cause analysis and develop corrective actions. + Demonstrates an understanding of the requirements and has the ability to perform gap assessments to those requirements. + Demonstrates an understanding of quality concepts such as: cost of quality, analytical metrics and / or statistics, trending, quality planning, validation, CAPA and problem solving. + Works cross-functionally and has the ability to interpret the requirements as well as educate and influence others on those requirements. **Schedule** : 40 hours per week. This is a night position. Typically Monday through Friday 1:30 am to 9:30 am. Candidate must be flexible to work different shifts or schedules based on business need. Candidate must be comfortable staying until work is completed each business day. Work hours may be subject to change. **Accountabilities** + Handles CGMP documentation review related to product release, facilities and equipment, material controls, laboratory controls, packaging and labeling, and production & process controls. + Establishes and reports metrics related products and processes as deemed necessary by the Regional Quality Manager RQM. + Ensures the site manufactures products to meet the requirements of 21 CFR 212 (CGMP) + Handles and ensures quality of documentation (control, retention, and archival) to support CGMP activities + Engages and collaborates with operations department to drive quality system and CGMP requirements + Performs product release activities per CGMP requirements + Reports quality system issues to the RQM and others as necessary. This includes timely escalation of discrepancies upon identification. **Qualifications** + Bachelor's degree in related field (science), or equivalent work experience (Microbiology, Chemistry, Biology, Physics), preferred + 2+ years of experience in related science field preferred + 1-2 years of experience in Quality Assurance and/or regulated environment highly preferred - cGMP + Pharmaceutical or medical device experience a plus + Effective written and verbal English communication skills + ISO experience a plus + Ability to lift up to 75 lbs **What is expected of you and others at this level** + Applies working knowledge in the application of concepts, principles, and technical capabilities to perform varied tasks + Works on projects of moderate scope and complexity + Identifies possible solutions to a variety of technical problems and takes actions to resolve + Applies judgment within defined parameters + Receives general guidance may receive more detailed instruction on new projects + Work reviewed for sound reasoning and accuracy + Ability to manage several tasks at the same time; Ability to focus on tasks ; Ability to evaluate operating conditions + Ability to exercise sound judgment Personal Protective Equipment **Anticipated salary range:** $76,700.00-$98,550.00 **Bonus eligible:** No **Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close:** 2/12/2026 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

**About PSI** We are PSI Services. We power world leading tests. Delivered with trusted science and the very best test taker experience. PSI supports test-takers on their journey to pursuing dreams and gaining certifications that are important to them. They believe that their dreams are worth working for; that their dreams are worth the effort. And we believe that too. This is our core purpose, to empower people to achieve their dreams. We do this by being the best provider of workforce solutions, which foster both technology and science to deliver the best solutions for our test takers. We are searching for top talent to join our PSI team and help grow our products and services. We have a creative, supportive and inclusive culture where we empower people in their careers to be their authentic self and make the most of their great talent. At PSI, we are committed to helping people meet their potential and we believe that promoting diversity, equity and inclusion is critical to our success. That's why you'll find these ideals are intrinsic to our company culture and applied throughout the employee lifecycle. Learn more about what we do at: ************************* **About the Role** + The Quality Assurance Analyst is responsible for ensuring quality of technology that PSI provides to its customers. The person in this role works closely with the Software Engineering teams to understand what has been developed. They also work closely with the solutions and product teams to ensure business requirements are being tested. This role is critical to the successful delivery of PSI's services and the quality of its products. This role adds significant value to the operation of PSI's Credentialing business, as this work is crucial for supporting our customers first-hand with a quality service and maintaining our people-focused brand. + This is a full-time permanent role, with flexible hours around core office availability Monday to Friday. The role can be performed remotely, working across time zones, with occasional travel required for meetings, events and workshops. **Role Responsibilities** + Responsible for managing and executing end-to-end testing for key technology platforms and be accountable for test projects. + Use principles, guidelines, and best practices as defined, and document testing plans. + Gather and present testing metrics and testing activities for the projects to key stakeholders. + Closely work with product teams to understand requirements and other performance SLAs. + Reviewing and analysing feature requirements exit criteria and design test scenarios. + Perform various types of testing, including but not limited to the following: Functional, Regression, integration, backend data validation, usability, end to end system testing, API testing, performance/stress testing and ensure bug-free applications go to production. + Writing, executing, and managing the manual test cases. + Identify, validate, communicate, and track to closure defects and risks to the development team(s) and clearly communicate testing status and QA roadblocks to the QA manager and Product Managers. Interacts closely with members of cross-functional project team including Development, PMs, and Client Services. + Provide the UAT support for business users as well as client. + Reporting defects accurately and managing to successful resolution via Jira. + Maintaining and creating product knowledge documentation. + Investigate and attempt to diagnose customer support reported defects. + Participate in sprint planning, scrum, and backlog grooming ceremonies. + Researching and