05 ago - Emilia-Romagna
Productlife Group
Specific activities and responsibilities: brExecution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment brPreparation of validation protocols, reports and related documentation. brknowledge of GMP regulations brEnsure compliance with GMP requirements and internal quality standards. brSupport change controls, deviations, CAPAs, and risk assessments related to validation. brCollaborate with clients cross-functional teams (QA, Production, Engineering, QC) to support validation projects. brMaintain validation documentation and ensure the validated state of equipment and processes. brdrafting SOPs brdrafting validation master plan brRequired experience: 3-4 years brRequired Education : Bachelor's degree in Engineering, Life Sciences, Chemistry, Pharmacy, or a related discipline brRequired Languages : English + Italian (fully professional/native level)brRequired technical skills: brOffice 365 (Word, Excel, PowerPoint, Outlook).
brExperience in qualification and commissioning brWriting Skills (Sentence Structure and Construction, Clarity and Effectiveness,)brExperience in drafting qualification protocols, reports, SOPs, and other GMP documentation. brGood understanding of GMP requirements and validation principles. brAdditional experience and/or skills: brAttention to detail brTeam working brProblem solving brGood Interpersonal skills brFlexibility and willingness to travel to client sites as required. brAnnual Compensation Range: EUR 34,000 - 39,000brThe compensation range indicated in this job posting represents an estimated range for the position. 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.
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