Bracco Suisse SA

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    "description": "Job opening — QA Operations Specialist | Bracco Suisse SA | 1228 Plan-Les-Ouates.\n\nIn this role, you will be responsible for:\n\n• Take ownership of core responsibilities within your area of expertise\n• Collaborate with cross-functional teams to achieve shared goals\n• Maintain quality standards and adhere to internal processes\n\nWe are looking for someone with:\n\n• Relevant degree and professional experience\n• Strong communication and teamwork skills\n• Professional level of English\n\nBracco Suisse SA provides:\n\n• The opportunity to join a well-established and successful company with bright prospects and state-of-the-art manufacturing sites and production facilities\n• A great development perspective and the opportunity to bring and utilize your know-how and expertise\n• Competitive remuneration packages as well as first class benefits complete this offer\n• Competitive salary package\n• Flexible working arrangements\n\nApply now for this QA Operations Specialist position in 1228 Plan-Les-Ouates.",
    "datePosted": "2026-06-18",
    "validThrough": "2026-07-18",
    "employmentType": "FULL_TIME",
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    "title": "QA Operations Specialist",
    "description": "Vous cherchez un emploi de QA Operations Specialist a Plan-Les-Ouates ? Bracco Suisse SA recrute.\n\nBracco Suisse SA based in Geneva (Switzerland) is a company of the international Bracco Group (\nwww.bracco.com\n), a leader in contrast agents for medical imaging. Our\nManufacturing Site based in Geneva is\napproved and inspected by the most important Regulatory Agencies (FDA, Swissmedic, etc.) and produce a lyophilized contrast agent exported in several countries.For our manufacturing site based in Geneva (Switzerland) we are looking for a:\nQA Operations Specialist\nJob mission\nTo support Quality Assurance Operations activities at the Geneva Manufacturing Site. The role involves ensuring that operations are performed in compliance with current pharmaceutical GMP requirements (EU and US) as well as with the BRACCO Corporate Quality and HSE Management System.\nUnder the responsibility of the Quality Assurance Operations Manager, you will have to perform the following tasks:\nActivities\nBatch record review\n•\nReview production batch records\n•\nRelease incoming consumables\n•\nReview packaging batch records\nImprove, maintain and ensure a continuous improvement of the following local Quality Systems to ensure the quality of the product:\n•\nEnsure that activities related to the sterile production quality are conform with the company policies and Corporate Quality directives. Main contact in case of sterile production deviation,\n•\nLead and manage deviations, including those related to production, maintenance, packaging, and laboratory activities, by driving and coordinating investigations in collaboration with the relevant functions,\n•\nDefine, implement, and follow up on corrective and preventive actions (CAPA) within the scope of responsibility, ensuring timely execution and effectiveness in line with defined deadlines,\n•\nManage complaints investigation,\n•\nParticipate to the review and approval of the validation/qualification documentation related to sterile production area,\n•\nEnsure the creation, review, and timely update of QA Operations documents,\n•\nReview/approve for issuance of GMP documents related to production area (SOP’s, specifications protocols, reports..),\n•\nParticipate in and/or lead risk analyses, in collaboration with cross-functional teams,\n•\nParticipate to change control process,\n•\nAuditor in self-inspections and external audits (lead auditor if qualified),\n•\nSupport external audit, notified Bodies and Regulatory Authorities,\n•\nAudit trail review of GMP systems.\n•\nTraining for classified area\nCommunication\n•\nEvaluate any signal detection that may have a potential impact on product quality.\n•\nPromptly report any Quality Alert or issue to the Operations Quality Manager and the Quality Unit Manager and actively contribute to the resolution of significant quality issues.\nEnsure effective communication and collaboration with Sterile Production, Maintenance, Packaging, and other relevant functions to support product quality throughout its lifecycle.\nManagement\n•\nIndirect management of investigation teams.\nQualifications & Skills\n•\nUniversity degree in Pharmacy, Chemistry or Biochemistry\n•\nOver 5 years in Quality Management in Pharmaceutical Industry\n•\nSolid knowledge of cGMP, including Annex 1\n•\nExpertise in lyophilized products and aseptic process\n•\nIndirect Management in project or investigation\n•\nQuality commitment, flexibility, initiative and problem-solving skills.\n•\nTeam working; cross functional cooperation behavior.\n•\nFluency in French and English (both oral and written)\n•\nExcellent team player with a strong ability to communicate.\nWe offer\n•\nThe opportunity to join a well-established and successful company with bright prospects and state-of-the-art manufacturing sites and production facilities\n•\nA great development perspective and the opportunity to bring and utilize your know-how and expertise\n•\nCompetitive remuneration packages as well as first class benefits complete this offer\nIf you recognize yourself in this profile and are looking for a new challenge, send us your complete application (letter & CV) through this link\nSearch for Jobs\n\nCe poste est a pourvoir rapidement. Candidatez sans tarder.",
    "datePosted": "2026-06-15",
    "validThrough": "2026-07-15",
    "employmentType": "FULL_TIME",
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    "title": "PACKAGING MANAGER (M/F)",