embrace new techniques and technology to improve testing + Strong SQL skills to validate data from multiple sources like Files, XMLs, Databases. **Knowledge, Skills and Experience Requirements** + 3 years' experience in progressively responsible information technology. + Proven experience and knowledge of QA methods, standards and processes, e.g. Agile / SDLC. + Excellent numerical skills and understanding of data analysis/statistical methods. + Familiarity with the software development lifecycle and with automation testing technologies. + Experience with version management and ticketing systems, e.g. SVN, Jira. + Experience with RDBMS and SQL, ISTQB principles, testing and debugging in multiple browsers/OS, and experience with API testing tools such as Post-Man or Soup UI. + Experience with accessibility testing is huge plus. + Experience with QA automation tools, test automation frameworks, writing and executing the automation scripts with Selenium WebDriver in JAVA or C# is preferable but not essential. **Benefits & Culture** At PSI, our culture is to be transparent and fair. That's why all of our roles have been benchmarked at a competitive rate against the local market they are based in. To be transparent all of our adverts now include the salary so you can see if we align with your expectations when looking for your next role. In addition to a competitive salary, we offer a comprehensive benefits package and supportive culture when you join us. This includes: + 401k/Pension/Retirement Plan - with country specific employer % + Enhanced PTO/Annual Leave + Medical insurance - country specific + Dental, Vision, Life and Short-Term Disability for US + Flexible Spending Accounts - for the US + Medical Cashback plan covering vision, dental and income protection for UK + Employee Assistance Programme + Commitment and understanding of work/life balance + Dedicated DE&I group that drive core people initiatives + A culture of embracing wellness, including regular global initiatives + Access to supportive and professional mechanisms to help you plan for your future + Volunteer Day and a culture of giving back to our community and industry through volunteering opportunities Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (**************************** notice from the Department of Labor.

Sonsoft , Inc. is a USA based corporation duly organized under the laws of the Commonwealth of Georgia. Sonsoft Inc. is growing at a steady pace specializing in the fields of Software Development, Software Consultancy and Information Technology Enabled Services. Job Description Minimum of at least 2 years of QA experience Knowledge: Expertise on testing Technology for Digital programs that include Omni-channel access as well as customer experience apart from regular functional testing. Substantial exposure to healthcare domain and specific business and working knowledge of US Healthcare system, regulations etc. Understanding of one or more Estimation methodologies, Knowledge of Quality processes. Skills: Analytical abilities, Strong Technical Skills, Good communication skills, ability to work in a multiple / diverse stakeholders environment, People coordination Strong automation expertise, with hands on experience in Java - Junit test framework in Eclipse IDE. Should have experience in developing automation for web, Mobile (hybrid and Native apps) and service virtualization testing (Includes web Services and APIs) Experience with Web Automation tools such as Selenium, Mobile automation tools such as Appium/Perfecto & service automation using Soap UI. Preferred Minimum 2 years of core Healthcare domain expertise within the Testing experience Minimum 2 years of hands on experience with automation testing, with ability to design and maintain scalable frameworks for Web, service and mobile automation. Knowledge of integration with DevOps orchestration tool such as Jenkins, BDD parsers such as Cucumber, XMLs for communication within interfaces. Understanding of the SOAP and Rest protocols for Services Exposure to IBM rational set of tools such as RFT, RTC, uDeploy, RIT & RTW Exposure to US healthcare requirements like HCR, Medicare/Medicaid, Compliance, HIPPA, HealthCare Exchange (HIX) Expertise in Functional testing, analysis and reporting skills Expertise on Software Testing Life Cycle Methodologies like waterfall, Agile Delivery Exposure to various testing estimation models Very good knowledge of Defect Life Cycle Management Good verbal, written communication skills and analytical abilities, SQL Awareness Understanding of technical architecture like client server, n-Tier, service oriented • Experience and desire to work in a Global delivery environment Your responsibilities will include, but not limited to : Strong exposure & experience in executing projects in an agile mode. Closely work with various stakeholders (such as BA, Dev, Product owner), to prioritize and define acceptance criteria for user stories in form of System behavior. Support the creation of functional and non-functional requirements documents by creating specifications based on client SME inputs, reviewing demos of existing systems and through discussions with supervisor. Support preparation of the Requirements Traceability Matrix using Testing Requirements Engineering process and tools. Define a suitable estimation model and provide estimations for planned tasks. For projects executed in an agile mode, need to provide estimates in term of User story points. Should Define and Plan tasks for all identified stories in a sprint. Should have ability to develop and deploy automation to all feasible repeated manual tasks, to bring in efficiencies. Excellent communication skills and should be able to clearly outline risks, mitigation plans and any other dependencies or assumptions. Provide support for Test design. Create test cases for complex modules based on the defined test strategy for the assigned module. For the assigned module, implement guidance given on test data, perform set-up activities, prepare scripts (SQL, etc.) to create test data as required and populate test data in a timely manner. Execute test cases as planned for the assigned modules with special focus on key modules using knowledge of test execution process for both functional and non-functional type of testing. Perform specific activities for the given module as per the "Go-live" implementation plan with guidance from supervisor. Should have experience in developing Automated test cases (using Behavior driven development and Test driven development methodology) and integrating it with a DevOps pipeline for Continuous validation and process automation Participate in and prepare content for KT sessions, capture understanding of assigned module, and take on shadow support. Participate in onsite-offshore interactions as required, prepare and submit daily status reports to supervisor and provide timely updates for project trackers on the module assigned. Document and share own learnings from the project, seek information and leverage knowledge from other modules. Provide inputs for the Requirements Traceability Matrix (RTM). Qualifications Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education. At least 2 years of experience with Information Technology Additional Information ** U.S. Citizens and those who are authorized to work independently in the United States are encouraged to apply. We are unable to sponsor at this time. Note:- 1.This is a Full-Time & Permanent job opportunity for you. 2.Only US Citizen Green Card Holder, GC-EAD, H4-EAD & L2-EAD can apply. 