QA Associate - Batch Records Review & Product Disposition
Travere Therapeutics
Travere Therapeutics in San Diego is hiring a Quality Associate to support Quality Operations, overseeing Manufacturing, Packaging, and Labeling. The role involves compliance support, audit program activities, and management of quality records. Ideal candidates should have 2-3 years of QA experience, strong interpersonal skills, and a thorough understanding of cGMPs. The position offers competitive pay, benefits, and a commitment to employee well-being. #J-18808-Ljbffr Travere Therapeutics
$85k - $105k
## Quality Associate, Batch Record Review and Product DispositionApplylocations: San Diegotime type: Full timeposted... ...Batch Record Review, Product Disposition, Clinical and Commercial Supplier Management... ...**:* Support Quality Assurance (QA) Batch Record Review, Product...SuggestedContract workTemporary workRemote workShift work- ...Therapeutics in San Diego is seeking a Quality Associate to support Quality Operations through oversight... ...technical operations and managing various quality records. The ideal candidate will have 2-3 years of experience in QA, strong problem-solving skills, and knowledge...Suggested
- ...30.41/hPurpose:The QA Complaint Intake Specialist... ...Complaint Triage Associate is responsible for... ..., and complaint records are prepared for... ...authorized channels. Review incoming complaint... ...description Device and product configuration... ...information Lot, serial, or batch number Patient...SuggestedWork at office
- ...processes, validation processes, product releases, document... ...attention to detail and record keeping skills. Perform batch release activities ensuring... ...verifications as needed. Review records for GMP... ...released product, product disposition, validation status, regulatory...Suggested
- ...events, supports product disposition and regulatory activities... ...oversight. The QA Specialist works... ...with the QA Associate and Sr. Quality Systems... ...assigned. Batch Release Own and... ...regulatory, or management review. Train and... ...Electronic Batch Record (EBR) capabilities...Suggested
$90k - $125k
...and manufacture your products to ensure we get... ...patient. The QA Operations Specialist... ...point of contact for Batch Disposition, Quality Control and Quality Record escalations and document review and approvals. Key... ...development of respective associates. $90,000 - $12...Work at officeLocal area- ...Inc. in San Diego is seeking a QA Operations Specialist to drive... ...will be the primary contact for Batch Disposition, Quality Control and Quality Records, collaborating with PMO and other... ..., supporting on‑the‑floor production, reviewing batch records, and guiding CAPAs...
- ...work plans. May be assisted by QA Specialists and Sr. Specialists.... ...inspection of incoming materials for GMP production • Assist with packaging floor... ..., line clearance, etc.) • Reviews production batch records, logbooks and other associated documents • Performs Quality...Contract workImmediate start
- ...CSD-JD-QA Associate – Clinical SuppliesThis is an on-site contract opportunity. Three months with potential extension. Under... ...compliance, auditing, label inspection, line clearance, etc.)Reviews production batch records, logbooks and other associated documentsPerforms Quality...Contract workImmediate start
$89.22k - $122.67k
...Investigations and CAPA's, change management, batch release and batch record reviews, site Quality audits and data... .... Identify procedural gaps and product risk and where appropriate, recommend... ...Willing to travel 10% - 25%. Relevant QA experience for 3-5 years in a 21 CFR...Temporary workLocal area- ...AssociateQuality Assurance Associate – Document Control... ...related quality records. The position is... ...procedures.The QA Associate works... ...routing documents for review and approval,... ...specifications, drawings, batch records, protocols... ...4 for combination products is desirable....
$100k - $118k
...process inspections, and real-time review of manufacturing activities and documentation. Support batch record review and verification of... ...inspections of finished drug product and related materials.... ...records, logbooks, forms, and associated documentation as authorized....Shift workNight shift$85k - $89k
...procedures. Responsible for implementing and maintaining quality assurance processes throughout the product lifecycle. Responsibilities Perform pre- and post‑execution batch record review. Author and update documents related to material management quality control, batch records,...Contract work- ...and design control processes, validation activities, product releases, document control and compliance efforts. Key duties include batch release support, line clearance coordination with manufacturing, GMP record review, and management of document changes and training...
$70.3k - $75.93k
...including document control, training administration, product and material release, production monitoring,... ...Responsibilities: Independently perform product lot disposition by reviewing executed packaging records for completeness, accuracy, and compliance with cGMP...Full timeContract workFlexible hours- ...the status of finished products produced Based on... ...technical skills and QA experience, anticipates... ...document generation and review Participates in CI projects... ...Support functions associated with the packaging of... ...drug material Perform batch record review Participates...
$95k - $124k
...The Senior Quality Assurance Associate – GMP/GDP Auditing is responsible... ..., and risk assessments. Review supplier responses and... ...quality metrics, and compliance records. Maintain supplier qualification... ...their potential impact on product quality, patient safety, and...Full timeContract workTemporary workRemote work$108.03k - $140k
...Tolerance Reports, and CAPA records, ensuring timely... ...quality meetings, represent QA in daily meetings, and... .... Additionally, they review and approve manufacturing... ..., and coordinate Product Quality Committee meeting... ...years of experience, an Associate’s degree with 6 years of...$60k - $70k
...global leaders in providing products and services within the... ...Assurance team as a QA Operations Specialist... ...Management System. Includes the review and approval of... ...with document and record control functions as needed... ...product documentation for disposition of finished goods....For contractorsWork at officeLocal area$95k - $124k
...The Senior Quality Assurance Associate - GMP/GDP Auditing is responsible... ..., and risk assessments.Review supplier responses and evaluate... ...quality metrics, and compliance records.Maintain supplier... ...assess their potential impact on product quality, patient safety, and...Contract workRemote work$60k - $70k
...global leaders in providing products and services within the... ...Assurance team as a QA Operations Specialist... ...Management System. Includes the review and approval of... ...documentation for disposition of finished goods. Review... ...control of documents and records. Assure compliance...Contract workFor contractorsFor subcontractorWork at officeLocal area- ...audits, and ensuring compliance with cGMP standards across manufacturing and operations. Key Responsibilities Review and approve batch records, deviations, and change controls in accordance with cGMP guidelines Support internal and external audits, including...
- ...Assurance Specialist in San Diego. The role independently owns defined QA processes, supports regulatory activities, and leads process... ...and Sr. Quality Systems Engineer. The ideal candidate will drive batch release, manage quality events, support FDA submissions, and...
- .... You will manage the eQMS, coordinate GMP training, and support audits and CI efforts. Responsibilities include reviewing packaging records for disposition, maintaining training and document control readiness, and leading internal, supplier, and regulatory audits. #J-...
- ...Job Description Job Description QA Documentation Specialist Location: San... ...to support the development, revision, and review of GMP manufacturing documentation. The ideal... ...to create and assemble clear, compliant batch records. Requirements Key Responsibilities...Full time
$25 - $31 per hour
...standards, procedures, and regulations (Monthly Internal Chart Audit Review (Medical and Dental) & Facility Site Visits, among others).... ...agencies or Health Management Organizations (Site Visits and Medical Record Reviews). Stay current with developments in quality management,...Remote workShift work- ...Job Description The Quality Assurance (QA) Specialist is responsible for ensuring compliance... ...process your private information, please review Insight Global's Workforce Privacy Policy:... ...chain quality oversight. Proven track record driving continuous improvement and quality...
- ...Biotherapeutics is seeking an Associate I, Quality Assurance - Operations... ...to support day-to-day QA activities at our San Diego locations... ..., label generation, and records management while ensuring GDP... ...preparation of metrics for leadership reviews. This position requires an...
- R&D Partners is seeking to hire a QA Complaint Intake Specialist in San Diego, CA . Your... ...calls, and other authorized channels. Review incoming complaint information and supporting... ...; ability to manage multiple complaint records within required timelines; and working knowledge...
$21 - $25 per hour
...standards Conducts home visits to new clients to welcome and review the Welcome Packet Observes and evaluates Home Care Aides in... ...organizes work effectively and ensures its completion Meets all productivity requirements Demonstrates team behavior and promotes a team-...Work at officeMonday to FridayFlexible hours
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