    "description": "Bracco Suisse SA recrute un(e) PACKAGING MANAGER (M/F) a Plan-Les-Ouates.\n\nHeadquartered in Milan, Italy, Bracco Imaging is one of the world’s leading companies in the diagnostic imaging business. Bracco Imaging offers products and solutions for all key diagnostic imaging modalities: X-Ray Imaging (including Computed Tomography-CT), Magnetic Resonance Imaging (MRI), Ultrasound and Nuclear Medicine. For our Manufacturing Site based in Geneva (Plan-les-Ouates) and producing a lyophilized contrast agent exported in several countries, we are looking for a highly skilled professional as a\nPACKAGING MANAGER (M/F)\nYou will be responsible for organizing and supervising secondary and tertiary packaging operations, while ensuring compliance with EU and US cGMP standards as well as Health, Safety, and Environment (HSE) regulations.\nKey responsibilities:\n•\nTo organize and supervise secondary packaging activities\n•\nTo supervise maintenance program of secondary packaging equipment, with Maintenance and Engineering department (eg weekly TPM meeting)\n•\nTo operate and monitor equipment in accordance with established procedures - To check proper execution of cleaning activities related to secondary packaging areas\n•\nTo participate in the issuance of GMP documents related to the activities including, but not limited to, SOPs\n•\nTo participate in Regulatory inspections\n•\nTo approve new artworks for technical part\n•\nTo ensure that production records are fully evaluated and signed by an authorized person before batch production record review by the QA/QC Department\n•\nTo ensure that processes and production equipment are in an adequate state of validation and to participate in the initial and periodic qualification\n•\nTo manage and develop a team of 4 permanent employees, temporary colleagues in addition in case, fostering collaboration and team cohesion while ensuring performance and continuous skills development in line with departmental objectives\n•\nTo ensure that the required training of the department personnel is carried out and adapted according to the needs\nQualifications & Skills:\n•\nDegree in Pharmacy, Industrial Engineering, or related field\n•\n5 years’ experience in an industrial environment, preferably in the pharmaceutical sector, with strong expertise in packaging materials and processes\n•\nProven track record in driving operational excellence and continuous improvement (Lean, Six Sigma a plus)\n•\nStrong leadership and team management skills, able to motivate cross-functional teams\n•\nExcellent organizational, analytical, and problem-solving abilities\n•\nResults-driven, with background monitoring KPIs (OAE) and optimizing processes\n•\nFluent in French and English\nWe offer:\n•\nThe opportunity to join a well-established and successful company certified ISO 14001-45001 with bright prospects and state-of-the-art manufacturing site and production facilities.\n•\nA great development perspective and the opportunity to bring and utilize your know-how and expertise.\n•\nA benefit from the support of local and corporate management in making our production site a reference for the group. You will enjoy large autonomy in the daily management of your department.\nIf you recognize yourself in this profile and you want to take up a new challenge, apply by sending your complete application (cover letter & CV)\nclick here\n\nN'attendez pas -- envoyez votre candidature a Bracco Suisse SA aujourd'hui.",
    "datePosted": "2026-05-02",
    "validThrough": "2026-07-31",
    "employmentType": "FULL_TIME",
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    "title": "PACKAGING MANAGER (M/F)",
    "description": "Rejoignez Bracco Suisse SA en tant que PACKAGING MANAGER (M/F) a 1228 Plan-Les-Ouates.\n\nHeadquartered in Milan, Italy, Bracco Imaging is one of the world’s leading companies in the diagnostic imaging business. Bracco Imaging offers products and solutions for all key diagnostic imaging modalities: X-Ray Imaging (including Computed Tomography-CT), Magnetic Resonance Imaging (MRI), Ultrasound and Nuclear Medicine. For our Manufacturing Site based in Geneva (Plan-les-Ouates) and producing a lyophilized contrast agent exported in several countries, we are looking for a highly skilled professional as a\nPACKAGING MANAGER (M/F)\nYou will be responsible for organizing and supervising secondary and tertiary packaging operations, while ensuring compliance with EU and US cGMP standards as well as Health, Safety, and Environment (HSE) regulations.\nKey responsibilities:\n•\nTo organize and supervise secondary packaging activities\n•\nTo supervise maintenance program of secondary packaging equipment, with Maintenance and Engineering department (eg weekly TPM meeting)\n•\nTo operate and monitor equipment in accordance with established procedures - To check proper execution of cleaning activities related to secondary packaging areas\n•\nTo participate in the issuance of GMP documents related to the activities including, but not limited to, SOPs\n•\nTo participate in Regulatory inspections\n•\nTo approve new artworks for technical part\n•\nTo ensure that production records are fully evaluated and signed by an authorized person before batch production record review by the QA/QC Department\n•\nTo ensure that processes and production equipment are in an adequate state of validation and to participate in the initial and periodic qualification\n•\nTo manage and develop a team of 4 permanent employees, temporary colleagues in addition in case, fostering collaboration and team cohesion while ensuring performance and continuous skills development in line with departmental objectives\n•\nTo ensure that the required training of the department personnel is carried out and adapted according to the needs\nQualifications & Skills:\n•\nDegree in Pharmacy, Industrial Engineering, or related field\n•\n5 years’ experience in an industrial environment, preferably in the pharmaceutical sector, with strong expertise in packaging materials and processes\n•\nProven track record in driving operational excellence and continuous improvement (Lean, Six Sigma a plus)\n•\nStrong leadership and team management skills, able to motivate cross-functional teams\n•\nExcellent organizational, analytical, and problem-solving abilities\n•\nResults-driven, with experience monitoring KPIs (OAE) and optimizing processes\n•\nFluent in French and English\nWe offer:\n•\nThe opportunity to join a well-established and successful company certified ISO 14001-45001 with bright prospects and state-of-the-art manufacturing site and production facilities.\n•\nA great development perspective and the opportunity to bring and utilize your know-how and expertise.\n•\nA benefit from the support of local and corporate management in making our production site a reference for the group. You will enjoy large autonomy in the daily management of your department.\nIf you recognize yourself in this profile and you want to take up a new challenge, apply by sending your complete application (cover letter & CV)\nclick here\n\nPostulez des maintenant pour ce poste de PACKAGING MANAGER (M/F) a 1228 Plan-Les-Ouates.",
    "datePosted": "2026-04-29",
    "validThrough": "2026-07-28",
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