3.No OPT-EAD, H1B & TN candidates please. 4.Please mention your Visa Status in your email or resume.

The Quality Assurance (QA) Specialist conducts qualitative and quantitative testing of products and raw materials throughout the entire production process, ensuring products and packaging meets standards. As a QA Specialist, you are responsible for setting up and participating in experiments and research as directed by the QA Manager. QA Specialists may be cross-trained and asked to support other departments occasionally to meet business needs. This is a full time position at $18 per hour in our Rocky Hill (CTPharma) facility. Shift time is 10am-6:30pm. Essential Duties and Responsibilities * Perform quality inspections, auditing against cGMP and SQF criteria and confirming product quality standards are being met. * Monitor and ensure traceability of plant and product movement throughout the facility. * Perform periodic review of procedures, forms, logs, and master batch records. * Assist in customer complaints and product investigations-helping to assess risk, identify root cause, and provide solutions. * Inspect packaged orders to ensure correct content and quantities as deemed necessary. * Ensure the consistency and efficiency of products through quality control testing and procedures. * Collect samples as needed for quality testing. * Regularly clean and sterilize equipment and workspace. * Maintain strict inventory record of raw materials, chemicals, waste, and equipment. * Manage, document, and dispose lab waste. * Maintain Material Safety Data Sheets (MSDS) for all chemicals and products. * Follow laboratory safety protocols. * Monitor and maintain quality control measures in accordance with state and local laws. * Perform quality inspections, auditing against cGMP and SQF criteria and confirming product quality standards are being met. * Monitor and ensure traceability of plant and product movement throughout the facility. * Perform periodic review of procedures, forms, logs, and master batch records. * Assist in customer complaints and product investigations-helping to assess risk, identify root cause, and provide solutions. * Inspect packaged orders to ensure correct content and quantities as deemed necessary. * Ensure the consistency and efficiency of products through quality control testing and procedures. * Collect samples as needed for quality testing. * Regularly clean and sterilize equipment and workspace. * Maintain strict inventory record of raw materials, chemicals, waste, and equipment. * Manage, document, and dispose lab waste. * Maintain Material Safety Data Sheets (MSDS) for all chemicals and products. * Follow laboratory safety protocols. * Monitor and maintain quality control measures in accordance with state and local laws. * Adhere to company policies and Standard Operating Procedures (SOP). * Maintain a clean and safe working environment within the facility and production areas. * Immediately inform QA Manager of any system or equipment discrepancies. * Ensure all products are of high quality and visually aesthetic, reporting concerns to management for remediation. * Perform other duties as assigned by management. Minimum Qualifications * High school diploma, GED, or equivalent required. * 1 year of QA experience in a laboratory setting or 2 years of manufacturing assembly line experience required. * Must have a positive attitude and work well with others in a team environment. * Willing to learn about, operate, and maintain facility equipment in a safe manner. * Able to understand proper and safe handling of hazardous materials. * Must have effective time management and multitasking skills. * Must have strong computer skills. * Ability to safely climb, squat, bend, twist, kneel and stand for at least 8 hours per day, and lift up to 25 pounds. * Must be authorized to work in the United States. * Must be 21 years of age or older and able to successfully register with the state's cannabis commission as an agent. * Must comply with all laws, regulations, and policies associated with the industry. Preferred Qualifications * Associate degree or equivalent preferred. Physical and Mental Demands While performing the duties of this job, the employee is frequently required to remain in a stationary position, move and/or position oneself, communicate, operate and/or prepare, place, position objects, tools, or controls. The employee must occasionally move packages weighing up to 25 lb. Able to stand for 90% of the time. Comfortable with heights, occasionally ascends/descends a ladder to service the lights, filters, trellis netting and ceiling fans up to 25ft. Comfortable working atop and traversing scaffolding, when required. Comfortable with changing environment temperatures and humidity. Exposure to pollen, dust, dander, and other nature elements. Specific vision abilities required by this job include close observation and the ability to adjust focus. The mental and physical requirements described here are representative of those that must be met by an individual, with or without reasonable accommodation, to successfully perform the essential functions of this position. Working Environment Work is performed in a warehouse environment. The employee is occasionally exposed to moving mechanical parts and risk of electrical shock. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position. We are proud to be an equal opportunity employer. We place priority in an environment of inclusion, diversity and social justice and are committed to securing a better, brighter way forward for our employees, our markets, and our communities.

