11 hospital assistant jobs found

HIRING NOW: QUALITY ASSURANCE ASSISTANT INTERVIEWS AVAILABLE THIS WEEK** Interested in this role? Reach out directly to Grace Williams at grawilliams@actalentservices .com or CALL 317 567 6610 with an updated resume to apply Job Summary Join our team at one of the world's largest contract manufacturing facilities for active pharmaceutical ingredients (APIs) at our Lafayette facility. The work done here has made them one of the world's leading providers of drug delivery technologies. Job Essentials Help keep the QA document library organized and manage the technical documents from the facility so they can be properly accessed when needed. Review technical documents (Batch Records, SOPs, Training, Lab Protocols, etc.) and update document information as needed to ensure accurate documentation is QA library database. Prepare documents for off-site / on-site storage and send to appropriate locations when necessary under the guidance of the companies Document...

HIRING NOW: Quality Assurance Assistant Specialist INTERVIEWS AVAILABLE THIS WEEK** Interested in this role? Reach out directly to grawilliams @actalentservices .com or CALL 317 567 6610 with an updated resume to apply (HIRING NOW) Job Summary Join our team at one of the world's largest contract manufacturing facilities for active pharmaceutical ingredients (APIs) at our Lafayette facility. The work done here has made them one of the world's leading providers of drug delivery technologies. The facility is one of the world’s largest contract manufacturing facilities for active pharmaceutical ingredients (APIs) and is also second-largest site in the United States. This new site manufactures key pharmaceutical excipients for RNA-based therapies for innovative medicines and pandemic preparedness. Job Essentials Help keep the QA document library organized and manage the technical documents from the facility so they can be properly accessed when needed. Review...

At Bon Secours Mercy Health, we are dedicated to continually improving health care quality, safety and cost effectiveness. Our hospitals, care sites and clinicians are recognized for clinical and operational excellence. The Quality Assurance Specialist (QAS) is responsible for monitoring, assessing, and documenting the adherence to standards for programs and services delivered to consumers. The QAS monitors inbound and outbound interactions against a standardized evaluation tool designed to assess a service expert's adherence to scripts, system usage and customer experience. Responsible to provide input to the scoring methodology and form based upon updates to operational policies, procedures and system usage. Essential Functions Develop, maintain and implement processes and procedures to ensure delivery of service excellence, as well as make recommendations for enhancements to training materials or operational elements, as needed. Monitor and score service...

HIRING ASAP! If interested in more information/direct feedback, please reach out to me directly at ghilson@actalentservices. com and attach your resume and contact information. ?Below are some details about the position: BENEFITS:YES PAY: $42-50 an hour depending on experience SCHEDULE/ENVIRONMENT: On site (Potential of 5 hours of OT weekly) Job Description: We are seeking an experienced and detail-oriented Laboratory Technician to join a Hardware Failure Analysis team. This role supports failure analysis investigations by preparing and analyzing samples, troubleshooting issues with attention to detail, and assisting engineers by working through technical aspects of hardware failures. This role supports a Failure Analysis laboratory by enabling engineers to focus on root cause analysis rather than lab management and sample preparation. Daily activities include cutting, grinding, polishing samples, and setting up test equipment. Key Responsibilities...

Job Description We are seeking a dedicated Quality Assurance Document Specialist to ensure the integrity and accuracy of our documentation processes. This role involves reviewing batch records, completing records in accordance with standard operating procedures (SOPs), and managing quality documentation. The specialist will also be responsible for communicating findings to leadership. Responsibilities Review batch records regularly and ensure they are completed according to standard operating procedures. Manage and maintain quality documentation. Communicate findings and issues to leadership effectively. Qualifications Background in quality assurance. Proficiency in Microsoft Office applications. Detail-oriented with excellent handwriting skills. Ability to read and write in English. About Actalent Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives...

