Senior QA Specialist - Aseptic GMP & Batch Release
Kindeva Drug Delivery
Kindeva Drug Delivery is seeking a QA Specialist II to provide advanced quality oversight, lead investigations, and ensure timely product release. You will collaborate with cross‑functional teams to implement improvements and maintain regulatory compliance in a fast-paced manufacturing environment. The role requires experience with batch record review, GMP practices, and aseptic processing, with a focus on continuous improvement and data-driven decision making. #J-18808-Ljbffr Kindeva Drug Delivery
- Kindeva Drug Delivery is seeking a QA Specialist I/II to provide advanced quality oversight, evaluate batch documentation, and manage product disposition in a fast-paced... ...line clearance. This on-site role requires strong GMP knowledge and hands-on QA leadership. #J-18808-...Suggested
$95k - $124k
...paths as we move toward a common goal of elevating science and service for rare patients. Position Summary: The Senior Quality Assurance Associate - GMP/GDP Auditing is responsible for executing GMP and GDP audits, supporting supplier qualification, compliance oversight...SeniorContract workTemporary workRemote work- ...Impact You Will Make The QA Specialist I provides advanced... ...ensure timely product release. QA Specialist II partners... ...Responsibilities Evaluate and approve batch documentation, and use... ...and demonstrate aseptic techniques and behavior... ...in internal GMP audits and represent QA...SuggestedTemporary workLocal areaRemote workWeekend work
$75.5k - $84k
...Virginia and Maryland. Basic Function/Nature and Scope The Senior Quality Assurance Specialist provides quality input and oversight for GMP, GLP, and ISO 9001:2015 programs and projects under the direction of senior QA staff or management. The position audits programs,...SeniorFor subcontractorSeasonal workFlexible hours- ...Center seeks a Quality Assurance Associate to oversee QA and regulatory activities for the GMP/GTP facility at the Midwest Stem Cell Therapy Center. You... ...training records. The role involves document control, batch record review, internal audits, and investigation of deviations...SuggestedPart time
- ...Center is seeking a Quality Assurance Associate to perform QA and regulatory work for the GMP facility, ensuring FDA compliance and maintaining SOPs,... ...City campus. Under the Associate Director, you will support batch record review, deviations, CAPAs, training, and cross-...Part time
- ...hiring a Quality Assurance Specialist. The Quality Assurance... ...employee.The RolePerforms batch record review, product release, and dispositionDraft, review... ...development and maintenance of QA programs, procedures and... ...experience in a GMP environment or Associate's...Full timeContract workLocal area
- Role Summary The QA Specialist I provides quality oversight and compliance... ...and material preparation, aseptic compounding, filling, inspection... ..., SOP revisions, and batch documentation review. Identify... ...alignment. Participates in internal GMP audits and supports customer...Temporary workLocal areaRemote workWeekend work
- Kelly Science & Clinical is seeking a Senior Process Chemist for a 6-month contract in St. Louis, MO. The incumbent will lead development, scale-up, and transfer of API processes under GMP, collaborating with internal and external teams to ensure compliant, efficient manufacturing...SeniorContract work
- ...organization headquartered in Kansas City, MO, seeks a Senior Quality Assurance Specialist to oversee GMP, GLP, and ISO 9001:2015 programs. You will audit... ...deviations, CAPAs, and other quality events under senior QA guidance. The role requires a BS in a related science,...Senior
- Merck Animal Health in Desoto, Kansas, seeks a Fermentation Senior Operations Technician to join the Antigen Manufacturing Team. You will help scale up aseptic production, operate stainless-steel fermenters, and support downstream processes with a safety-first, quality-...Senior
- Clarivate is seeking an experienced Release Manager to join our Enterprise Applications & Data Services team in Philadelphia. You will coordinate... ...products and platforms, partnering with Product, Development, QA, DevOps, Infrastructure, Security and business stakeholders to...Senior
- Travere Therapeutics is seeking a Senior Quality Assurance Associate to lead GMP/GDP auditing across our external partner network. You will execute audits, support supplier qualification, and help maintain inspection readiness, ensuring compliance with FDA, EU, ICH, and...SeniorRemote job
- ...regulatory work as related to the operation of the GMP facility within the Midwest Stem Cell... ...(cGTPs 21 CFR 1271).* Responsible for QA aspects of clinical supply manufacturing,... ...operations.* Assists with document management and batch record review.* Perform and maintain...Hourly payPart timeWork experience placementLocal area
