Pharma/Scientific - Quality Control Associate - Bothell

We are seeking a Document Control Associate to support our cGMP Document Control operations for client Jump site records management. · The successful candidate will be responsible for receiving and reconciliation of GMP records, management of scanning, archival and retention of G ...

The manager is looking for level II or level III Quality Control Associate. · *Experience with PCR and Microplasma is a must · The primary focus of the Quality Control Associate II/III role will be to support product lot release and in-process testing within a cGMP environment.,B ...

The primary focus of the QC Associate I role will be to provide lab support functions within Juno's Quality Control Microbiology group including: · ...

The Quality Control Associate I role provides lab support functions within Juno's Quality Control Microbiology group. · Monitor all clean room environments throughout the facility. · Perform tests relevant to microbiology lab as required. · ...

The primary focus of the QC Associate I role will be to provide lab support functions within Juno's Quality Control Microbiology group including: Monitor all clean room environments throughout the facility, · Responsible for performing all the tests relevant to microbiology lab a ...

The Quality Assurance Document Control (QADC) Records Coordinator will perform compilation and archival of GMP documents/records related to Manufacturing Operations ensuring original records security, facilitate data integrity, ensure easy/timely retrieval of records, and support ...

+This is an entry-level Quality Control Laboratory Technician role at Juno headquarters in Seattle. The candidate will perform preventative maintenance & equipment onboarding for QC labs. · ...

The Quality Assurance - Records Management supports the cGMP Document Control operations for Client Bothell site records management. · ...

We are hiring for an Urgent HOT Job in Bothell, WA. · The primary focus of the Quality Control Associate I role will be to support raw material testing and release within a cGMP environment. · ...

The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Jump site. · Issuing production batch records. · Responsible for the organization of cGXP controlled document files within the Document Center and ensur ...

The primary focus of the Quality Control Associate I role will be to support drug product lot release and in-process testing within a cGMP environment.Perform or support cGMP lot release, · in-process,and stability testing using various software packages. · ...

We are seeking a highly motivated Research Associate to support Quality Control (QC) testing of potency assays for our Antibody Drug Conjugate (ADC) portfolio. · The primary responsibility of this role will be the execution of routine QC potency testing in support of release and ...

We are seeking a highly motivated Research Associate to support Quality Control (QC) testing of potency assays for our Antibody Drug Conjugate (ADC) portfolio. · Perform routine QC potency testing for ADC products. · In collaboration with Contract Testing Labs (CTLs), develop rob ...

We are seeking a highly motivated Research Associate to support Quality Control (QC) testing of potency assays for our Antibody Drug Conjugate (ADC) portfolio. · Opportunity to contribute directly to clinical-stage programs while gaining exposure to assay development qualificatio ...

+We are seeking a highly motivated Research Associate to support Quality Control (QC) testing of potency assays for our Antibody Drug Conjugate (ADC) portfolio.+ · +Perform routine QC potency testing for ADC products... · ...

We are seeking a highly motivated Research Associate to support Quality Control · (QC) testing of potency assays for our Antibody Drug Conjugate (ADC) portfolio.The ideal candidate will have hands-on experience with ADC cell-based potency assays, · strong attention to detail and ...

Serves as a point-of-contact for inventory-related tasks and issues in a distribution center Operates material handling equipment to move inventory within the facility. · ...

The position involves compilation and archival of GMP documents/records related to Viral Vector Manufacturing. · Reviews existing file set up for paper GMP records related to Plasmid and Vector lot disposition. · Organizes and associates related paper documents/records into a sin ...

Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases.The Associate Director, Quality Control will lead critical Quality Control functions to support Jade's product pipelin ...

This job is responsible for overseeing critical reagent and raw materials in support of global method transfer activities across global product quality. · Managing key deliverables associated with clinical and commercial critical reagent / raw material needs across multiple progr ...