Job DescriptionDescription: 2nd Shift, 3:30 pm- 12:00 am, Monday through Friday SCA Pharmaceuticals is a dynamic, rapidly growing company consisting of passionate individuals who believe in our mission of providing high-quality medications that are critical in saving and sustaining human life. SCA Pharma is an FDA 503B outsourcing facility providing customized medications for hospitals and healthcare facilities across the United States. We do this through unyielding quality, safety, and integrity, our commitment to accountability and ownership, teamwork and creating better solutions by simplifying the complex. Summary: The Quality Assurance (QA) Inspection Associate will report to QA Management and is a core member of the site Quality Assurance team. The QA Inspection Associate will serve as the Quality point of contact for Manufacturing Quality Assurance (MQA) with inspection. The site is focused on continuous improvement of all work processes and practices; therefore, in addition to routine Quality Assurance inspection duties, QA Associates may be asked to carry out additional work functions to support site continuous improvement activities. This is a first and second shift role required to perform the product AQL inspection process and oversight of the ILP operation lines Processes. Essential functions/Responsibilities: Perform manual product visual inspection, AQL (Acceptable Quality Limit) of injectable product to ensure the entire product (lot) has met thresholds established. Monitor inspection operations to ensure that they meet production standards. Observe and provide real-time quality oversight and support for manufacturing on the floor. Provides quality support for initiating events within the inspection process. Provides training and advice to inspection staff for them to perform their desired functions. Support continuous improvement and operational excellence initiatives. Other duties as assigned. Requirements: Qualifications & Experience: High school diploma or equivalent 1+ years of relevant experience working in the pharmaceutical industry. Knowledge, Skills, and Abilities: Knowledge of Microsoft Office Suite (Word, Excel, Outlook) Ability to understand, interpret and perform all activities in compliance with SCA safety standards and standard operating procedures. Have strong written and verbal communication skills. Have strong attention to detail. Ability to keep large batches of products organized. Ability to safely operate packaging equipment. Ability to stand and/or sit for long hours at a time. Good visual acuity and manual dexterity. Must be able to work independently or in a team. Must be able to regularly move and manipulate objects up to 30 lbs. Ability to sit or stand for prolonged periods of time. Ability to wear all required PPE. SCA Pharma is an equal opportunity employer (Minorities/Females/Disabled/Veterans). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state, or local law.

