Qc Salary at Healthcell BETA

Job Title: Quality Specialist I Job Description The individual will work primarily in the Quality Control Laboratory to support the testing and analysis of cGMP produced viral vectors and cells. The Quality Specialist I will collaborate closely with the QC manager and senior QC staff to cultivate and enact strategic direction in the GMP area. Responsibilities include running sample assays five nights a week, performing the proper operation, calibration, validation, cleaning, and maintenance of QC lab equipment, and assisting with the manufacturing of viral vector products. Responsibilities Perform QC methods and develop new methods under senior staff guidance. Analyze microbiological environmental monitoring samples. Write and revise Standard Operating Procedures (SOPs). Maintain and monitor QC lab equipment. Manage QC and Production supplies. Conduct periodic cleaning of clean room facility. Assist in the manufacturing of viral vector products periodically. Operate within the Quality

Healthcare Project Architect Join GPD Group, where our purpose is to improve the well-being of our employees, clients, communities, and business partners by transforming opportunities into success. We are passionate about the work we do and the relationships we build with clients. Our employee ownership structure fosters a non-hierarchical collaborative work environment, where everyone is encouraged to share their ideas and creativity to the betterment of the organization and our clients. This structure also enables each associate to explore and expand their talents, reach their full potential, and deliver to the core traits that guide GPD group and allow us to deliver successfully for our clients. For more than 60 years, GPD Group has been providing architectural, engineering and planning services to clients across the United States. With a diverse team of over 700 professionals working in 13 different offices, it is our passion for our work and our commitment to our purpose that unit

MMR Constructors, Inc. A subsidiary of MMR Group, Inc. Job Location: Lancaster, Ohio Job Duration: 8 months Job Schedule: 58 hours a week (M-F 10-hour shifts and one 8-hour shift on Saturday) Salary/Hourly, Per Diem: Hourly Rate $36 an hour $700 a week per diem MMR Group is seeking a project QC Inspector with both industrial and heavy commercial construction experience. The responsibilities would include, but not limited to, the following: •Administration of the Quality Management System (QMS) outlined in the MMR PQP •Organizational freedom to recognize quality problems and to provide solutions to these problems •Perform the various periodic project jobsite audits as required •Review provided drawings, specifications, approved RFI's and submittals, etc. for quality requirements •Conduct and record all MMR quality inspection and testing activities on the appropriate Inspection and Test Reports as required •Coordinate ITP audit, hold, monitor, and witness points with client, owner, engin

Required Skills: Project Management - Managing the Overall Project with strong knowledge in GIS. Competent in analyzing GIS data, preparation of gap reports, and designing QA/ QC procedures for data validation Preparing data models, platform migration plans, planning, assigning, and monitoring tasks to team members. Understanding of various GIS data models and mapping the client requirements with the various business functionalities Strong Communication Skills is mandatory

Job Description: Hands on experience on writing exceptional and complex SQL queries and procedures. Hands on experience on using tools like JIRA, HP QC ALM etc.. Experience to work with the teams on global presence. Excellent communication skills (verbal and written) . Should be able to work independently to result high quality deliverables, covering both functional and non functional requirements. Perform unit testing and peer review of the code. Write and deliver release installation instructions, technical specifications document, low level design documents. Work with internal teams and client resources to be able to assist in release migrations. Job Responsibilities: Understand the cardinality of the data and produce specific events required To visualize the preprocessing required on GCP and support deriving I/O mapping required along with BA Work with GCP and Big Data, design and implement data pipelines, and ensure data quality and integrity Emphasize the logical structures of th

Position Overview: Ensures the quality of the site installations is consistent with the company’s policy requirements together with national and international standards and the customers specifications. Essential Job Functions: Implement the QA/QC management system at site with the project team. Coordinate with project team quality inspections with all the site subcontractors and vendors. Assist the project team coordination of nondestructive testing. Coordinate with project team and the customers representative on all quality matters. Assist project team distribution and resolution of QA/QC task reports for site subcontractors. Verify that quality related site activities are in accordance with contract documents and the applicable standards. Participate, conduct and manage site audits to ensure project team is meeting expectations of corporate QAQC policy. Coordinate with project team all the quality site inspections conducted by AE, Owner representative, etc. and integrate into Elfor

Affiliated Engineers, Inc. (AEI) is a leading, multidisciplinary consulting engineering firm and collaborative community of over 800 employees who plan, design, and deliver high-performance, innovative, and holistic engineering solutions - positively impacting society and advancing humankind. Recognized in the Top 20 Engineering Firms and Top 3 Science and Technology Firms since 2000 by Building Design + Construction Magazine, AEI is dedicated to enhancing public health and improving patient outcomes, advancing revolutionary biomedical research, and enabling the next generation of scientific discovery and technological innovation through remarkable design and award-winning projects. From collaborating with the California Air Resources Board to transform air quality in the world's largest, zero net energy emissions testing facility to creating human-centric, technically advanced clinical environments that elevate communities - such as Healthcare Design Magazine's 2022 Design Showcase Wi

Quality Specialist Job Description The individual will work primarily in the Quality Control Laboratory to support the testing and analysis of cGMP produced viral vectors and cells. The Quality Specialist I will collaborate closely with the QC manager and QC staff to cultivate and enact strategic direction in the GMP area. Responsibilities include running sample assays five nights a week, performing the proper operation, calibration, validation, cleaning, and maintenance of QC lab equipment, and assisting with the manufacturing of viral vector products. Responsibilities Perform QC methods and develop new methods under senior staff guidance. Analyze microbiological environmental monitoring samples. Write and revise Standard Operating Procedures (SOPs). Maintain and monitor QC lab equipment. Manage QC and Production supplies. Conduct periodic cleaning of clean room facility. Assist in the manufacturing of viral vector products periodically. Operate within the Quality Management System ap