Job Summary The Inventory Control and Quality Assurance (ICQA) Associate will play a critical role in ensuring inventory accuracy and product quality for NAPA’s automotive parts aftermarket in the distribution center. Reporting to the ICQA Manager,
Core Hours Monday - Friday, 8:00 am - 5:00 pm Purpose and Scope The Senior Quality Validation Engineer is responsible for driving validation initiatives and execution across multiple systems and processes in a sterile injectable manufacturing
Kodak Alaris is a global technology company that’s delivering future value through customer solutions. Our advanced, patented intellectual property combines breakthrough technologies, digital transformation, and human know-how to unlock the power of images and information. We
Work ScheduleFirst Shift (Days) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work
Overview Company Overview WuXi STA is building new pharmaceutical manufacturing capability and is establishing the quality systems that will support it. For more information, see: New manufacturing facility announcement About the company Responsibilities The Quality Assurance
Capital Health is the regions leader in providing progressive, quality patient care with significant investments in our exceptional physicians, nurses and staff, as well as advanced technology. Capital Health is a dynamic health care resource accredited
SUMMARY: Under supervision of the Manager Laboratory Outreach Services or guidance of the Lead Phlebotomist, performs responsibilities associated with obtaining blood and various other patient specimens in accordance with department procedures. Obtains samples ordered by physicians
General • Responsible and accountable at all times for operating in the best interest of the Company. • Maintains a positive representation of Company at all times, including the name, integrity, culture and concept of the
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources
Overview Operator I supports cGMP pharmaceutical manufacturing activities by executing batch operations, cleaning and setup, in-process checks, and documentation with a strong focus on safety, quality, and right-first-time performance. This role is fully trained to operate
Core Hours Monday - Friday, 8:00 am - 5:00 pm Purpose and Scope The Validation Engineer II is responsible for independently planning, executing, and documenting validation activities in a sterile injectable manufacturing environment. Responsibilities include equipment,
Overview We are seeking a highly experienced Principal Engineer - Equipment Integration and Technical Services to serve as the site technical authority for process equipment design, equipment-to-facility integration, and lifecycle technical support at the Middletown drug
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold
WHERE YOU WILL WORK Without compromising our steadfast commitment to Quality, Safety and Sustainability our manufacturing and packaging facility produces in excess of 70MM units per year. This is a demonstration of our can-do attitude, collaborative
Work ScheduleSecond Shift (Afternoons) Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Position: Industrial Multi-Craft Maintenance Technician Location: Middletown, VA Shift: 2nd Shift (2:30 pm
Associate Director, Trial Master File (TMF) Position Summary The Associate Director, Trial Master File (TMF) will report to a senior leader within Clinical Development Operations and is responsible for the strategic oversight, governance, and continuous improvement
Retirement Benefits Specialist II Bring your communication, problem-solving, and office management skills to Sonoma County Employees Retirement Association (SCERA)! Starting salary up to $41.60/hour ($86,824/year) and a competitive total compensation package! Join Our Team The Sonoma
Advanced Optical Development Lead VIAVI Solutions has a 100+ year history of technical innovations that have evolved to keep pace and address our customers most pressing business issues. We make equipment, software, and systems that help
Senior Project Manager, MEP Projects As a Senior Project Manager Lead at Turner & Townsend, you will play a pivotal role in delivering complex, critical environment projects for a key tech client. You will be responsible
ER RN Fusion Medical Staffing is seeking a skilled ER RN for a 13-week travel assignment in Santa Rosa, California. As a member of our team, youll have the opportunity to make a positive impact on