Job DescriptionDescription: The Part-Time Quality Associate supports the Quality Department at the Wallingford Distribution Center. This role receives and manages components and retain samples, conducts sampling and inspections, and executes release decisions for third-party co-manufactured finished goods, packaging components, and received retains. The position maintains retain sample storage and logs, pulls retains for complaint investigations, reviews manufacturing jobs performed at Wallingford, and manages local document control. The associate also coordinates closely with the Middletown manufacturing facility (Production, Shipping/Receiving, and Quality) and maintains compliance with cGMP/GDP requirements under 21 CFR Part 111. MAJOR RESPONSIBILITIES: · Compliance with Standard Operating Procedures, GMPs and related systems that ensure company compliance and applicable regulations · Receive, log, and stage incoming components and retain samples in accordance with SOPs. · Maintain retain sample storage conditions, inventory, and chain-of-custody; pull retains to support complaint investigations. · Perform sampling and visual/physical inspections of incoming materials and finished goods per approved methods. · Review documentation (e.g., COAs, specifications, receiving records) and determine release/hold status for third-party co-manufactured finished goods, packaging components, and received retains. · Perform quality approval and documentation review for manufacturing jobs executed at the Wallingford Distribution Center (e.g., kitting, rework, relabeling). · Verify completion, legibility, and GDP compliance of all associated records; ensure line clearance and reconciliation requirements are met. · Review and maintain quality documentation and logbooks for the Wallingford team. · Execute local document control activities (issuing/archiving controlled documents and forms, processing requests from Middletown, ensuring current versions are in use). · Coordinate with Middletown Production, Shipping/Receiving, and the main Quality team on releases, holds, investigations, and material movements. · Escalate deviations, complaints, and potential quality issues promptly per SOP. · Adhere to cGMP and GDP practices and maintain required training to ensure compliance with 21 CFR Part 111. · Support internal/external audits and maintain inspection-ready work areas and records. · Follow site safety, housekeeping (5S), and PPE requirements. · Destruction of rejected/expired materials following company SOP's and guidelines · Operate forklift and other power equipment as needed · Must prepare and complete required documentation · Perform additional duties as assigned KNOWLEDGE/SKILLS/EXPERIENCE: · Must have a high school diploma or general education degree (GED); Associates degree strongly preferred in Food Science, Nutrition, Biology, or Chemistry · Experience in · Ability to read, write, and communicate about work instructions and safety information written in English · Understanding of basic mathematical concepts · Ability to analyze and interpret technical information · Computer skills including MS office and material control programs · Advanced organizational skills · Ability to follow and interpret instructions whether written or spoken · Ability to work well in a team · Strong communication and interpersonal skills · Punctual and reliable in work attendance PHYSICAL REQUIREMENTS: · Must be able to lift up to 50 pounds on a regular basis · Operation of forklift and other power equipment · Works near moving mechanical parts · Vision requirements: Requires distance vision, color visions, peripheral vision, depth perception and ability to focus · Must wear PPE and GMP appropriate for the position: non-slip footwear (boots), hair net, beard net (if applicable), face masks, nitrile food-grade gloves Blueroot Health™ is an Equal Opportunity Employer. Employment opportunities at Blueroot Health™ are based upon one's qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, religion, sex, national origin, age veteran status, disability, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment. Requirements:

The Quality Representative's primary functions are to assure manufacturing validations and operations meet the quality system requirements and assisting quality engineers with customer complaint and quality issues. This position will provide guidance and input on quality issues and validation activities. This position will audit compliance to the quality policy and procedures. The incumbent will participate in continuous improvement, validation, and customer complaint activities in support of business goals. This position reports directly to a Quality Engineer. - Perform various testing procedures and simple statistical analysis. - Perform complete inspection of product according to applicable specifications. - Responsible for internal documentation updates in SAP when applicable. - Record the results of inspections and audit findings. - Possess knowledge of Quality System Regulations - Possess knowledge of control charting defect trends in product quality. - Train associates to inspect product per the appropriate specifications, and utilize all gauges/ equipment pertaining to Quality Assurance testing. - Must perform duties and maintain knowledge to conduct inspections and tasks among all manufacturing/molding departments. - Perform other miscellaneous duties as appropriately directed by Quality Management. **Job Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a **maker of possible** with us. The Quality Manufacturing Representative's primary functions are to assure manufacturing operations meet the quality system requirements and assisting quality engineers with quality issues. This position will provide guidance and input on quality issues and validation activities. This position will audit compliance to the quality policy and procedures. The incumbent will participate in continuous improvement, validation, and customer complaint activities in support of business goals. This position reports directly to a Quality Engineer. **Essential Functions:** + Ensure manufacturing associates are properly trained in documented inspection techniques and methods. + Trend quality metrics and communicate to appropriate