Quality Assurance Specialist Salary at Creativ-Ceutical BETA

Job Description Title: Quality Assurance Specialist Department: Payroll Reports To: Director, Payroll Salary Range: $52,280 - $70,373 Job Summary Participates in the development, implementation and maintenance of quality assurance plans. Conducts quality assurance reviews to ensure that work plans are executed in accordance with the School District of Philadelphia policies and procedures. Studies processes to determine cause and effect. Documents and evaluates data gathered and makes recommendations to the Director, Payroll. Essential Functions Identifies, recommends and implements changes to enhance the effectiveness of quality assurance strategies; assists with the development of quality assurance initiatives . Verifies allocation and calculation of leave days in accordance with District policies. Researches information on current and former School District of Philadelphia employees using the payroll system. Prepares and analyzes basic reports and provides the Director, Payroll with

At over 50 years old and counting, B&H has built a reputation as the trusted resource for photography and videography enthusiasts via its NYC SuperStore and its award-winning website. Long known as "The Professionals Source", B&H is recognized by savvy consumers worldwide for its honest, knowledgeable guidance, expert tips and articles and always-great prices. B&H offers competitive salaries, medical benefits, a 401K plan, employee discounts and opportunities to grow within a high-energy environment. Make your move to B&H today! Job Title: Receiving Quality Assurance Division/Department: Reports to: Approved By: Viewed By: Scheduled Hours: Monday-Thursday 9am-6pm, Friday 9am-3pm Last Reviewed: Job Overview: The Receiving QA Specialist is responsible for signing off on all incoming merchandise shipments in the warehouse. As a vital part of the receiving department, the warehouse receiving quality assurance specialist inspects the merchandise to ensure B&H has received what it was suppos

*Contract to hire* Shift is Tuesday – Friday 7:00 AM - 5:00 PM The Specialist II will support Quality Assurance lot release and disposition activities including process observation, batch record review, and completion of lot release documentation. The Specialist II supports QA initiatives including, but not limited to, review of laboratory investigations, deviation investigations, method validations, change controls, and CAPAs. The successful candidate will be able to effectively communicate bi-directionally in a complex, changing, and fast-paced environment. Essential Functions and Responsibilities Quality Assurance Operational Support: Perform QA Operation activities that include review of manufacturing batch records and labeling/packaging operations to ensure timely release of cell therapy products. Support quality assurance processes, controls and batch history files for QA Operations and Lot Disposition Perform real-time, on-the-floor support for manufacturing production activitie

Title: Quality Assurance Compliance Specialist Department: Quality Assurance Job Type: Regular Full Time Location: Horsham, PA/Hybrid – at least 3 days in the office Shift: Monday through Friday – 1st Company Summary: NMS Labs has developed an extensive menu of more than 2,500 Clinical and Forensic toxicology tests to support clients in healthcare, public health, and public safety fields. For over 50 years, our clients have relied on NMS Labs for unique testing solutions that demonstrate our company core values of Quality, Integrity, Service, Innovation and Engagement. As we work to increase the company’s positive impact on the diverse markets we serve, we are seeking talented professionals to join us for the journey! We invite you to learn more about our company by visiting NMSLabs.com. Job Summary: Under limited supervision, the Quality Assurance Compliance Technical Specialist will assist in monitoring regulated work conducted at NMS Labs for compliance with study protocols, interna

The Specialist I will support Quality Assurance lot release and disposition activities including process observation, batch record review, and completion of lot release documentation. The Specialist I supports Quality Assurance initiatives including, but not limited to, review of laboratory investigations and deviation investigations. The successful candidate will support internal teams and be able to effectively communicate bi-directionally in a complex, changing, and fast-paced environment. Shift: 2nd shift only - Tuesday-Friday (2:30PM - 12:30AM) Essential Functions and Responsibilities Quality Assurance Operational Support: Perform QA Operations activities that include review of manufacturing batch records and labeling/packaging operations to ensure timely release of cell therapy products. Support quality assurance processes, controls and batch history files for QA Operations and Lot Disposition Perform real-time, on-the-floor support for manufacturing production activities to ensu

The Specialist I will support Quality Assurance lot release and disposition activities including process observation, batch record review, and completion of lot release documentation. The Specialist I supports Quality Assurance initiatives including, but not limited to, review of laboratory investigations and deviation investigations. The successful candidate will support internal teams and be able to effectively communicate bi-directionally in a complex, changing, and fast-paced environment Essential Functions and Responsibilities Quality Assurance Operational Support: Perform QA Operations activities that include review of manufacturing batch records and labeling/packaging operations to ensure timely release of cell therapy products. Support quality assurance processes, controls and batch history files for QA Operations and Lot Disposition Perform real-time, on-the-floor support for manufacturing production activities to ensure compliance with GMP and GDP quality initiatives, escalat

CONTRACT-TO-HIRE MUST HAVES: BA/BS degree in life sciences discipline or equivalent 2+ years of biopharmaceutical industry experience or similar regulated environment Good Aseptic gowning background/experience Manufacturing/GMP experience Overview The Quality Assurance Specialist II will report to the Director, Quality Assurance Operations. The position will support the quality and regulatory compliance of commercial and clinical products including manufacturing, testing, and release at contract service providers. Further, the position will be responsible for ensuring that these operational activities are maintained in accordance with GMPs, global health authorities’ requirements and expectations. Shift: Wednesday to Saturday from 7:00 AM - 6:00 PM. (4 days - 10 Hours Shift) Essential Functions and Responsibilities Represent QA by working on-site at the CMO for up to 5 days per week. Support CMO manufacturing, testing, and release activities on weekends, as needed. Establish and mainta

Summary See below for important information regarding this job. Additional vacancies may be filled from this announcement. Responsibilities Perform duties associated with the administration of the quality assurance provisions of contracts by designing, implementing, and maintaining a risk-based surveillance program and assessment plan. Identify opportunities for process improvements through analysis of process measurement data. Serves as a member of a multi-functional or technical team. Responsible for implementing the overall Quality Program for a diversity of products and services in support of U.S. Government acquisition at one or more suppliers facilities. Ensure contractors comply with all requirements related to the design, manufacturing, repair, overhaul, and modernization of a variety of items for contractor and customer activities throughout the world. Independently audit and survey contractors processes to ensure customer and contractual requirements are met. Investigate and