ppJazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. /p h3Brief Description /h3 pPerform Quality Control activities in compliance with GMP and approved procedure covering the role of Scientist Quality Control in the Quality Control laboratories in Gentium Srl (Villa Guardia). /p h3Essential Functions/Responsibilities /h3 ul liPerform analytical quality control testing according to written instructions and executed and approved training plan. /li liPerform and support sampling of finished products, APIs, intermediates, starting material, raw materials, packaging components, in-process control and cleaning validation/verification samples according to approved instructions. /li liApply the procedures governing the QC and the site. /li liPromptly report to the line manager or QA any departure from standard processes and procedures, including out of specification test results. /li liReview analytical results. /li liIs responsible for the accuracy, traceability and integrity of the data generated during the execution of the test and procedures he/she has performed and contemporaneous data recording. /li liKeep the premises of the lab and relevant equipment in good status of cleaning and qualification according to approved instructions with specific reference to safety and quality aspects. /li liMake sure that equipment used for testing and stability of products are qualified according to approved procedures and perform qualification of equipment.



/li liMake sure that reagents and standards required for the execution of the analysis are available and within their expiry date including contemporaneous recording of information into the computerized systems. /li liMake sure that reagents, standards and samples are always clearly labelled and correctly stored according to approved procedure. /li liParticipate in the preparation of analytical validation and cleaning validation protocols and reports and stability studies protocols and reports. /li liParticipate in the investigation of quality deviation as required. /li liWrite, as applicable, QC lab instructions including but not limited to: SOPs, analytical method validation protocols/reports, equipment qualification protocols/reports, reference standard characterization, sampling instructions, stability protocol/report. /li liEmbrace the Continuous Improvements mindset by leveraging the Operational Excellence Culture and Tools in the day-to-day activities. /li liFor her/his Area of relevance/responsibility monitor and ensure compliance with the GMP and Quality System. /li liFollow Environmental, Health and Safety procedures in compliance with the principle of the company Policy; apply the relevant guidance and indications of the Integrated Management System. /li liAttend education and training courses in the Integrated Management System, GMP Quality, Procedures, Instructions, manuals and Operational Protocols. /li liPerform all work activities, in compliance with the safety directives, as required by Legislative Decree 81/08. /li liEnsure compliance with all applicable Laws, Codes, corporate standards and Procedures related to her/his area of relevance/responsibility, included the legislative decree 231/2001 and requirements of the Jazz Pharmaceuticals Code of Conduct. /li liStrictly observance and knowledge of Jazz Pharmacovigilance’s Policy. /li /ul h3Required Knowledge, Skills, And Abilities /h3 ul liKnowledge of compendial requirements (USP-NF, Ph. Eur., ICH guidelines).



/li liTwo or more years of experience in a Pharmaceutical Quality Control laboratory. /li liExperience in the execution of analytical method validation (protocol, execution, report). /li liExperience with qualification and maintenance of HPLC, UPLC, TOC, automatic titrators, major laboratory equipment. /li liAcquired/available experienced for the use of the following QC analytical software: Empower 3 CDS, Chromeleon, LabX, TiAMO, OpenLab. /li liExperienced for sampling/testing Cleaning Validation/Verification samples, APIs, raw materials. /li liDrafting and reviewing SOPs and technical documents both in Italian and in English /li liGood level of English written and spoken. /li liTeam building and capability of working in teams and on multiple projects. /li liExperience in 6S within QC laboratory. /li /ul h3Required/Preferred Education And Licenses /h3 ul liDegree in chemistry, CTF, biotechnology, biology /li /ul pJazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. /p pJazz Pharmaceuticals is committed to fair and equitable compensation. We provide total compensation packages that are market competitive. For this role, the base pay range is: €34,400.00 - €51,600.00. This range will be reviewed on a regular basis. /p pWithin this range, individual compensation will align to your qualifications, skills, relevant experience, job knowledge, and any other factors pertinent to the role. /p pWe ensure fair and competitive compensation aligned with your expertise and contributions, within our established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. /p pAt Jazz, base pay is only one part of total compensation. You may also be eligible for a discretionary annual cash bonus or incentive compensation (role dependent), in accordance with the terms of the Company's Global Cash Premio Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. /p /p #J-18808-Ljbffr

📌 Scientist Quality Control (Villa Guardia)
🏢 Jazz Pharmaceuticals
📍 Villa Guardia