2nd or 3rd Shift - Associate or Mid-Level Product Review Engineer (Liaison Engineering) Boeing2nd or 3rd Shift - Associate or Mid-Level Product Review Engineer (Liaison Engineering)North Charleston, SC$85,000–$140,300 / yearThe Boeing Company also provides eligible employees with an opportunity to enroll in a variety of benefit programs, generally including health insurance, flexible spending accounts, health savings accounts, retirement savings plans, life and disability insurance programs, and several programs that provide for both paid and unpaid time away from work. This position involves daily exposure to a factory environment which includes stairs, trip hazards, high noise areas, chemical hazards (breathing and handling), and entering airplanes during their many stages of building.
Registered Nurse Supervisor - 3rd shift (OIDD - Coastal) State of South CarolinaRegistered Nurse Supervisor - 3rd shift (OIDD - Coastal)Dorchester County, SC$85,000–$93,823 / yearEmployment Contingency: Employment is contingent upon our receipt of the following required pre-employment screenings: medical screening - to include a drug screening; background record checks (to include fingerprinting), South Carolina Department of Social Services' Child Abuse and Neglect Central Registry screening, U.S. Department of Health and Human Services Office of Inspector General "List of Excluded Individuals/Entities" screening; South Carolina Department of Motor Vehicles Driving Record check; and a review of transcripts verifying educational credentials. The South Carolina Department of Behavioral Health and Developmental Disabilities, Office of Intellectual and Developmental Disabilities offers an exceptional benefits package for FTE positions that includes: The South Carolina Department of Behavioral Health and Developmental Disabilities, Office of Intellectual and Developmental Disabilities offers an exceptional benefits package for FTE positions that includes: Health, dental, vision, long-term disability, and life insurance for employees, spouse, and children.
Packaging Machine Technician I, 3rd Shift Bausch & Lomb IncPackaging Machine Technician I, 3rd ShiftGreenville, SCWe have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life.
Inventory Cycle Counter 3rd Shift Fresh ExpressInventory Cycle Counter 3rd ShiftColumbia, SCFull time3rd Shift 10:00pm - 7:00am The Inventory Cycle Counter is responsible for maintaining accurate inventory data in PRMS and providing support as needed in the Inventory department. This requires daily cycle counting and inventory maintenance, packaging, film, condiment, trailers and Finished Goods inventories.
Process Engineer - Paint Robotics (3Rd Shift) Oshkosh Corp.Process Engineer - Paint Robotics (3Rd Shift)Spartanburg, SC$64,500–$103,500 / yearHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with Oshkosh Corporation's legal duty to furnish information. Research and formulate plans to accomplish major projects, including manpower estimates, cost estimates and work measuring devices such as milestones or critical path charts.
NewRECORDS SPECIALIST-3RD SHIFT-FT Greenville County South CarolinaRECORDS SPECIALIST-3RD SHIFT-FTGreenville, SCProcesses a variety of documentation associated with department/division operations; review and processing of law enforcement reports; performs data entry functions involving various computer applications to include entry and updates to law enforcement reports. Verifies accuracy of entered data and processed documents; conduct research for criminal justice agencies; performs customer service functions regarding department/division operations.
Production Operator 3rd shift Kyocera AVX Components CorpProduction Operator 3rd shiftFountain Inn, SCAs a wholly owned subsidiary of KYOCERA Corporation structured to capitalize on shared resources and technical expertise, KYOCERA AVX has an expansive global footprint comprised of several dozen research, development, and manufacturing facilities spanning more than 15 countries and staffed with talented personnel dedicated to innovation, component quality, customer service, and enabling a brighter future through technology. KYOCERA AVX designs, develops, manufactures, and supplies advanced capacitors, antennas, connectors, circuit protection and timing devices, sensors, controls, filters, fuses, diodes, resistors, couplers, and inductors optimized for employment in the international 5G, IoT, aerospace, automotive, consumer electronics, industrial, medical, and military markets.
UNIV - Clinical Research Sponsor Invoicing Analyst - Office of Clinical Research, OVPR Medical University of South CarolinaUNIV - Clinical Research Sponsor Invoicing Analyst - Office of Clinical Research, OVPRSouth CarolinaIn collaboration with department/division Grants Administrators, Principal Investigators and study teams, Research Administration and Grants and Contracts Accounting Offices, this position will coordinate industry sponsored study invoicing, billing and reconciliation activities to ensure that all earned revenue is realized under this OCR fee for service program and provide training, mentorship and guidance for sponsor invoicing within MUSC’s Clinical Trial Management System. Experience as a clinical research coordinator, research nurse coordinator, research/sponsored programs accountant, grants administrator, or professional accountant/financial analyst with direct industry sponsored research experience preferred, or an equivalent combination of experience, education and training.
UNIV - Clinical Research Sponsor Invoicing Analyst - Office of Clinical Research, OVPR MUSCUNIV - Clinical Research Sponsor Invoicing Analyst - Office of Clinical Research, OVPRSouth CarolinaIn collaboration with department/division Grants Administrators, Principal Investigators and study teams, Research Administration and Grants and Contracts Accounting Offices, this position will coordinate industry sponsored study invoicing, billing and reconciliation activities to ensure that all earned revenue is realized under this OCR fee for service program and provide training, mentorship and guidance for sponsor invoicing within MUSC’s Clinical Trial Management System. Experience as a clinical research coordinator, research nurse coordinator, research/sponsored programs accountant, grants administrator, or professional accountant/financial analyst with direct industry sponsored research experience preferred, or an equivalent combination of experience, education and training.
