PAre you ready to join a strongworld leader /strong in the exciting and dynamic fields of thestrong Pharmaceutical and Medical Device industries? PQE Group /strong has been at the forefront of these industries strongsince 1998 /strong, with strong40 subsidiaries /strong and more than strong2000 employees in Europe, Asia and the Americas. /strong /ppbr/ppAs part of our ongoing growth and commitment to excellence, we are currently looking for a strongPVQA Support /strong professional to join our team. The role acts as a strongkey liaison between the Pharmacovigilance (PV) and Quality Assurance (QA) departments /strong, supporting routine quality activities, monitoring deviations, and ensuring timely and accurate documentation updates. /ppbr/ppuResponsibilities include, but are not limited to: /u /pullistrongPSMF Update: /strong Quality check of the Pharmacovigilance System Master File (PSMF) and preparation of sections related to quality, including strongindicators, audits, CAPAs, and deviations /strong. /lilistrongKPIs: /strong Preparation and production of strongmonthly indicator reports /strong. /lilistrongDeviations Management: /strong Follow-up on strongsupplier deviations /strong and management within internal systems. Monitor and supervise stronginternal deviations /strong, propose and track strongCAPAs /strong, and coordinate PSMF preparation activities. /liliServe as a stronglink between PV and QA departments /strong, facilitating communication and workflow. /liliEnsure proper use of the strongquality system platform /strong and adherence to established processes. /li /ulpbr/ppuRequired Qualifications: /u /pulliBachelor’s degree in strongPharmacy, Life Sciences, or related field /strong. /liliExperience in strongquality assurance, pharmacovigilance, or pharmaceutical operations /strong is preferred. /liliKnowledge of strongCAPA management, deviations, and quality metrics /strong. /liliStrong attention to strongdetail /strong and strongorganizational skills /strong. /liliExcellent strongcommunication skills /strong in English; Spanish fluency preferred. /liliAbility to strongcoordinate across departments /strong and work effectively with multiple stakeholders. /liliWillingness to receive strongtraining on quality systems and platforms /strong. /liliFamiliarity with pharmaceutical regulatory requirements is a plus. /li /ulpbr/ppstrongNext Steps /strong /ppUpon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. /ppIf there's a positive match, a technical interview with the Hiring Manager will be arranged. /ppIn the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. /ppAlternatively, if the outcome is negative, we will contact you to halt the recruitment process. /ppbr/ppstrongWorking at PQE Group /strong /ppAs a member of the PQE team, you will be part of a strongchallenging, multicultural company that values collaboration and innovation /strong. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. /ppIf you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. /ppApply now and take the first step towards an amazing future with us. /p