Collecting information
Organizing data
At Addus HealthCare, quality patient care is a top priority and employees are recognized as our greatest asset. Enjoy the experience of working one-on-one with clients and their families to develop a plan of care through the initial assessment process. Promote our positive image in the community as the leading home care provider.. Must be able to travel locally in your own vehicle, and possess a valid driver's license and appropriate automobile insurance coverage. Addus provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Truist Audit Manager is responsible for providing a leadership role in the delivery of high-risk, complex and value-added independent and objective risk-based internal audit assurance and advisory services. The Audit Manager will proactively coach junior team members by providing candid and constructive feedback. Experience in auditing and issue validations reviews (examples of key areas include wealth management, enterprise risk management, credit and information technology).. Possess appropriate professional certification such as Certified Internal Auditor (CIA), Certified Public Accountant (CPA), Certification in Risk Management Assurance (CRMA) and Certified Information Systems Auditor (CISA). Depending on the position and division, this job may also be eligible for Truist's defined benefit pension plan, restricted stock units, and/or a deferred compensation plan.
The Quality Assurance (QA) Manager oversees, implements, and maintains cGMP compliant systems and activities. The GMP QA Manager also monitors Contract Manufacturing Organizations (CMOs) ensuring compliance of the manufacturing, packaging and analytical testing of pharmaceutical dosage forms and drug substances. Leads all external cGMP audits of vendors, including US and International cGMP, GLP, GDP vendor audits, as needed.. Develops with the CMC team and CMOs: drug substances (DSs), drug products (DPs), key raw material and intermediates specifications and stability requirements, master batch records, validated manufacturing processes and analytical methods, and CTM and commercial packaging and labeling.. In October, 2024 Honeywell announced the spin-off of our Advanced Materials business to become a stand-alone publicly traded company, independent of Honeywell.
Meet financial objectives by estimating requirements, preparing annual budgets, and scheduling expenditures. A minimum of an Associate Degree in Engineering Technology or similar field.. Demonstrated knowledge of working on CMM instrument. Knowledge of statistical and SPC methods.. Lean Manufacturing and/or Six Sigma certification
Supervise the cycle count team and coordinate the reporting of the cycle count results. Coordinate cycle count reporting and perform and report on random tests (based on auditor’s design). Report cycle count results on a monthly basis to distribution systems and DC operations management. Coordinate with the safety supervisor for any safety or security concerns. Previous automotive parts warehouse and branch store experience
The Manager of Quality Assurance will focus on establishing quality standards and metrics in support of the new product development pipeline, as well as legacy products.. Provides subject matter expertise in quality engineering such as: risk management and risk assessments, design verification, equipment qualification, process validation, design transfer, configuration management, and change control.. Six Sigma Green Belt preferred. Dog friendly office - feel free to bring your best buddy with you to work!. This ranges from small department-specific teambuilding or informal outings to our annual Fam Jam family carnival that celebrates the people in your life who support you in bringing your best self to work each day.
Full Spectrum Operations LLC (FSO) is a SDVOSB JV between American Communication Solutions LLC, an SBA VetCert verified SDVOSB, and By Light Professional IT Services LLC (By Light). FSO is looking for personnel to support the Network Enterprise Center Picatinny Arsenal New Jersey (NEC PANJ) with classified and unclassified communication systems support. Perform system testing for OSP and ISP Cabling and report test results to the NEC Project Manager and monthly reports. Read and interpret test results for OSP and ISP cabling systems upon request. Assist in arranging meetings to conduct inspections, reviews, and surveys pertaining to communications construction with Department of Public Works (DPW), United States Army Corp. of Engineers (AcoE) and Picatinny Arsenal.
The person in this position must be an expert on our client's guidelines and play a large role in quality assurance, video content review, and entry-level project management. Savvy with your laptop and smartphone; you enjoy learning new systems and programs.. Travel to different states to conduct undercover evaluations for our clients.. Fill out reports after conducting the undercover evaluations.. This is a full-time hourly job, working remotely at home, except when traveling
The Quality Assurance Manager will work closely with the plant's management team and lead QC Laboratory to provide accurate and timely analytical support to plant production teams, minimize the environmental impact, and ensure Divisional Quality system (QA) requirements are being met at the plant site. Coach the plant management team and train plant personnel on quality systems (QA) and best practices with the goal of preventing quality deficiencies and promoting continuous Improvement. Ensure QC Lab provides accurate and timely analytical support to plant production teams.. Assist Divisional Quality Manager in maintaining risk-based QMS programs and procedures, ensuring divisional compliance and training needs are met. 5+ years experience as a lab technician or chemist in a chemical industry with extensive knowledge of HPLC & GC instrumentation
We are seeking an experienced Senior Quality Assurance Manager to lead the Quality and Food Safety programs at the Bakersfield manufacturing facility.. The ideal candidate will bring deep expertise in ESL (Extended Shelf Life) and aseptic operations, a strong quality manufacturing and regulatory background, and the leadership capabilities to drive a culture of quality across cross-functional teams.. Acts as the QA/Food safety manager when QA director is not present. Implements proactive quality improvement programs and statistical process controls (SPC). Executes all Special Projects as assigned by the Quality Director