Responsibilities Create and update policies and procedures for quality control. Maintain ISO certification. Develop and update General Manufacturing Policies (GMP). Manage internal and external quality audits. Establish and update testing procedures, policies, and methods. Ensure testing equipment is properly calibrated. Maintain production records and documents. Record and retain material traceability. Update disposition of quarantined materials and determine material release. Handle change request forms and maintenance. Manage customer and internal specifications. Participate in the drawdown process with the Ink Department. Ensure staff completes necessary paperwork and data entry. Oversee and maintain accuracy of all records. Essential Skills Proven experience in quality assurance and quality control. Knowledge of ISO 9001 standards. Familiarity with manufacturing...

Quality Assurance Analyst/Specialist (231) Requisition ID 231 - Posted - PI-QA QA Prgrm - Carlsbad, NM, US - WIPP Site - Compliance ? Overview Be part of the nation's only repository for the disposal of nuclear waste known as Transuranic (TRU) waste. Salado Isolation Mining Contractors, LLC (SIMCO), managing and operating contractor of the Waste Isolation Pilot Plant (WIPP) is currently seeking qualified individuals to serve as Quality Assurance Analysts/Specialists and join our team located in Carlsbad, New Mexico. Responsibilities The successful candidate will be required to qualify as a NQA-1 Lead Auditor and perform assessments. Will be responsible for developing checklists, assessment plans, and assessment reports based on upper tier requirements. Perform quality assurance review of procedure and procurement documents for compliance with the applicable quality program requirements. Assist in the maintenance and development of the technical,...

Job Title: Quality Assurance SupervisorJob Description The Quality Assurance Supervisor is responsible for overseeing and enhancing quality control policies and procedures. This role ensures the maintenance of ISO certification and the creation and updating of General Manufacturing Policies (GMP). The supervisor will manage all quality audits and establish testing procedures, ensuring equipment is calibrated and production records are maintained. Responsibilities Create and update policies and procedures for quality control. Maintain ISO certification. Develop and update General Manufacturing Policies (GMP). Manage internal and external quality audits. Establish and update testing procedures, policies, and methods. Ensure testing equipment is properly calibrated. Maintain production records and documents. Record and retain material traceability. Update disposition of quarantined materials and determine material release....

Job Title: Quality Assurance Specialist Job Description As a Quality Assurance Specialist, you will perform quality checks on incoming raw materials, oversee in-process quality assessments, and conduct finished product evaluations. You will collaborate with production personnel to resolve issues and implement corrective actions, while meticulously documenting all quality-related information and maintaining an electronic Quality Management System (QMS). Additionally, you will assist with internal and external audits, manage the ISO program, and contribute to technical writing tasks based on quality checks and investigations. Responsibilities Conduct quality checks on incoming/raw materials, in-process, and finished products. Collaborate with production personnel to address issues and implement corrective action plans. Document all quality information and maintain electronic QMS. Perform document control and manage corrective actions, deviations, non-conformances, and...

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Summary Perform audits of basic records and reports and inspections of routine processes to assure compliance with applicable GLP regulatory requirements. Essential Duties And Responsibilities Assure Charles River’s compliance with applicable GLP . Communicate all identified compliance and quality risks to supervisor. Perform data audits to assess that records are attributable, legible, contemporaneous, original, accurate, and in compliance with regulations, SOPs, and protocols. Review SOPs,...

Job Title: Quality Assurance Associate Job Description We are seeking a dedicated Quality Assurance Associate to join our team. This role involves overseeing supplier quality management programs, auditing compliance, and developing quality agreements to ensure the highest standards in our manufacturing processes. Responsibilities Establish and maintain a Supplier Quality Management Program for CMOs, CTLs, 3PLs, raw material suppliers, and packaging component suppliers. Develop and maintain critical SOPs for supplier management, including supplier qualification, auditing, issue resolution, and change control. Monitor supplier performance through quality metrics, supplier evaluations, and risk assessments. Develop and maintain a supplier qualification and requalification process to ensure ongoing compliance. Plan, coordinate, and execute supplier audits to assess compliance with cGMP, ICH, and regulatory standards. Collaborate with...