Registered Nurse (RN) Research, Clinical Research, FT, Days Prisma HealthRegistered Nurse (RN) Research, Clinical Research, FT, DaysGreenville, South CarolinaProvides patients/families with information regarding clinical trial participation and provides education regarding individual treatment including purpose, potential side effects, and self-care measures, documents interaction. Collaborates with the IRB of record and sponsoring agencies as well as local agencies, when applicable, to ensure global awareness regarding the progression of various studies, amendments and regulatory monitoring.
Clinical Research Assistant Opportunities - Multiple Locations Nationwide Headlands ResearchClinical Research Assistant Opportunities - Multiple Locations NationwideMyrtle Beach, SCThis general interest posting is designed for Clinical Research Assistants (RAs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. We welcome interest from candidates who bring: A bachelor's or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or.
UNIV - Clinical Research Assistant - Surgery: Clinical Trials MUSCUNIV - Clinical Research Assistant - Surgery: Clinical TrialsCharleston, South Carolina$37,200–$48,300 / yearNote: The following descriptions are applicable to this section: Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift; Infrequent - 0-2 hours per shift) Ability to perform job functions in an upright position. This person will also conduct all research in adherence with the FDA Code of Federal Regulations, "Good Clinical Practices”, and adhere to the MUSC IRB regulations for the protection of human subjects.
UNIV - Clinical Research Assistant - Surgery: Clinical Trials Medical University of South CarolinaUNIV - Clinical Research Assistant - Surgery: Clinical TrialsCharleston, South CarolinaNote: The following descriptions are applicable to this section: Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift; Infrequent - 0-2 hours per shift) Ability to perform job functions in an upright position. This person will also conduct all research in adherence with the FDA Code of Federal Regulations, "Good Clinical Practices”, and adhere to the MUSC IRB regulations for the protection of human subjects.
UNIV - Research Program Assistant - Advance - Department of Dermatology Medical University of South CarolinaUNIV - Research Program Assistant - Advance - Department of DermatologyCharleston, South CarolinaThis position assists investigators and research staff with participant recruitment, scheduling, data management, regulatory documentation, and study coordination activities while ensuring compliance with institutional, sponsor, IRB, and federal requirements. Physical Requirements: (Note: The following descriptions are applicable to this section: Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift; Infrequent - 0-2 hours per shift) Ability to perform job functions in an upright position.
Iach Research Assistant Furman UniversityIach Research AssistantGreenville, SCThe position will assist with research activities such as scheduling meetings and taking meeting minutes, IRB submission and amendments, literature reviews, data collection, data cleaning, descriptive data analysis, and reporting. Relationships: Continuous contact with members of own work unit to plan, coordinate, problem solve, exchange information, and make suggestions related to mutual and institutional goals.
IACH Research Assistant Furman UniversityIACH Research AssistantSCThe position will assist with research activities such as scheduling meetings and taking meeting minutes, IRB submission and amendments, literature reviews, data collection, data cleaning, descriptive data analysis, and reporting. Relationships: Continuous contact with members of own work unit to plan, coordinate, problem solve, exchange information, and make suggestions related to mutual and institutional goals.
Research Assistant CLEMU Clemson UniversityResearch AssistantSeneca, South CarolinaAdditional responsibilities may include: recruiting and screening older adult participants; administering informed consents, behavioral assessments, and study interventions; collecting, entering and analyzing data; ensuring compliance with all regulatory and reporting requirements; and possible outreach activities. The position is a staff role in Clemson University's Institute for Engaged Aging, with a dynamic team dedicated to the Institute's mission to find and share the best ways to support and enrich the lives of older adults through research, education and community outreach.
Clinical Research Associate Ii/Iii Novotech Health Holdings Pte LimitedClinical Research Associate Ii/IiiCharleston - Office, SC$70,000–$140,000 / yearPreferably experience of working in the research, pharmaceutical industry or a related field per job level as follows: CRA II: Approximately 1-2 years of Clinical Research Associate experience or equivalent experience (CRA II fast track) in other roles in the Clinical industry. Provide written and verbal site updates (including monitoring visit reports) on study progress to the PM/LCRA according to the study requirements/timelines as documented in the Clinical Monitoring Plan and Sponsor/Novotech SOPs.
Program Mgr-Non-Sponsored Clinical Research Spartanburg Regional Healthcare SystemProgram Mgr-Non-Sponsored Clinical ResearchSpartanburg, SCThe Manager of Clinical Research Program (Non-Sponsored) works closely with the Director of Clinical Research, Graduate Medical Education (GME) leadership, residency program directors, faculty mentors, Research Compliance, and health system leadership to develop and sustain a scalable model for resident/fellow research and quality improvement support. The manager oversees day-to-day operation of the resident research and QI support program, including workflow coordination, process development, and strategic planning to ensure consistent and high-quality support for resident-fellow scholarly activity and quality improvement work.
Program Mgr-Non-Sponsored Clinical Research Spartanburg Regional Medical CenterProgram Mgr-Non-Sponsored Clinical ResearchSpartanburg, SCThe Manager of Clinical Research Program (Non-Sponsored) works closely with the Director of Clinical Research, Graduate Medical Education (GME) leadership, residency program directors, faculty mentors, Research Compliance, and health system leadership to develop and sustain a scalable model for resident/fellow research and quality improvement support. The manager oversees day-to-day operation of the resident research and QI support program, including workflow coordination, process development, and strategic planning to ensure consistent and high-quality support for resident-fellow scholarly activity and quality improvement work.