Quality Assurance jobs

Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #QA #QualityAssurance #Pharma #Validation #RiskAssesment #Autoclave - You have experience in quality assurance regarding validation in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. Our partner is looking for a QA Validation to join its team. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? As QA Validation, you will Provide QA support and oversight to validation activities according to validation procedures. * Ensure QA oversight in validation activities (IQOQ / PQ / PV…) * Review/Approve the validation documentation regarding the GMP requirements and the procedures * Ensure that production practices are aligned with validation conclusion Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #QA #QualityAssurance #Pharma #Validation #RiskAssesment #Autoclave - You have experience in quality assurance regarding validation in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. Our partner is looking for a QA Validation to join its team. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? As QA Validation, you will Provide QA support and oversight to validation activities according to validation procedures. * Ensure QA oversight in validation activities (IQOQ / PQ / PV…) * Review/Approve the validation documentation regarding the GMP requirements and the procedures * Ensure that production practices are aligned with validation conclusion
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In light of their further growth and professionalization of the Complaint Handling Process we are looking for a Senior Post Market Specialist EMEA, with a strong background in In Vitro Diagnostics. * 5 years of experience as Post Market Specialist, Complaint Handling Specialist or Regulatory Compliance in a manufacturing environment, preferably in in-vitro diagnostics * Providing training on the requirements related to Authority reporting, complaint handling process and Post Market Requirements to internal stakeholders * Supporting of the Post-Market Surveillance activities in alignment with regulatory requirements - Motmans & Partners * Tessenderlo * Contract duration unspecified * Full Time - Tosoh Corporation is part of a Japanese chemical and specialty products and materials group that comprises over 130 companies worldwide and a multiethnic workforce of more than 12,000 people. In light of their further growth and professionalization of the Complaint Handling Process we are looking for a Senior Post Market Specialist EMEA, with a strong background in In Vitro Diagnostics. * 5 years of experience as Post Market Specialist, Complaint Handling Specialist or Regulatory Compliance in a manufacturing environment, preferably in in-vitro diagnostics * Providing training on the requirements related to Authority reporting, complaint handling process and Post Market Requirements to internal stakeholders * Supporting of the Post-Market Surveillance activities in alignment with regulatory requirements - Motmans & Partners * Tessenderlo * Contract duration unspecified * Full Time - Tosoh Corporation is part of a Japanese chemical and specialty products and materials group that comprises over 130 companies worldwide and a multiethnic workforce of more than 12,000 people.
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Mechelen * Contract duration unspecified * Full Time - The Statistical Programmer in the field of R and SAS-programming and CDISC data standards and is foreseen as an active stakeholder that contributes to departmental strategic initiatives. Your responsibilities * with respect to the programming activities for clinical studies across therapeutic areas * Driving the design, development and delivery of efficient, flexible and modular code used for analysis and reporting and for submission. * Taking ownership of quality and timeline aspects of assignments related to programming deliverables while maintaining clear and effective communication amongst all internal and external parties involved in clinical studies and development programs. * Performing a hands-on role, but also coordinating the SAS programming activities performed by External Service Providers (ESP) Mechelen * Contract duration unspecified * Full Time - The Statistical Programmer in the field of R and SAS-programming and CDISC data standards and is foreseen as an active stakeholder that contributes to departmental strategic initiatives. Your responsibilities * with respect to the programming activities for clinical studies across therapeutic areas * Driving the design, development and delivery of efficient, flexible and modular code used for analysis and reporting and for submission. * Taking ownership of quality and timeline aspects of assignments related to programming deliverables while maintaining clear and effective communication amongst all internal and external parties involved in clinical studies and development programs. * Performing a hands-on role, but also coordinating the SAS programming activities performed by External Service Providers (ESP)
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As QA Manager, you will be part of a dynamic and international organisation, growing rapidly to meet the demands of the healthcare and pharmaceutical sector. * Defining and optimising EMVO's quality procedures, standards and specifications. * Monitoring and advising the performance of quality management systems. * Brussels * Contract duration unspecified * Full Time - Introduction - Passionate about preventing false medicines from reaching patients in Europe? Do you want to apply your QA and IT knowledge to a European, fast-paced environment? If these terms resonate with you, then we want to hear from you! Your responsibilities - You will be involved in successfully running an organisation which is critical to the European pharmaceutical supply chain and will be . * Implementing and maintaining the Document Management System via Veeva. As QA Manager, you will be part of a dynamic and international organisation, growing rapidly to meet the demands of the healthcare and pharmaceutical sector. * Defining and optimising EMVO's quality procedures, standards and specifications. * Monitoring and advising the performance of quality management systems. * Brussels * Contract duration unspecified * Full Time - Introduction - Passionate about preventing false medicines from reaching patients in Europe? Do you want to apply your QA and IT knowledge to a European, fast-paced environment? If these terms resonate with you, then we want to hear from you! Your responsibilities - You will be involved in successfully running an organisation which is critical to the European pharmaceutical supply chain and will be . * Implementing and maintaining the Document Management System via Veeva.
