GMP QA Disposition Specialist — Quality Release & Docs
TechDigital Group
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 strong communication skills, an independent mindset, and the ability to multi-task effectively. Join a dynamic team that values continuous improvement and collaboration, where your contributions will directly impact the efficiency and productivity of the organization. If you thrive in a fast-paced environment and are passionate about quality assurance, this opportunity is perfect for you. #J-18808-Ljbffr TechDigital Group
- Ultimate.ai is seeking a Quality Senior Specialist Raw Material Disposition to support QC operations for late-stage and commercial biologics manufacturing in... ...consistency, and regulatory compliance of raw materials at our GMP facilities. The ideal candidate will have a Bachelor’...QualityFlexible hours
- ...Job Title: QA Associate Location: Bothell, WA*100% onsite... ...- Experience working in a GMP environment *Okay with candidates... ....* Maintains shop floor quality presence; disposition in-process materials and... ...in support of product release in accordance with specifications...Quality
- Evotec WD in Redmond, WA is seeking a passionate QA Specialist to enhance GMP manufacturing processes. In this role, you will review Manufacturing... ..., partner with teams to ensure compliance, and support quality monitoring programs. Ideal candidates should have a Bachelor...QualityFlexible hours
- ...Wednesday-Saturday The Quality Associate II position... ...directly supports Jump's release for infusion (RFI)... ...The primary focus of the QA Associate role will be... ...record review and product disposition is preferred. Strong computer... ...guidance during GMP events and initiation of...QualityShift work
$75k - $95k
Scorpion Therapeutics is seeking a Quality Assurance Senior Associate to support ongoing manufacturing at... ...facility in Bothell, WA. You will execute day-to-day QA tasks, review batch records, and ensure compliance with GMP standards. The ideal candidate will have at least...Quality$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...QualityFlexible hours- Evotec in Redmond, WA, seeks a Quality Senior Specialist Raw Material Disposition to support QC operations for biopharmaceutical manufacturing. This role is critical for ensuring regulatory compliance and quality of raw materials. Ideal candidates should have a Bachelor...QualityFlexible hours
- ...Job Title: Senior Specialist, Quality Assurance Location: Bothell... ...Quality Assurance (QA) Senior Specialist,... ...directly supports Jump's release for infusion (RFI)... ...the relation to product disposition Partners to assist... ...provide guidance during GMP events and initiation...QualityImmediate start
- 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...Quality
$92.4k - $126.5k
Job Title Quality Senior Specialist Raw Material Disposition - Quality Control (GMP) Location Redmond / Seattle, WA (Onsite) Shift Day... ...Responsibilities Compile lot release documentation for Product and... ...lot disposition meeting with QA, Manufacturing, QC, etc. Review...QualityTemporary workMonday to FridayShift workDay shift$92.4k - $126.5k
Job Title: Quality Senior Specialist Raw Material Disposition - Quality Control (GMP) Shifts: Day Shift, Monday-Friday, Core Hours 8:0... ...What You’ll Do Compile lot release documentation for Product and... ...lot disposition meeting with QA, Manufacturing, QC, etc. Review...QualityTemporary workMonday to FridayFlexible hoursShift workDay shift- ...Quality Assurance Document Control Associate Specialist Must Have List: 5+ years of experience with the following: Library Science, MS Office including Word... ...are not limited to receiving and reconciliation of GMP records, management of scanning, archival and retention...QualityContract workWeekend work
- 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...QualityFlexible hours
$75k - $95k
Quality Assurance Senior Associate (Onsite) Key Responsibilities Execute... ...Perform routine hands‑on QA activities (e.g., intake of incoming... ..., review, and approve lot disposition records Perform routine raw... ...Promote a culture of safety and GMP compliance Identify opportunities...QualityRemote workShift work- 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...Quality
- ...PURPOSE AND SCOPE OF POSITION: The Specialist is responsible for activities... ...cGMP in support of the QA Disposition group. Functional responsibilities... ...maintenance and review of quality records and manufacturing... ...Experience: B.S degree with 1-3 years GMP experience in the...QualityWork at office
- ...Quality Assurance Document Control (QADC) Associate Specialist Top skills: Strong communication and customer service skills... ...management of archival and retention of GMP records. Required... ...change requests, troubleshooting and releasing documents to an effective state....QualityLocal areaShift work
- 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...Quality
- An established industry player is seeking a Quality Assurance Specialist to enhance cGMP quality operations at their Bothell facility. This role... ...functional teams to drive improvements and support product releases, making a significant impact on both clinical and commercial...Quality
$92.4k - $126.5k
Job Title: Raw Material Quality Senior Specialist - Quality Control (GMP) Shifts: Day Shift, Monday-Friday, Core Hours 8:00am-5:30pm Location: Redmond, Seattle... ...of processes and systems to assure the quality of released raw materials. Provide communication as to the...QualityTemporary workWork at officeMonday to FridayFlexible hoursShift workDay shift- ...SCOPE OF POSITION* 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... ...software programs. Experience working in a GMP environment is preferred. Demonstrated success...QualityWork experience placementShift workNight shiftWeekend work
$75k - $95k
...clinical-stage biopharmaceutical company is seeking a highly motivated Quality Assurance Senior Associate in Bothell, WA. The role involves... ...7+ years of experience in relevant fields and familiarity with GMP biopharmaceutical operations. The position offers a salary range...Quality$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... ...you will handle day‑to‑day QA responsibilities for GMP manufacturing, build and enhance quality assurance systems, and collaborate with...QualityTemporary workFlexible hoursShift work$87k - $95k
QA Specialist We are seeking a passionate and curious QA Specialist to join our team. In this... ...minds, and explore uncharted territories in GMP manufacturing. Responsibilities Review... ...Execute process performance and product quality monitoring programs Alert senior...QualityTemporary workFlexible hoursShift work$87k - $95k
Job Title: QA Specialist Location: Redmond, WA (onsite) About Us At Just Evotec Biologics , we believe that... ...execution of day-to-day QA responsibilities for GMP manufacturing, along with building and enhancing the quality assurance systems. The role incumbent works...QualityTemporary workFlexible hoursShift work$78k - $130k
...do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our... ...Clinical and Commercial products for all regions Ensure post-release surveillance commitments are met, including participation in product...QualityPermanent employmentLocal areaRelocation packageFlexible hours2 days per week- ...ability to work effectively with others. Experience working in a GMP environment is preferred. The primary focus of the Quality Control Associate I role will be to support raw material testing and release within a cGMP environment. REQUIRED COMPETENCIES: Knowledge, Skills...Quality
- 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...Quality
- An established industry player is seeking a QA Associate Specialist for Document Control to support cGMP operations at their Bothell site. This... ...and collaborating with cross-functional teams to maintain quality documentation. The ideal candidate will possess strong communication...Quality
- ...Quality Assurance Specialist 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...QualityLocal areaFlexible hours
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