Are you ready to make a meaningful impact in the world of cGMP Document Control operations? We're seeking a motivated individual to join our team at the Company’s Jump site as a Quality Assurance Document Control (QADC) Associate Specialist. Begin Your Career Adventure as a Quality Assurance Documen...
The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Jump site, including the document change control process, issuance and reconciliation of batch records, batch related forms, product labels, and management of archival and ...
The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the BMS Jump site, including the coordination, issuance, reconciliation, and management of production labels and records. Follow Policies, SOPs and work instructions to support the doc...
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A paid Product Tester position is perfect for those looking for an entry-level opportunity, flexible or seasonal work, temporary work or part-time work. ...
Provides administrative support for the department, including reception, secretarial, and clerical duties. ...
Conduct Quality on the Floor activities including quality walk-throughs of the production, testing and warehouse locations. GMP quality operations for the Bothell Manufacturing Plant (Jump). This role directly supports Jump’s release for infusion (RFI) timeline from the date of manufacture and will ...
The Facilities & Construction Administrative Assistant is responsible for providing God-Centric administrative and communication support to the Director of Construction and Vice President of Facilities & Construction. ...
As a Quality Assurance Specialist,. A minimum of 3 years of experience in pharmaceutical Quality Assurance, with direct experience in Quality Management Systems. Quality Management System performance metric preparation and reporting. Compile, contextualize, evaluate, and present Quality Systems data...
Join our Quality Systems team as a Quality Risk Management Specialist at our Bothell manufacturing facility. Job Title: Quality Risk Management Specialist. Understanding of Quality Risk Management principles and application within quality systems. This role is pivotal in maintaining our Quality risk...
Expert in training and advising junior administrative assistants on all matters pertaining administrative support provided to the Agency. BA/BS and 4 years' experience in administrative/business field OR AA and 6 years’ experience in administrative/business field OR HS Diploma and 10 years&rsq...
Quality Systems Specialist II . ...
Receptionist/Administrative Assistants to join our AWESOME Admin Team! Located in Bothell, our Admin and Client Services Team provides office and administrative support to the company to enable us to best meet the needs of our clients. Receptionist/Administrative Assistant Job Duties include:. ...
CGI Federal is seeking Quality Control (QC) Specialists who will be responsible for the daily monitoring of the Quality Management System (QMS) processes and performing QC checks in all functional areas. The QC Specialist is responsible for ensuring work on all projects is meeting all customer quali...
The Specialist will serve as a quality point of contact and quality subject matter expert for Real Estate and Facilities, Manufacturing, and Materials Management to ensure cGMP compliant operations at the site. The QA Specialist is responsible for Quality oversight of facilities, utilities, and ware...
Working from home near the office in Tumwater, Washington, the Administrative Assistant is responsible for daily school administrative tasks such as answering phones and email, communicating and updating records and student information systems, assisting the principals and teachers with administrati...
The assistant will report directly to the Director of Faith Formation. Additionally, the assistant must be able to make pastoral decisions as needed and provide professional communication to all who have dealings with the ministry and the parish. ...
Provide administrative support for pharmacy staff including preparation of correspondence, contacting patients, as well as screening incoming phone calls. Perform general administrative duties as needed. ...
This is your opportunity to start a lifelong career with unlimited opportunity.Discover the flexibility youve been searching for by taking a minute to finish our online application.No experience, Willing to train.Ability to work within recognized turnaround times.Must have exceptional social skills ...
Reporting to the Supplier Quality Assurance Director, you will be responsible for ensuring the quality of deliveries from our suppliers, in compliance with our standards and those of our customers. A smaller, dedicated team, they are focused on quality, consistency, and teamwork. With a strong focus...
A minimum of 3 years of experience in pharmaceutical Quality Assurance, with direct experience in Quality Management Systems (Veeva experience preferred). Quality Management System performance metric preparation and reporting. Compile, contextualize, evaluate, and present Quality Systems data and me...
Skills Provision is searching for a Document Control Coordinator for a company in the United States. The Documentation Control Coordinator is responsible for executing internal process. Control manufacturing documents, flow charts and work instructions. Assist in auditing information and answering q...
The primary focus of the Quality Control Specialist role to support product lot release and in-process testing within a cGMP environment. Require to work in and around laboratories and controlled, enclosed, restricted areas, included clean rooms. ...
About the Data Entry Research Participant position. This is an entry level position requiring no prior experiences. Review and verify for correctness all entered data. ...
Education: Associate degree or equivalent in Biology, Chemistry, or related field.Work Experience: 2+ years’ experience in a regulated manufacturing industry or equivalent combination of education and experience.Working knowledge of device/drug/biotech manufacturing processes.Detail oriented and abl...