individuals. + Investigate specific problem areas in manufacturing and report to management on findings and suggest corrective actions. + Initiate and/or respond to correction and preventive actions as required. Document quality system failures and improvement activities. + Apply and interpret ANSI/ASQ Z1.4 and other sampling plans for predicting percent defective and lot acceptance criteria. + Conduct routine product and process audits to assure compliance to the quality system. + Audit inspection reports for compliance. + Assist quality engineers with validations, quality issues, data collection, etc. + Maintain a clean and safe work environment. + Hold self-accountable to follow all safety policies & procedures + Work with others (interpersonal skills) + Give and receive feedback + Solve problems and make informed decisions + Plan and organize job tasks + Set priorities and timelines + Break down tasks into their parts + Take initiative (see what needs to be done and then do it) + Work with others (interpersonal skills) + Give and receive feedback + Solve problems and make informed decisions + Plan and organize job tasks + Set priorities and timelines + Break down tasks into their parts + Take initiative (see what needs to be done and then do it) **Duties and Responsibilities:** + Perform various testing procedures and simple statistical analysis. + Perform complete inspection of product according to applicable specifications. + Responsible for internal documentation updates in SAP when applicable. + Record the results of inspections and audit findings. + Possess knowledge of Quality System Regulations + Possess knowledge of control charting defect trends in product quality. + Train associates to inspect product per the appropriate specifications, and utilize all gauges/ equipment pertaining to Quality Assurance testing. + Must perform duties and maintain knowledge to conduct inspections and tasks among all manufacturing/molding departments. + Perform other miscellaneous duties as appropriately directed by Quality Management. **Education:** + High School Diploma or GED At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. **Why Join Us?** A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. \#earlycareer Required Skills Optional Skills . **Primary Work Location** USA CT - Canaan **Additional Locations** **Work Shift** US BD 3rd Shift 10pm-630am (United States of America) Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

SummaryThe Quality Representative's primary functions are to assure manufacturing validations and operations meet the quality system requirements and assisting quality engineers with customer complaint and quality issues. This position will provide guidance and input on quality issues and validation activities. This position will audit compliance to the quality policy and procedures. The incumbent will participate in continuous improvement, validation, and customer complaint activities in support of business goals. This position reports directly to a Quality Engineer. • Perform various testing procedures and simple statistical analysis. • Perform complete inspection of product according to applicable specifications. • Responsible for internal documentation updates in SAP when applicable. • Record the results of inspections and audit findings. • Possess knowledge of Quality System Regulations • Possess knowledge of control charting defect trends in product quality. • Train associates to inspect product per the appropriate specifications, and utilize all gauges/ equipment pertaining to Quality Assurance testing. • Must perform duties and maintain knowledge to conduct inspections and tasks among all manufacturing/molding departments. • Perform other miscellaneous duties as appropriately directed by Quality Management.Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. The Quality Manufacturing Representative's primary functions are to assure manufacturing operations meet the quality system requirements and assisting quality engineers with quality issues. This position will provide guidance and input on quality issues and validation activities. This position will audit compliance to the quality policy and procedures. The incumbent will participate in continuous improvement, validation, and customer complaint activities in support of business goals. This position reports directly to a Quality Engineer. Essential Functions: Ensure manufacturing associates are properly trained in documented inspection techniques and methods. Trend quality metrics and communicate to appropriate individuals. Investigate specific problem areas in manufacturing and report to management on findings and suggest corrective actions. Initiate and/or respond to correction and preventive actions as required. Document quality system failures and improvement activities. Apply and interpret ANSI/ASQ Z1.4 and other sampling plans for predicting percent defective and lot acceptance criteria. Conduct routine product and process audits to assure compliance to the quality system. Audit inspection reports for compliance. Assist quality engineers with validations, quality issues, data collection, etc. Maintain a clean and safe work environment. Hold self-accountable to follow all safety policies & procedures Work with others (interpersonal skills) Give and receive feedback Solve problems and make informed decisions Plan and organize job tasks Set priorities and timelines Break down tasks into their parts Take initiative (see what needs to be done and then do it) Work with others (interpersonal skills) Give and receive feedback Solve problems and make informed decisions Plan and organize job tasks Set priorities and timelines Break down tasks into their parts Take initiative (see what needs to be done and then do it) Duties and Responsibilities: Perform various testing procedures and simple statistical analysis. Perform complete inspection of product according to applicable specifications. Responsible for internal documentation updates in SAP when applicable. Record the results of inspections and audit findings. Possess knowledge of Quality System Regulations Possess knowledge of control charting defect trends in product quality. Train associates to inspect product per the appropriate specifications, and utilize all gauges/ equipment pertaining to Quality Assurance testing. Must perform duties and maintain knowledge to conduct inspections and tasks among all manufacturing/molding departments. Perform other miscellaneous duties as appropriately directed by Quality Management. Education: High School Diploma or GED At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. #earlycareer Required Skills Optional Skills . Primary Work LocationUSA CT - CanaanAdditional LocationsWork ShiftUS BD 3rd Shift 10pm-630am (United States of America)

