
Badra Mrabet
Farmaceutisch / Biotechnologie
Over Badra Mrabet:
Serious, dynamic, diplomate, passionate, positive and organized. I like teamwork that takes place according to schedules and I am always looking to improve and see in every change an opportunity to evaluate. |
Communication, organization and planning are my best assets.
Ervaring
| Professional experiences | Main tasks |
Advanced Consultant-Capgemini ingineering: 2020 – Takeda -- Data integrity Consultant |
Evaluation of manufacturing equipment data integrity and conduction according to Takeda applicable procedure assessments to several equipment as spectrophotometers, HVAC, palltronics, etc..
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2021 – Takeda -- Raw materiem &Incoming good inspection Coordinator :
| Support Receiving and Inspection activities of raw materials in order to ensure the product quality and the compliance to GMP, SOP’s, specifications and regulations. Treatment and finalization of aging deviations and CAPAs Assessment Change control and supplier notification impact on the receiving and inspection proces |
| 2022- JnJ – Project, transition & transformation & risk management PQR/CPV and Doc management- Currently | Weekly catch up meeting with JnJ for operational update Oversight over back office (Portugal & Morocco platforms) delivery pipeline Identification and follow up of actions to resolve pain points affecting service performance and value Managing blocking points for the Capgemini Eng. back office, including : -Centralizing and following up on access requests -Following up on IT issues raised by Capgemini back office users -Following up on issues/pain points raised by back office team to ensure prompt resolution -KPI follow up; RFT, OTD, approval on time, etc… -Support for operational meetings & communication (JnJ sites with Capgemini Eng. back office) -Operational meetings with JnJ site SPOC and Back office (workload vs. platform capacity/ hot topics) -ADM4 transformation (operational way of working harmonization) -Automation tool: Hands-on time efficiency gain data analysis -JIRA tool: follow up with back office team on implementation Monthly KPI extraction and consolidation with JnJ SPOC’s Bi monthly APR approval report provided to JnJ Sponsor Back office training completion follow Up Steering committee preparation, presentation and action plan follow up. Delivery and contract Management Supervise Commercial and Contract Management Use Capgemini Methods, Techniques and establish governance Control contract & scope Manage Client Expectations Extend client relationships Propose and discuss change requests Spot opportunities/Delivery Led sales Manage finances Manage Contribution Margin Manage finance KpIs Push accurate billing/On time payments Manage project reviews Develop team members |
Quality & Customer Support Manager and Investigation laboratory Manager at Sartorius Stedim- Bioprocess Solutions and Medical Device manufacturing Since 02/01/2015 | Representation of the quality policy and execution of the quality strategy with customers |
| Management of customer complaints from their openings until their closure | |
| Conduct quality indicators and conduct quality dashboards relating to customer complaints and feedback. | |
| Coordination of site audits; responsibility includes planning, preparation, training, supervision of external auditors and definition of action plans and follow-up of responses as well as audit indicators on the site. | |
| Definition and Implementing CAPAs and Effectiveness follow up and conduct CAPA indicators | |
| Team management, training and development | |
| Conduct activities ("crisis cell") related to customer; Ex: Risk analysis, quality crisis, materovigilance, product recall, contribution to "for cause" audits, etc. | |
Provides GMP/BPD training to all employees of the site. Provides Investigations, Root cause analysis, CAPA and technical writings. | |
| Contributes to compliance with the rules of Quality, Health, Safety and Environment, respecting the quality, hygiene, safety and environmental guidelines and by detecting anomalies, potential quality incidents or accident risks Security Environment | |
Quality Assurance Specialist in a pharmaceutical industry -INFOMED PHARMA 2013-2015 | Batch records review, investigation of quality events and CAPA implementation. |
| Documentation management | |
| Contributes to compliance with the rules of Quality, Health, Safety and Environment, respecting the quality, hygiene, safety and environmental guidelines and by detecting anomalies, potential quality incidents or accident risks Security Environment | |
| Education |
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| Main Training |
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Opleiding
----------------------- Skills
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Professionals uit dezelfde Farmaceutisch / Biotechnologie-sector als Badra Mrabet
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