QA Associate
$31 - $34.22 per hourBristol-Myers Squibb
Responsibilities 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 compliance with all applicable regulations and guidelines. May assist in preparing for hosting of regulatory and customer audits. Performs general and/or more complex manufacturing formulation batch production record reviews and approvals in support of product release in accordance with specifications and SOPs. Inspects and releases intermediates or packaged drug product per specifications. Monitors various stages of processing along with the appropriate paperwork in compliance with specifications. Monitors and trends batch record errors and provides Quality Assurance management with quality indicator data. Provides site-wide support during daily walkthroughs of GMP areas. Qualifications Documentation Review experience Scientific Degree Experience working in a GMP environment Okay with candidates out of college who have a biology or similar degree who are looking for GMP experience Requirements B.S., in Biology, Chemistry or related discipline, or its equivalent is preferred 2 years of relevant experience in a regulated environment with at least 2 years focused on quality assurance function Knowledge of pharmaceutical or biotech product manufacturing Knowledge of US and EU cGMP regulations and guidance Knowledge of SAP or equivalent ERP System; BMRAM, MES, Veeva or TrackWise systems are a plus Role may entail use of disinfection agents (such as IPA or Sporklenz), gowning/PPE requirements to enter clean room spaces and handling of blood-based drug products Details 100% onsite Work Schedule: Wednesday – Saturday, 6:00 AM – 4:30 PM PST (Shift: 4 x 10 h) Contract assignment with ASK Staffing to provide services to Bristol Myers Squibb Compensation: starting range $31.00 – $34.22 per hour. Final compensation determined by employer of record based on assignment characteristics, experience, skills, and location #J-18808-Ljbffr
- ...Quality - QA Associate Specialist Document Control Job #: 4934 Pay Rate: Not Specified Job type: contractor Location: Bothell, WA PURPOSE AND SCOPE OF POSITION: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations...SuggestedFor contractors
TechDigital Group
Bothell, WA4 days ago $31 - $34.22 per hour
Bristol Myers Squibb is seeking a Quality Assurance professional to maintain quality presence on the shop floor in Bothell, Washington. The role involves reviewing batch records and ensuring compliance with regulations. Candidates should hold a relevant degree and have ...SuggestedHourly pay- An established industry player is seeking a Quality Associate II to join their dynamic team in Bothell. This role is crucial in maintaining cGMP quality operations within a regulated environment, ensuring that products and processes meet stringent standards. The successful...SuggestedNight shift
- 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
- 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
- In a rapidly changing world, HUB advises businesses and individuals on how to prepare for the unexpected. As one of the worlds' largest insurance brokers, our focus is dedicated to providing our customers with the peace of mind that what matters most will be protected-...Local areaFlexible hours
HUB International
Bothell, WA8 days ago $78k - $82k
...Job Title: QA Associate Location: Redmond, WA (onsite) Shifts: Days, Mon to Fri, 8 hour shifts, ending 16:00, with Ad-hoc days for business requirements. About Us: this is who we are At Just Evotec Biologics , we believe that curiosity is...Temporary workFlexible hoursShift workEvotec
Redmond, WA3 days ago- ...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...For contractorsImmediate start
$81k - $85k
HUB helps businesses and individuals prepare for unexpected events, offering advocacy and tailored insurance solutions that give clients control over what matters most. Opportunity This position is responsible for quality control to ensure broker standards are being met...Local area- 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...
- Evotec in Redmond, WA is seeking a QA Associate responsible for executing day-to-day quality assurance tasks in GMP manufacturing. You'll collaborate with various teams to ensure compliance with regulations and internal procedures. The ideal candidate has a Bachelor's...Flexible hours
$38.42 - $46.55 per hour
Bristol-Myers Squibb is hiring a QA Specialist for the Bothell location. The role ensures quality adherence within clinical and commercial cell therapy operations, serving as a subject matter expert in cGMP principles. Responsibilities include inspecting batch records,...Hourly pay- Quality Management System Administrator 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...
- Bristol Myers Squibb is hiring a QA Specialist to provide quality oversight for clinical and commercial cell therapy operations in Bothell, WA. The role requires 3-4 years of GxP experience and involves real-time review of batch records, ensuring compliance, and engaging...
- Bristol-Myers Squibb is hiring a Specialist - QA Shop Floor in Bothell, WA. This role provides quality oversight for clinical and commercial cell therapy operations, ensuring compliance with cGMP and other quality principles. You will collaborate with teams, perform real...Flexible hours
- An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP operations. In this role, you will be responsible for managing GMP records, ensuring compliance with regulatory standards, and facilitating the document approval...
- 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...
- An established industry player is seeking a Quality Assurance Document Control Associate Specialist to support cGMP Document Control operations. This role involves managing document change control processes, issuing batch records, and ensuring compliance with regulatory...
- An established industry player is seeking a QA Associate Specialist for Document Control to support cGMP operations at their Bothell site. This role involves managing an electronic document system, ensuring compliance with regulatory standards, and collaborating with cross...
- 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...
$87k - $95k
QA Specialist We are seeking a passionate and curious QA Specialist to join our team. In this role, you will drive impactful projects, collaborate with bright minds, and explore uncharted territories in GMP manufacturing. Responsibilities Review executed Manufacturing...Temporary workFlexible hoursShift work$87k - $95k
Evotec in Redmond is seeking a QA Specialist to manage quality assurance for GMP manufacturing. You will enhance QA systems and collaborate with various teams to ensure compliance. Qualified candidates should hold a bachelor's degree in a relevant field and have at least...Flexible hours$87k - $95k
Job Title QA Specialist Location Redmond, WA (onsite) Shifts Days 07:00 till 16:00, Tue to Sat or Sun to Thurs. Please confirm which shift works best for you. Overview As a QA Specialist at Just Evotec Biologics, you will handle day‑to‑day QA responsibilities for GMP...Temporary workFlexible hoursShift work- Evotec WD in Redmond, WA is seeking a passionate QA Specialist to enhance GMP manufacturing processes. In this role, you will review Manufacturing Batch Records, partner with teams to ensure compliance, and support quality monitoring programs. Ideal candidates should have...Flexible hours
- Quality Assurance Specialist At AdaptHealth we offer full-service home medical equipment products and services to empower patients to live their best lives out of the hospital and in their homes. We are actively recruiting in your area. If you are passionate about making...
- 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...
- A technology solutions provider based in Bellevue, WA, is looking for a Software Tester with a strong background in software testing. The ideal candidate will have over 3 years of experience, the ability to execute test scripts, debug issues across multiple network nodes...
$78k - $130k
...will approve investigations and change control activities to ensure compliance with configuration management policies. As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team...Permanent employmentLocal areaRelocation packageFlexible hours2 days per week- An established industry player is seeking a motivated Manufacturing Associate to join their dynamic team. This entry-level position offers an exciting opportunity to engage in manufacturing, testing, and packing of products while adhering to quality and safety standards...Afternoon shift
- An established industry player is seeking a talented Mechanical Engineer with a robust background in medical device product design. In this role, you will leverage your expertise to innovate and develop mechanical components while ensuring compliance with FDA standards....
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