The Senior Quality Control Technician role in our Bloomfield, CT facility drives improvement in the reliability of CO2 Laser products. The incumbent will be engaging directly with a cross functional team on a wide variety of products to ensure our product and processes meet the dynamic laser manufacturing requirements. Working with a quality mindset team, this role will provide hands on support for the incoming goods, in-process, and final inspection of laser systems to ensure we meet Coherent Quality Standards. Primary Duties & Responsibilities * Inspection manufactured laser systems: * Detail oriented inspection of electronic and mechanical assemblies * Utilize common inspection methods to evaluate critical design requirements * Develop inspection test plans with a cross functional team * Assist in problem solving activities to support identified nonconformities * Evaluation and verification of purchased components * Define and execute incoming material test plans for qualification activities * Document and present inspection results to key stakeholders * Verification of vendor supplied documentation including first article inspections and material certifications * Support of Quality Systems: * Document detailed findings to be used for Continuous Improvement Initiatives * Accomplish root cause analysis and provide corrective actions with follow-up * Ensure practices align with best practices, procedures and inspection techniques * Perform internal product and business system audits * Reliability system maintenance: * Utilize computers for automated data collection and control of instruments * Collaborate with the Quality organization regarding calibration of test instruments * Monitor and troubleshoot long term unmanned tests with engineering support * Assist in developing new methods and protocols for component level testing and measurement * Complete calibration of monitoring and measuring equipment support Education & Experience * High School diploma * A minimum of 4 years of related experience or combination of education and relevant experience * Proficient in the use of automated and manual measuring devices and test equipment * Excellent verbal and written skills in the English language required Skills * Preferred experience with layout inspections and sound Geometric Dimensioning and Tolerancing knowledge * Preferred experience automating inspection test method is preferred * Knowledge of centralizing data for analysis * Experience of test and measurement of electronic and/or optical systems * Continuous improvement mindset - improves products and processes * Well organized and knowledgeable of 6S methodology * Demonstrated problem-solving abilities combined with hands-on experience * Knowledge of electronic component manufacturing * Self-motivated to thoroughly document data and test results Working Conditions * Manufacturing working environment. Some areas under cleanroom protocol. * Minimal to no expected travel * Support of seconds shift operations required * This is an on-site position in our Bloomfield, CT facility. * Shift will be Monday to Friday 11am to 7:30pm Physical Requirements * Must be able to move around manufacturing floor * Must be able to lift a maximum of 30 pounds Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.

As a Warehouse Quality Assurance Administrator, you'll monitor and evaluate inventory control processes and procedures. You'll lend your talents to verifying inventory accuracy in Best Buy distribution centers, delivery pads and service depots. Using established procedures, you'll also audit receiving, shipping and warehousing operational processes. To help us improve our practices, you'll report your audit results to the relevant supply chain leaders. What you'll do Assist in monitoring inventory discrepancies, diagnosing problems, developing recommendations and requesting inventory adjustments Advise warehouse staff and managers regarding concerns, potential issues, opportunities and operational recommendations Communicate with corporate teams regarding inventory discrepancies and progress towards resolution Provide training assistance related to procedural processes, systems knowledge and inventory management to warehouse employees Help maintain clean work areas by removing empty pallets, sweeping and cleaning up boxes and other debris Preferred qualifications Able to lift up to 75 pounds with or without reasonable accommodation Able to stand, sit and walk for long periods of time Proper training and certification on necessary equipment Experience with inventory, warehousing or general office responsibilities What's in it for you We're committed to helping our people thrive at work and at home. We offer generous benefits that address your total well-being and provide support as you need it, especially key moments in your life. Our benefits include: Competitive pay Generous employee discount Financial savings and retirement resources Support for your physical and mental well-being About us As part of the Best Buy team, you'll help us fulfill our purpose to enrich lives through technology. We bring that to life every day by humanizing and personalizing tech solutions for every stage of life - in our stores, online and in customers' homes. Our culture is built on deeply supporting and valuing our amazing employees who make it all possible. We're committed to being a great place to work, where you can unlock unique career possibilities. Above all, we aim to provide a place where you can bring your full, authentic self to work now and into the future. Tomorrow works here.™ Best Buy is an equal opportunity employer. Application deadline: Minimum of 5 days from the posting date. You can find that date above the job title at the top of the page.