- Food expeditors inspect dishes for visual appeal and to ensure that food is properly prepared and served at the proper temperature in a timely fashion. Food expeditors are the link between the kitchen and the dining room and bar. Restaurants and kitchens of all types hire...Flexible hoursNight shiftAfternoon shift
- ...Commercial Manufacturing Quality Assurance Specialist to join our team. In this role, you will... ...support quality operations by reviewing batch records, ensuring compliance with FDA... ...RolePerform batch record review, product release, and disposition.Draft, review, and...Full timeLocal areaShift work
$230k - $295k
..., Compliance, and Operations to deliver growth-focused product releases and ecosystem partnerships that meet the highest bar for technical... ...an innovative infrastructure for money.Collaborating with senior product leadership and other product managers to align roadmaps...SeniorFlexible hours- ...adherence to company policies and regulatory guidelines (e.g., FDA, GMP). Planning and coordination of C&Q activities in line with a... ...knowledge in Biopharmaceutical Drug Substance Manufacturing and Aseptic Fill finish a distinct advantage. Demonstrated ability to work and...SeniorFor contractors
$109.62k - $126.79k
...Senior Systems EngineerSyms Strategic Group (SSG) is seeking a talented Senior Systems Engineer... ...processing rules, routing logic, and batch workflows. Analyze and resolve mapping... ...certificate/keystore configurations. Support release deployments, environment refreshes,...SeniorFull timeRemote work$30 per hour
...the propagation of mammalian cell culture, aseptic cell culture operations, execution of... ...manufacturing controls and calibrators, and complete batch records following cGMPs. Perform in-... ...Preferred: 6 months of experience in a GMP regulated environment. Preferred: 4-year STEM...SeniorContract workTemporary workWork experience placementFlexible hoursShift workRotating shift- ...Quality Specialist - Kansas City, KSQuality Specialist-Kansas City, KSThis is a full-time,... ...include but are not limited to: Formal Release, verification tasks, log updating and review... ..., including storage & disposal.Review batch paperwork and associated quality checks,...Hourly payFull timeWorldwideFlexible hoursShift work
- ...Onsite: Lenexa, KS Sr Auditor, QA We are currently seeking a... ...quality oversight of GMP/CMC activities supporting clinical... ...Serving as the Quality Assurance releasing authority for GMP/CMC... ...quality documentation, including batch records, deviations, investigations...SeniorFlexible hours
$20 - $24 per hour
Ranew's Companies is seeking a QA Specialist to join our team in Olathe, Kansas. You will inspect parts and equipment, read blueprints, and verify dimensions with calipers and rulers using MS Excel to document results. The role is full-time on first shift, offering a starting...Hourly payFull timeDay shift$83.3k - $138.8k
...patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you.The QA Compliance Specialist - Controlled Substances oversees quality and compliance activities related to the storage, handling, and distribution of...Full time$20 - $24 per hour
Now Hiring - QA Specialist Ranew's is seeking a QA Specialist to join our team in Olathe, KS. Job Description Location: Olathe, KS Salary: $20 - $24 /hour (starting pay is based on experience and shift) Job Type: Full-time (1st Shift) Benefits: Performance Bonus, Paid Holidays...Full timeImmediate startShift workDay shift- ...next step. We’re looking for a Quality Systems and Assurance Specialist to support our built-to-order bus and van manufacturing operation... ...materials, workmanship, and completed vehicles; prevent release until acceptance requirements are met. Partner directly with...Full timeWork at officeLocal areaRelocation packageMonday to Friday
- StoneX Group Inc. is seeking a seasoned Senior Specialist, PR & Communications to align with Commercial & Payments leadership and drive clear... ...& Payments narrative. You will manage end‑to‑end press release execution, build relationships with top-tier media, and report...Senior
$77k - $202k
...supply chain integration to support more effective operations.As a Senior Associate you will manage assigned workstreams, interpret... ...compliance workstreams that align with lifecycle, production, and release activities- Applying Lean Manufacturing, operations strategy,...SeniorFull timeH1bShift work- ...profile enablement, segmentation, audiences, and destinations.Guide batch, streaming, API, and event-driven integrations, including... ...have Experience with agile delivery, estimation, product roadmaps, release planning, and distributed teams.Compensation at Accenture varies...SeniorWork experience placementLive inWork at officeLocal area
- ENERCON is seeking a Structural Design Engineer to join our Nuclear Design Group. The role offers mid-level to principal opportunities with growth paths across disciplines, and may be FT, PT, or LTLB. Opportunities exist in Overland Park, KS among other locations. You will...Senior
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