Average salary: $101,906 /yearly
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- Shift Schedule is 2100-0730, Wednesday-Saturday The Quality Associate II position plays a key role in supporting the cGMP quality operations... ...within a regulated cGMP environment. The primary focus of the QA Associate role will be to support routine clinical and...SuggestedShift work
- Work Schedule: Wednesday - Saturday, 6AM - 4:30PM PST Maintains shop floor quality presence; disposition in-process materials and finished product; investigates and resolves GDP errors; performs batch record reviews. Assures the quality of manufactured products are in ...Suggested
- An established industry player is seeking a dedicated Quality Assurance professional to ensure compliance with manufacturing regulations. This role involves reviewing batch production records, monitoring processing stages, and supporting audits to maintain product quality...Suggested
- Job Title: QA Associate Specialist Document Control Location: Bothell, WA - ONSITE Part of the JUMP Project Initiative Top Skills: EDMS Experience. Preferably 3-5 years. Systems include VIVA, Master Control, & Documentum etc. Ability to manage competing priorities Teamwork...SuggestedShift work
- ...AND SCOPE OF POSITION (Position Summary): The Quality Assurance (QA) Specialist position plays a key role in supporting the cGMP... ...facilitating/leading triages, reviewing necessary data and information associated with the deviations with no impact and determining the...SuggestedFor contractorsImmediate start
- An established industry player is seeking a detail-oriented Specialist to support the QA Disposition group. This role involves ensuring compliance with corporate policies and cGMP standards while managing quality records and documentation. The ideal candidate will possess...Suggested
- Job Title Major duties and responsibilities: Quality Management System performance metric preparation and reporting. Compile, contextualize, evaluate, and present Quality Systems data and metrics. Investigation & CAPA Review Board Administrator. Compile slides...Suggested
- An established industry player is seeking a Quality Assurance Document Control Associate Specialist to enhance their cGMP Document Control operations. In this pivotal role, you will manage document change control processes, oversee batch records, and ensure compliance with...Suggested
- Quality Assurance Document Control (QADC) Associate Specialist Job #: 3240 Pay Rate: Not Specified Job type: Location: Bothell, WA Top Skills: Strong communication and customer service skills. Innovation Able to prioritize, manage time well, multi-task, and troubleshoot...SuggestedLocal areaShift work
- An established industry player is seeking a Quality Assurance Specialist to enhance cGMP quality operations at their Bothell facility. This role is pivotal in managing deviations, conducting investigations, and ensuring compliance with regulatory standards. The ideal candidate...Suggested
- Job Duties: ~5+ years in Quality Assurance/Testing with specialization in Telecom Domain covering areas e.g. Device Financing, Accounting, Service Accounting, Risk Management (Credit, Fraud, Controls), Tax, Business Assurance etc. ~ Experience in Amdocs, and or ...SuggestedWork experience placement
The Dignify Solutions LLC
Seattle, WA2 days ago - A biopharmaceutical company in Washington is seeking a QA Specialist to oversee quality assurance operations in GMP manufacturing. This role involves reviewing quality events, developing training programs, and ensuring compliance with regulatory standards. The ideal candidate...Suggested
- A leading biopharmaceutical company in Redmond is seeking a QA Specialist for QMS Operations. The role involves executing QA responsibilities in GMP manufacturing, collaborating across teams, and enhancing quality systems. Ideal candidates will have a bachelor's degree...SuggestedFlexible hours
- A biopharmaceutical company in Redmond seeks a passionate QA Specialist to manage quality assurance responsibilities within GMP manufacturing. You will collaborate across teams, ensuring compliance with regulatory requirements and internal procedures. Ideal candidates...SuggestedFlexible hours
$83k - $86.25k
Job Title: QA Specialist - QMS Operations Location: Redmond, WA, limited travel to Seattle site. Shifts: Days, Monday to Friday. 8am till 5pm core hours. About Us: this is who we are At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation...SuggestedHourly payTemporary workMonday to FridayFlexible hoursShift work$20.77 - $26 per hour
A leading company in quality assurance is seeking a Quality Assurance Administrator to support compliance and enhance quality processes. This role requires a high school diploma (or GED) and offers on-the-job training with no previous experience necessary. Responsibilities...Hourly payFull time- A biopharmaceutical company in Redmond is seeking a Senior QA Specialist in Document Control to ensure compliance with cGMP expectations and company SOPs. The successful candidate will be responsible for issuing production records, managing document control, and supporting...Flexible hours
- A technology company is looking for a Proofreader to join its team in Seattle. The successful candidate will have 1-3 years of experience in proofreading within a high-volume, deadline-focused environment. You'll be responsible for ensuring text quality by checking documents...Full time
- A leading marketing solutions provider in Seattle is seeking a Marketing Campaign Operations Specialist to execute performance marketing campaigns. This temporary role involves manual tasks such as campaign setup, testing, and reporting. Ideal candidates have over 3 years...Temporary work
- A leading biopharmaceutical company in Redmond is seeking a passionate QA Specialist to join their team. This role involves executing QA responsibilities for GMP manufacturing and enhancing quality assurance systems. Ideal candidates will have a Bachelor's degree, at least...Flexible hours
- A leading biopharmaceutical company in the United States is seeking a QA Specialist for QMS Operations. This role involves day-to-day QA responsibilities in GMP manufacturing and enhancing quality assurance systems. Candidates should possess a Bachelor’s degree in biological...Flexible hours
- A technology consulting firm is seeking an experienced iSeries QA to ensure the quality of software in an Agile environment. The candidate must possess at least 3 years of QA experience, with a strong focus on iSeries testing and familiarity with HP ALM tools. Responsibilities...
- JOB TITLE: QC Associate Location: Bothell, WA - 100% onsite TOP Skills: Bachelor's degree in life or physical sciences Strong analytical and communication skills. Computer proficiency as well as the ability to master new software programs. The ability to work effectively...
- Job Title: Training Specialist Must Have List: Bachelor's degree, 3 years of professional experience in developing and delivering technical training, 2 years of professional experience working in a CGMP or regulated environment, 3 years of experience with MS Office,...
Omni Inclusive
Bothell, WA4 days ago $65k - $95k
...standards of quality, safety, and client satisfaction. To maintain our commitment to excellence, we are seeking a Remote Quality Assurance (QA) Specialist/Engineer to oversee our project workflows, ensure regulatory compliance, and enhance quality processes from a remote...Remote jobFull timeLocal areaFlexible hours- An established industry player is seeking a detail-oriented QA Associate Specialist to enhance their Document Control operations. This role is vital in supporting the cGMP Document Control processes, including document approvals and change control. The ideal candidate...
- A leading global workforce solutions company is seeking a Data Collection Technician specializing in Dutch language. This role involves guiding participants through studies, conducting quality assurance audits, and authoring data collection guidelines. The successful candidate...Contract work
- An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP Document Control operations. This role involves managing an electronic document system, ensuring compliance with regulatory standards, and supporting audits...
- A leading educational institution is seeking a Program Operations Specialist to join the Clinical Trials Office. This position involves managing billing compliance for clinical trials, analyzing systems processes, and providing exceptional customer service. The ideal candidate...Work at office
$48.4k - $72.6k
...Specialist II is responsible for overseeing Premera's compliance with corporate audit programs such as the Blue Cross Blue Shield Association (BCBSA) Member Touchpoint Measures (MTM) and Licensee Desk Level Audit (LDLA), the Federal Employee Program (FEP) audit and tier...Work experience placementPremera Blue Cross
Mountlake Terrace, WA3 days ago