Cardinal Health PET Manufacturing Services is responsible for manufacturing PET radiopharmaceuticals to enhance patient treatment through improved disease diagnosis, staging, and monitoring. The primary work environment consists of a manufacturing pharmacy which must be kept clean, orderly, properly lighted and maintained in optimum operating condition. Employees handle radioactive materials and are exposed to very low amounts of radiation that are deemed safe by current standards. The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory group. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate. What Quality Assurance contributes to Cardinal Health Quality Assurance is responsible for developing and implementing a compliant and cost-effective quality system that assures products and services are reliable, safe and effective Demonstrates knowledge of quality systems and approaches. Demonstrates an understanding of the relevant regulations, standards and operating procedures. Demonstrates ability to perform investigations / root cause analysis and develop corrective actions. Demonstrates an understanding of the requirements and has the ability to perform gap assessments to those requirements. Demonstrates an understanding of quality concepts such as: cost of quality, analytical metrics and / or statistics, trending, quality planning, validation, CAPA and problem solving. Works cross-functionally and has the ability to interpret the requirements as well as educate and influence others on those requirements. Schedule: 40 hours per week. This is a night position. Typically Monday through Friday 1:30 am to 9:30 am. Candidate must be flexible to work different shifts or schedules based on business need. Candidate must be comfortable staying until work is completed each business day. Work hours may be subject to change. Accountabilities Handles CGMP documentation review related to product release, facilities and equipment, material controls, laboratory controls, packaging and labeling, and production & process controls. Establishes and reports metrics related products and processes as deemed necessary by the Regional Quality Manager RQM. Ensures the site manufactures products to meet the requirements of 21 CFR 212 (CGMP) Handles and ensures quality of documentation (control, retention, and archival) to support CGMP activities Engages and collaborates with operations department to drive quality system and CGMP requirements Performs product release activities per CGMP requirements Reports quality system issues to the RQM and others as necessary. This includes timely escalation of discrepancies upon identification. Qualifications Bachelor's degree in related field (science), or equivalent work experience (Microbiology, Chemistry, Biology, Physics), preferred 2+ years of experience in related science field preferred 1-2 years of experience in Quality Assurance and/or regulated environment highly preferred - cGMP Pharmaceutical or medical device experience a plus Effective written and verbal English communication skills ISO experience a plus Ability to lift up to 75 lbs What is expected of you and others at this level Applies working knowledge in the application of concepts, principles, and technical capabilities to perform varied tasks Works on projects of moderate scope and complexity Identifies possible solutions to a variety of technical problems and takes actions to resolve Applies judgment within defined parameters Receives general guidance may receive more detailed instruction on new projects Work reviewed for sound reasoning and accuracy Ability to manage several tasks at the same time; Ability to focus on tasks ; Ability to evaluate operating conditions Ability to exercise sound judgment Personal Protective Equipment Anticipated salary range: $76,700.00-$98,550.00 Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. Medical, dental and vision coverage Paid time off plan Health savings account (HSA) 401k savings plan Access to wages before pay day with my FlexPay Flexible spending accounts (FSAs) Short- and long-term disability coverage Work-Life resources Paid parental leave Healthy lifestyle programs Application window anticipated to close: 2/12/2026 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here

The Senior Quality Control Technician role in our Bloomfield, CT facility drives improvement in the reliability of CO2 Laser products. The incumbent will be engaging directly with a cross functional team on a wide variety of products to ensure our product and processes meet the dynamic laser manufacturing requirements. Working with a quality mindset team, this role will provide hands on support for the incoming goods, in-process, and final inspection of laser systems to ensure we meet Coherent Quality Standards. Primary Duties & Responsibilities Inspection manufactured laser systems: Detail oriented inspection of electronic and mechanical assemblies Utilize common inspection methods to evaluate critical design requirements Develop inspection test plans with a cross functional team Assist in problem solving activities to support identified nonconformities Evaluation and verification of purchased components Define and execute incoming material test plans for qualification activities Document and present inspection results to key stakeholders Verification of vendor supplied documentation including first article inspections and material certifications Support of Quality Systems: Document detailed findings to be used for Continuous Improvement Initiatives Accomplish root cause analysis and provide corrective actions with follow-up Ensure practices align with best practices, procedures and inspection techniques Perform internal product and business system audits Reliability system maintenance: Utilize computers for automated data collection and control of instruments Collaborate with the Quality organization regarding calibration of test instruments Monitor and troubleshoot long term unmanned tests with engineering support Assist in developing new methods and protocols for component level testing and measurement Complete calibration of monitoring and measuring equipment support Education & Experience High School diploma A minimum of 4 years of related experience or combination of education and relevant experience Proficient in the use of automated and manual measuring devices and test equipment Excellent verbal and written skills in the English language required Skills Preferred experience with layout inspections and sound Geometric Dimensioning and Tolerancing knowledge Preferred experience automating inspection test method is preferred Knowledge of centralizing data for analysis Experience of test and measurement of electronic and/or optical systems Continuous improvement mindset - improves products and processes Well organized and knowledgeable of 6S methodology Demonstrated problem-solving abilities combined with hands-on experience Knowledge of electronic component manufacturing Self-motivated to thoroughly document data and test results Working Conditions Manufacturing working environment. Some areas under cleanroom protocol. Minimal to no expected travel Support of seconds shift operations required This is an on-site position in our Bloomfield, CT facility. Shift will be Monday to Friday 11am to 7:30pm Physical Requirements Must be able to move around manufacturing floor Must be able to lift a maximum of 30 pounds Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .