22 set - Gallicano Nel Lazio
Productlife Group
Descrizione dell’offerta di lavoroVuole candidarsi? Si assicuri che il suo CV sia aggiornato, poi legga attentamente le specifiche del lavoro prima di procedere.Specific activities and responsibilitiesExecution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment.Preparation of validation protocols, reports and related documentation.knowledge of GMP regulationsEnsure compliance with GMP requirements and internal quality standards.Support change controls, deviations, CAPAs, and risk assessments related to validation.Collaborate with clients cross-functional teams (QA, Production, Engineering, QC) to support validation projects.Maintain validation documentation and ensure the validated state of equipment and processes.drafting SOPsdrafting validation master planRequired experience1-2 yearsRequired EducationBachelor's degree in Engineering, Life Sciences, Chemistry, Pharmacy, or a related disciplineRequired LanguagesEnglish + Italian (fully professional/native level)Required technical skillsOffice 365 (Word,
Excel, PowerPoint, Outlook).Experience in qualification and commissioningWriting Skills (Sentence Structure and Construction, Clarity and Effectiveness,)Experience in drafting qualification protocols, reports, SOPs, and other GMP documentation.Good understanding of GMP requirements and validation principles.Additional experience and/or skillsAttention to detailTeam workingProblem solvingGood Interpersonal skillsFlexibility and willingness to travel to client sites as required.Annual Compensation Rangeup to EUR 30,000The compensation range indicated in this job posting represents an estimated range for the position. xysqume The final remuneration will be determined based on the selected candidate’s experience, skills, qualifications, and internal compensation policies, in accordance with applicable EU and local pay transparency and pay equity requirements.#J-18808-Ljbffr
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