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
$29.65 - $33.36 per hour
...routine and semi-routine QA Raw Materials... ..., and documentation review for GMP operations.... ...reviews documentation for batch disposition and batch record assembly. The... ...to manufactured drug product and drug substance to... ...production batch records and associated data for product...SuggestedFull timeWork at officeFlexible hours$24 - $45.5 per hour
...detail-oriented Quality Assurance (QA) Specialist to support... ...functional exposure in a fast-paced production setting. Key Responsibilities Review batch production records, laboratory results, and... ...GMP compliance Support batch disposition and release for raw materials,...SuggestedContract workTemporary work$60k - $85k
...ORIC’s clinical stage product candidates include (1)... ...the Quality Assurance Associate will support Technical... ...activities, providing review and disposition of manufacturing and testing records. The successful candidate... ...Quality Assurance (QA) Batch Record Review, Product...SuggestedFull timeContract work$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- ...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
...projects through quality assurance processes throughout the product lifecycle. Work Schedule: Monday-Friday, core hours 8:00am-4... ...peptide drug candidates. Responsibilities Pre- and post-execution batch record review Authoring and updating documents related to Material...Monday to Friday$70.3k - $75.93k
...supporting the Quality department with inspection, product or material release, document control, production monitoring... ...Duties and Responsibilities Perform product lot disposition by reviewing executed packaging records for completeness, accuracy, and compliance to GMP...Full timeFlexible hours$85k - $89k
.... 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- ...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...
- ...seeking a Quality Assurance Associate II to join our team. This... ...in scaling clinical production activities, ensuring compliance... ...The position will assist in batch record review, deviation investigations,... ...in batch record review and disposition for clinical product manufacturing...Work at office
- ...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
$23 - $35 per hour
...Quality Associate – San Diego Location: San Diego, CA... ...attention to detail keeps production running smoothly and... ...FAIRs and related records) Evaluate non-conforming... ...Reports (NCMRs) Determine disposition of non-conforming... ...Perform customer contract reviews to ensure compliance...Hourly payContract workFor contractorsLocal areaShift workAfternoon shift$30 - $33 per hour
...Diego is seeking a Senior Quality Assurance Associate to contribute significantly to product quality and regulatory compliance. In this... ..., the successful candidate will perform QA release processes, review Device History Records (DHRs), and manage training in an electronic...Hourly pay- ...Post-Market QA Specialist The Post-Market QA Specialist plays a key role in ensuring... ...Hologic's on-market molecular diagnostic products. The ideal candidate will be responsible... ...timely, accurate, and complete complaint records in the complaint management system May...
$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- ...programs through a focus on data review, investigations, and quality... ...writing, data analysis, and product quality oversight. While maintaining... ...Review QC data, laboratory records, and analytical results to... ...Collaborate cross-functionally with QA, Manufacturing, and external...Work at officeShift work
- 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...
- Sonara Inc. is seeking a Quality Associate for an on-site contract opportunity in San Diego, California. The successful candidate will inspect incoming materials for GMP production and assist with various packaging activities, ensuring compliance with FDA guidelines. Applicants...Contract work
$21.69 - $24.41 per hour
...future of PCI. Summary of objective: The QA Specialist I, ACM is a key member of the... ...Responsibilities include continuous oversight of drug product manufacturing operator performance and... ...risks. Capture detailed and objective records of events, interventions, and...Full timeFlexible hours$21.69 - $24.41 per hour
The QA Associate I at PCI Pharma Services in San Diego is responsible for compliance with Quality Assurance requirements and collaborative team efforts. Duties include cGMP documentation review, area line clearance operations, and providing QA oversight during manufacturing...Hourly pay$65k - $70k
Catalent, Inc. in San Diego is hiring a Quality Assurance Associate I, Analytical to ensure compliance with quality standards. The position... ..., preferably with HPLC. The successful candidate will review controlled documents and support various manufacturing activities...$21 - $25 per hour
...standards Conducts home visits to new clients to welcome and review the Welcome Packet Observes and evaluates Home Care Aides... ...organizes work effectively and ensures its completion Meets all productivity requirements Demonstrates team behavior and promotes a team...Work at officeMonday to FridayFlexible hours$120k - $150k
...activities, including data for Management Review and KPIs. Participate in internal,... ...control requirements. Strong understanding of record retention. Skills & Capabilities... ...communication skills. Honest, loyal, trustworthy disposition. Strong planning, organizational and...Work at officeWorldwide- ...device team paving the way in a very unique product line? The Quality Systems & Document... ...Manage supplier documentation, qualification records, and ongoing compliance files. Training... ...reports for leadership, audits, and management reviews. Customer Feedback Follow-Up — Track,...Local areaImmediate start
- ...supporting 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...Full time
$90k - $110k
...ICIMS-2026-10392 Job Function: QA & RA Job Type: Temporary... ...of responsibility, including product design, verification and validation... ...compliance, (i.e. management review support, regulatory audits). Assists... .... Good understanding of record retention. Computer literacy required...Temporary workWork at officeWorldwideShift work$50 - $75 per hour
...initiatives, the team is seeking an experienced QA/QC Documentation Specialist to support... ...requirements Key Responsibilities Review, manage, and maintain GMP laboratory... ...validation protocols, testing protocols, and associated QC records Support documentation activities...Hourly payContract work$30 - $37 per hour
...quality professional who excels at documentation review, compliance oversight, and supporting the release of high-quality products that meet regulatory standards. As a key... ...for manufacturing operations, ensuring batch records and supporting documentation are accurate,...Contract workTemporary work
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