Pay Range: $(27.00 – 30.00)/hr on W2 all-inclusive without benefits Shift Schedule: Monday – Friday (7 am – 4 pm or 8 am – 5 pm EST) Responsibilities: Oversight of QC in-process, release, raw material, and stability, and development samples, associated document management, and collection of data. Adherence to all GMP requirements, a proficiency in understanding of FDA/EMEA regulations, effective interactions/communication with Quality management, personal development, and support of investigations and inspections/audits. Manage sample tracking and the inventory system to track commercial and development samples. Generate sample submission forms for various testing facilities and process returned results. Collect sample forecasts to ensure lead time notice. Confirm testing was complete when sample invoices arrive. Follow/track international shipments, and alert logistics group of any customs clearance issues. Inspect incoming sample shipments and take necessary actions if samples do not comply with SOPs. Review and evaluate temperature data reports from temperature monitoring devices included with sample shipments. Execute protocols to support network stability, qualified material programs and pipeline product studies. Create and continuously improve sample management procedures and processes. Communicate with other departments and sites including Quality Assurance, Manufacturing and Facilities to address compliance issues and to implement corrective actions and to improve programs. Write and revise documents such as SOPs and technical reports. May support the Manager for activities related to training of employees, coordination of tasks, compliance with GMP, and identifying and implementing corrective and preventive actions. Support Stability sets and pulls including aliquoting and shipping during the study. Other related job duties as assigned. Requirements: High School degree with 6 years related experience in a GMP Quality Control Laboratory or Associate’s degree with 4 years related experience in a GMP Quality Control Laboratory or Preferred, Bachelors’ degree in a relevant scientific concentration plus 2 years related experience in a GMP Quality Control Laboratory. Possess a strong understanding of the requirements of sample receipt and inventory management in a GMP laboratory. Excellent oral and written communication skills with strong technical writing experience required. Able to work independently and effectively within the group, within Quality, and across the site. Ability to work in both paper based and electronic laboratory information management systems. #J-18808-Ljbffr
...Job Description Job Description SPECIAL EDUCATION ASSISTANT TEACHER The Shirley Aninias School | New York, NY | Full-Time, 12-Month | $45,000$55,000 ABOUT THE ROLE The Shirley Aninias School (SAS) is a private, 12-month, behavior-based elementary program...
...regulations and implementing federal market solutions that are timely, efficient, and legally effective. Centre has a vacancy for a Paralegal/Legal Assistant III. In this role, you will be supporting the overall mission of the United States Attorney's Office (USAO)....
...Role Description This full-time remote Software Engineer (Entry-Level) role involves designing, developing, and maintaining software solutions... ...environment. Qualifications Foundational knowledge in Computer Science, including algorithms, data structures, and software...
...Heavy Assembler Reports To: Manufacturing Supervisor FLSA Status: Non-Exempt (Hourly) Work Schedule: MondayThursday: 7:00 a.m. 3:00 p.m.; Friday: 7:00 a.m. 12:00 p.m. Overtime: Occasional approved overtime and weekend work may be required to meet...
...Selection is experiencing unprecedented growth, recently expanding in North Carolina. We are seeking an enthusiastic, experienced wine sales professional, looking to take their career to the next level, to join the team for on and off premises territories....