GMP Compliance Specialist
vor 2 Wochen
GxP Compliance Specialist – Quality Control Fenil-sur-Corsier, Switzerland – 6-Month Contract (with the possibility of extension) Job Description As a GxP Compliance Specialist – Quality Control, you will join the Global Analytical Development, Analytical Operations & QC organization in Fenil-sur-Corsier, Switzerland. In this role, you will serve as the QC compliance expert, supporting daily laboratory operations, ensuring adherence to GxP and data integrity standards, and driving continuous improvement across quality systems. You will collaborate closely with QC, QA, and cross-functional stakeholders to maintain inspection readiness, manage deviations, and uphold robust documentation and training frameworks. Key Responsibilities Quality & Compliance Support (QC Operations) Support QC teams in daily operations as the compliance subject matter expert. Manage, investigate, and close deviations, non-conformances, events, and related quality records in collaboration with SMEs. Contribute to data reviews ensuring compliance with established quality requirements and GxP expectations. Perform periodic reviews and ensure timely progression of deviations, change controls, CAPAs, and investigations. Maintain and improve the data integrity knowledge base, including DI risk assessments, action plans, and routine reporting to leadership. Documentation & Regulatory Alignment Author, review, approve, and maintain relevant SOPs, Work Instructions, and quality documentation. Contribute to the evaluation of regulatory/pharmacopoeia updates relevant to QC processes. Support audit preparation and directly interact with internal auditors and external regulatory agencies. Recommend and implement system, process, and procedural improvements within QC compliance activities. Training, Cross-Functional Collaboration & Continuous Improvement Serve as the key liaison with QA to resolve compliance issues and drive corrective actions. 3>Essential Skills 5–10 years of experience in QC, analytical, or quality/compliance roles within biotech, pharma, or other regulated GxP environments. Strong understanding of GLP/GMP and Quality System requirements (ICH, FDA, EMA). Hands‑on experience with deviations, CAPAs, change control, and quality documentation. Solid investigational and problem‑solving skills; ability to interpret complex situations and recommend effective solutions. Prior experience supporting audits and interactions with health authorities. Knowledge of data generation, data processing, and data quality principles. English fluency (B2+ required); French is an advantage. Preferred Experience Practical experience working in a QC laboratory setting. Familiarity with laboratory information systems (LIMS), digital QC tools, automation technologies, and lean methodologies. Experience driving or supporting data integrity programs. Additional Insights Start Date: ASAP Contract Duration: 6 months (with the possibility of extension) Location: Fenil-sur-Corsier, Switzerland Interested? Send your CV to Khanyi Mabena at k.mabena@panda-int.com, or contact directly at +41 44 551 44 07 to learn more. #J-18808-Ljbffr
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Quality Assurance Compliance Specialist
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Lausanne, Schweiz Planet Pharma VollzeitQA Compliance Specialist - DSP (3-Month Contract) | Lausanne, Switzerland. Seeking an experienced QA Compliance Specialist to support deviation management activities within a large-scale Downstream Processing (DSP) environment. This is a 3-month contract with the possibility of extension pending budget approval. Location Fully on-site preferred to ensure...
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DSP QA Compliance Specialist
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Lausanne, Schweiz Planet Pharma VollzeitA global pharma recruitment agency seeks an experienced QA Compliance Specialist for a 3-month contract in Lausanne, Switzerland. The ideal candidate will manage compliance deviations within Downstream Processing operations, ensuring alignment with GMP standards. Strong experience in deviation management, fluency in French and English, and familiarity with...
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Quality Assurance Compliance Specialist
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Lausanne, Schweiz Planet Pharma VollzeitDirect message the job poster from Planet Pharma Seeking an experienced QA Compliance Specialist to support deviation management activities within a large-scale Downstream Processing (DSP) environment. This is a 3-month contract with the possibility of extension pending budget approval. Location Fully on-site preferred to ensure efficiency and strong...
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GMP QA/QC Specialist — Impact Quality in Pharma
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Cleaning Validation Specialist
vor 1 Tag
Lausanne, Schweiz Hays VollzeitCleaning Validation Specialist (m/f/d) Freelance/temporary employment for a project Lausanne Start date: asap Reference number: /1 Diesen Job teilen oder drucken Responsibilities Provide operational support and technical expertise for cleaning validation activities (protocols, reports, CAPAs, investigations) Review, challenge, and approve validation...
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Lausanne, Schweiz AurigaVision AG VollzeitA leading pharmaceutical company based in Neuchatel seeks a Quality Control Laboratory Specialist. The role involves supporting compliance with cGMP regulations, conducting risk assessments, and driving continuous improvement initiatives within laboratories. Candidates should have at least 2 years of QC lab experience in pharma and be fluent in French and...
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Lausanne, Schweiz AurigaVision AG VollzeitQuality Control Laboratory Specialist – Compliance & Continuous Improvement – Healthcare Industry – French speaking (Ref. 2685) Join to apply for the Quality Control Laboratory Specialist – Compliance & Continuous Improvement – Healthcare Industry – French speaking (Ref. 2685) role at AurigaVision AG Direct message the job poster from...
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Lausanne, Waadt, Schweiz Axepta Vollzeit CHF 80'000 - CHF 120'000 pro JahrFor one of our clients, a growing international pharmaceutical company based near Lausanne we are looking for an Analytical Operations Senior Specialist-Pharmaceutical Industry (Small Molecules)This global position supports analytical and quality control activities performed by manufacturing partners and contract laboratories, in close collaboration with...
