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QA Operations Specialist II

Maravai LifeSciences
CompanyMaravai LifeSciences
CategoryEngineering
LocationSan Diego
RemoteOn-site (inferred)
EmploymentNot stated
LevelNot stated
SalaryNot stated by the employer
Posted21 Jul 2026
Last verified8 Aug 2026
SourceEmployer ATS (greenhouse)
Applications are handled by the employer, not by us.Apply on the employer's site →
Description
Who we are :  Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.   At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitableculture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai’s portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market.  Your next role as a Miracle Maker   Maravai LifeSciences is seeking a #MiracleMaker to join our Quality Assurance team as a QA Operations Specialist II . The QA Operations Specialist II is r esponsible for the maintenance and continuous improvement of the Quality Management System. Includes the review and approval of deviations, NCRs, CAPAs, supplier management, change controls, and controlled documentation management, etc.  Provides review and approval for products and new product development documentation. Tracks and reports on quality metrics. Ensures compliance with company policies and procedures and applicable domestic and international standards and regulations, including but not limited to ISO 9001:2015. How you will make an impact:   Responsible for reviewing and approving Quality Events ( e.g.  d iscovery events  and  CAPAs ) to ensure  appropriate investigations  are  completed  in  a timely manner .   Provide  oversight for  quality operations  training  program  and  conduct s  quality related training .     Conduct  quality investigations to assess root cause, corrections, corrective actions, preventive actions, and  monitor  effectiveness.  Use of quality tools, such as 5-Why's, FMEA's, DMAIC, Cause and Effect Diagrams, Process Mapping, etc.    Lead  cross-functional teams in risk identification and mitigation activities.    Review  and  approve  product documentation for disposition of finished goods.    Review  and approve  change control s  of materials, equipment, processes, and procedures in cluding  appropriate documentation .   Maintai n  the control of documents and records.   Assure  compliance with all in-house or external specifications to standards such as ISO or customer requirements.                                                                                                                                               Work  with various functions, including Manufacturing, QC, R&D, commercial, customer service, technical support, facilities, IT, etc. to continuously improve  Quality  Operations .   Lead  Quality improvement projects.    Identif y  quality issues / discrepancies and effectively  resolve  these  issues  within the organization.