ph3Role Overview /h3pJoining Moderna means advancing mRNA science to transform medicine. As part of our international centre for analytical excellence in Madrid, you will work on a broad pipeline and build a career that makes a real difference for patients. In this laboratory‑based individual contributor role, you will perform cGMP QC testing supporting In Vitro Relative Protein Expression (IVRPE), release and stability testing, while contributing to method qualification, continuous improvement and operational excellence. /ph3Responsibilities /h3ulliPerform cGMP Quality Control Bioassay testing with a focus on In Vitro Relative Protein Expression (IVRPE), supporting release and stability programs. /liliSupport Method Qualification and Acquisition activities as required. /liliPerform routine analytical bioassay testing supporting Cell Biology, including ELISA methodologies. /liliExecute analytical testing accurately and in accordance with approved procedures and regulatory requirements. /liliPerform general laboratory support activities including reagent preparation, sample management, equipment maintenance, laboratory housekeeping, and ensuring laboratory readiness. /liliPerform LIMS (LabVantage) sample result entry and execute electronic assay forms within LIMS. /liliSupport stability programs through timely testing and documentation. /liliPerform data entry and contribute to data trending activities. /liliManage and maintain QC laboratory supplies and inventory. /liliAssist with troubleshooting analytical methods and laboratory equipment where required. /liliSupport investigations related to out‑of‑specification (OOS) results and other non‑conforming events. /liliParticipate in quality systems activities including investigations, deviations, change controls, and CAPAs. /liliWrite,



revise and maintain standard operating procedures (SOPs), protocols, technical reports and other controlled documentation. /liliComplete and maintain accurate cGMP documentation for all work performed. /liliExecute work precisely in accordance with SOPs, work instructions and other internal guiding documents. /liliFollow good documentation practices and data integrity requirements to ensure records are accurate, complete and inspection‑ready. /liliEnsure compliance with all applicable GxP regulations, internal policies and regulatory expectations. /liliEstablish and maintain a safe laboratory working environment while promoting a culture of quality, compliance and continuous improvement. /li /ulh3Basic Qualifications /h3ulliTechnical qualification (FP, ciclo superior) or degree in Cell Biology, Molecular Biology, Biochemistry or another relevant scientific discipline with at least two years’ experience. /liliMinimum two years’ experience in a quality control laboratory of a pharmaceutical company is preferred. /liliHands‑on experience with cell‑based assays and biological systems, cell culture, transfection, ELISA or other immunoassays. /liliWorking knowledge of relevant and current FDA, EU and ICH guidelines and regulations preferred. /liliAbility to collaborate effectively in a dynamic, cross‑functional matrix environment.



/liliAbility to efficiently prioritize and complete multiple projects and tasks in a fast‑paced environment. /liliWorking proficiency in English, minimum B2 level required. /li /ulh3Pay Benefits /h3ulliCompetitive healthcare, plus voluntary benefit programs to support your unique needs. /liliA holistic approach to well‑being with access to fitness, mindfulness and mental health support. /liliFamily building benefits, including fertility, adoption and surrogacy support. /liliGenerous paid time off, including vacation, bank holidays, volunteer days, sabbatical, general recharge days and a discretionary year‑end shutdown. /liliSavings and investments to help you plan for the future. /liliLocation‑specific perks and extras. /liliThe benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. /li /ulh3Equal Opportunity Disability Accommodation /h3pModerna is committed to equal opportunity in employment and non‑discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process or to perform the essential functions of the position should contact the Accommodations and Adjustments team at /p /p #J-18808-Ljbffr

📌 Quality Control Associate, Bioassay (Madrid)
🏢 Moderna Therapeutics
📍 Madrid