Our client is seeking a Quality Assurance (QA) Supervisor who lives and breathes quality excellence. Oversee meticulous quality inspections for PCBs, electronic assemblies, and precision sheet metal parts. Lead investigations into non-conformances-drive root cause analysis and deploy smart CAPA solutions. 5+ years of QA/QC experience in electronics manufacturing, including 2+ years in a leadership role. Inspection of Precision sheet metal components and assemblies to detailed drawings or files
Ongoing quality assurance and surveillance of aircraft fleet maintenance and airworthiness for both part 91 and air carrier operations. Current and valid FAA Mechanic Certificate with Airframe and Powerplant Ratings.. Eight years' experience as a licensed maintainer of modern civil turbojet aircraft.. Aviation maintenance or quality assurance management experience is preferred.. Experience with FAA SAS, DRS, and VDRP are preferred
Bachelor's degree in Food Science, Microbiology, Chemistry, Engineering or a related field. Familiarity with continuous improvement methodologies such as Lean, Six Sigma, or Kaizen. cookies, Ritz, Wheat Thins and Triscuit crackers, and Swedish Fish and Sour Patch Kids confectionery products -are close at hand for our consumers across the country. Including many household names such as Oreo, belVita and LU biscuits; Cadbury Dairy Milk, Milka and Toblerone chocolate; Sour Patch Kids candy and Trident gum. We are proud to hold the number 1 position globally in biscuits, chocolate and candy as well as the No. 2 position in gum
We hold the distinguished position of being the largest 503A compounding pharmacy and FDregistered 503B outsourcing facility in the country serving the functional medicine markets. This position drives strategic quality initiatives and fosters cross-functional collaboration to elevate quality systems and current Good Manufacturing Practices (cGMP) compliance. Manages projects across functional teams including Regulatory Affairs and internal Businesses to standardize and enhance quality systems, audit readiness, and risk mitigation processes. Drives enterprise-level compliance with Food and Drug Administration, Drug Enforcement Administration, and other applicable regulations, ensuring a proactive quality culture across all departments and facilities. Project Management Professional (PMP) strongly preferred; Certified Quality Auditor (CQA); Certified Manager of Quality/Organizational Excellence (CMQ/OE) preferred.
Implements, maintains, verifies and validates the company’s SQF System; includes HACCP, Food Safety, Food Security and Food Quality. Aids in the development of Quality Control worker instructions, calibration procedures, test procedures, Statistical Process Control (SPC) interpretation, and computer set up and data input. Functions as a Safe Quality Foods (SQF) Practitioner; responsible for implementing, maintaining, verifying and validating of the Company’s SQF System; includes HACCP, Food Safety, Food Security and Food Quality. Required to possess or obtain certification as an SQF Practitioner. In addition to working at the world’s largest, state-of-the-art almond manufacturer, we offer a safe and collaborative team environment, with numerous opportunities for free training and career advancement.
As an employee owner, you directly receive the benefits of a job well done by being part of the Employee Stock Ownership Plan (ESOP).. Other benefits include Medical, Dental, Vision, HSA, FSA, Life Insurance, AD&D, Short Term Disability, 401(K), and an Employee Assistance Program.. Hours Worked: Normal hours are 8:00 AM to 5:00 PM, Monday-Friday with semi-regular travel or overnight stays expected.. Ability to acquire understanding of all applicable Department of Human Services and/or Department of Health rules and regulations and company policies.. Associate's degree in a field related to human services, and two years (4,160 hours) of full-time work experience providing direct care services to individuals with disabilities or individuals age 65 and older.
Stepan is currently seeking a Quality Manager to join our Leadership team in our Manufacturing facility in Anaheim, CA, reporting to the Regional Quality Manager. In addition, up to 6 lab technicians directly report to the Quality Manager. Strategy development and customer focus On-call support (off-hours and weekend) and up to 15% travelling as needed.. SQC, SPC, Six Sigma, and Continuous Improvement.. Established in 1932, Stepan Company is a major manufacturer of basic and intermediate chemicals including surfactants, polymers, as well as specialty ingredients that go into consumer, household, and institutional products such as laundry detergents, shampoos, and surface cleaners.
Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. Support all aspects of the Quality Management System (QMS) to ensure compliance with GMP, GLP, GCP, and other applicable GxP guidelines. Responsible for supporting Quality Operations in Batch record review, OOS, deviations, change controls and product complaint investigations and GxP archives. Support commercialization initiatives including implementation of Drug Supply Chain Security Act (DSCSA) serialization, develop commercial stage SOPs and Policies, and regulatory submissions.
- Adherence to corporate, State and Federal regulations and guidelines when handling hazardous materials or when exposed to hazardous situations. Support production improvements by utilizing SPC techniques and tools such as JMP. Language-Bilingual in English and Mandarin. B.S. in chemical engineering, materials science, physics or relevant education. Prior working experience in semiconductor industry is highly preferred.
Join our team at Morgan Rehabilitation and Healthcare Centeras an RN Supervisor / Quality Assurance Nurse!. Full-Time position - Monday through Friday with on-call weekend rotations. Primary series of the COVID-19 vaccine required.. A current, unencumbered active license to practice as an RN in the state of Rhode Island.. Employee assistance program (EAP) resources