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Follow up of the advanced statement of the project * Write and/or review and/or approve project / production / qualification documentation * Certification in project management (e.g. PMI, Prince2) Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Implement an efficient DP manufacturing process * Stakeholder, communication and budget management * Define with local teams (prod, QA, Q&V, ENG, DEV, RA) the best qualification strategy (equipment and materials) * Coordinate the manufacturing activities of technical batches * Coordinate the manufacture activities of engineering / stability batches * Define with local teams (prod, QA, Q&V, ENG, DEV, RA) the best process validation strategy * Coordinate the manufacture of Media Fill Test and process validation batches * Coordinate the sampling and transfer of samples to each QC labs Follow up of the advanced statement of the project * Write and/or review and/or approve project / production / qualification documentation * Certification in project management (e.g. PMI, Prince2) Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - What are your responsibilities? * Implement an efficient DP manufacturing process * Stakeholder, communication and budget management * Define with local teams (prod, QA, Q&V, ENG, DEV, RA) the best qualification strategy (equipment and materials) * Coordinate the manufacturing activities of technical batches * Coordinate the manufacture activities of engineering / stability batches * Define with local teams (prod, QA, Q&V, ENG, DEV, RA) the best process validation strategy * Coordinate the manufacture of Media Fill Test and process validation batches * Coordinate the sampling and transfer of samples to each QC labs
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Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #QA #QualityAssurance #Pharma #Validation #RiskAssesment #Autoclave - You have experience in quality assurance regarding validation in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. Our partner is looking for a QA Validation to join its team. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? As QA Validation, you will Provide QA support and oversight to validation activities according to validation procedures. * Ensure QA oversight in validation activities (IQOQ / PQ / PV…) * Review/Approve the validation documentation regarding the GMP requirements and the procedures * Ensure that production practices are aligned with validation conclusion Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #QA #QualityAssurance #Pharma #Validation #RiskAssesment #Autoclave - You have experience in quality assurance regarding validation in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. Our partner is looking for a QA Validation to join its team. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? As QA Validation, you will Provide QA support and oversight to validation activities according to validation procedures. * Ensure QA oversight in validation activities (IQOQ / PQ / PV…) * Review/Approve the validation documentation regarding the GMP requirements and the procedures * Ensure that production practices are aligned with validation conclusion
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AW Europe is recognized and appreciated by the major automobile manufacturers for its culture of quality spearheading innovation and long-term partnership with its Customers. AW Europe is recognized and appreciated by most automobile manufacturers for its culture of quality spearheading innovation and long-term partnership with its Customers based on mutual trust. Based in our Quality Assurance Department in Braine-l'Alleud (South of Brussels), you will be part of a multi national team whose task is to make AWE the market leader for Quality and Customer Satisfaction for Automatic Transmissions. You will be the key Quality interface with your Customer(s) and liaise with various AW departments (such as Engineering, Manufacturing, Sales) across the world to ensure that the product quality meets Customer requirements. AW Europe is recognized and appreciated by the major automobile manufacturers for its culture of quality spearheading innovation and long-term partnership with its Customers. AW Europe is recognized and appreciated by most automobile manufacturers for its culture of quality spearheading innovation and long-term partnership with its Customers based on mutual trust. Based in our Quality Assurance Department in Braine-l'Alleud (South of Brussels), you will be part of a multi national team whose task is to make AWE the market leader for Quality and Customer Satisfaction for Automatic Transmissions. You will be the key Quality interface with your Customer(s) and liaise with various AW departments (such as Engineering, Manufacturing, Sales) across the world to ensure that the product quality meets Customer requirements.
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Add value to the business and ensure compliance by providing and coordinating logistic and general administrative support to the Belux GRA-I Team and the Head of Regulatory Affairs Belux, and by undertaking more specialized tasks and ad hoc project work which require an understanding of the regulatory activities and responsibilities of the team as well as an understanding of the regulatory requirements, internal standards and procedures, and working under minimal supervision. 5 years of experience in the field of administration, secretarial work or office/project management, with previous experience and preferably proven track record in a Regulatory Affairs environment, and/or experience in a related department (e.g. Clinical, Quality, Medical, etc) Assistant * Bachelor degree in Management/(Medical) Secretarial Assistant, Life Sciences or equivalent by experience. Pfizer SA * Brussels Add value to the business and ensure compliance by providing and coordinating logistic and general administrative support to the Belux GRA-I Team and the Head of Regulatory Affairs Belux, and by undertaking more specialized tasks and ad hoc project work which require an understanding of the regulatory activities and responsibilities of the team as well as an understanding of the regulatory requirements, internal standards and procedures, and working under minimal supervision. 5 years of experience in the field of administration, secretarial work or office/project management, with previous experience and preferably proven track record in a Regulatory Affairs environment, and/or experience in a related department (e.g. Clinical, Quality, Medical, etc) Assistant * Bachelor degree in Management/(Medical) Secretarial Assistant, Life Sciences or equivalent by experience. Pfizer SA * Brussels
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To strengthen our Quality Assurance Department of our Belgian facilities located in Braine-l'Alleud, we are looking for an experienced Quality Technics Specialist. As Quality Technics Specialist, you will be responsible for the Quality Technics activities, covering equipment, utilities, facilities qualification, change control and deviations handling, audits, in order to meet the PolyPeptide Quality Unit objectives and the regulations (GMP). * To write, implement and manage documentation related to quality technics activities in order to comply with the cGMP or other legislation, and with the PolyPeptide Quality System * To manage change controls and deviation reports applying to quality technics * To plan and prioritize qualification activities in close relationship with the Engineering planning, the production, the Quality Unit and the Supply Chain To strengthen our Quality Assurance Department of our Belgian facilities located in Braine-l'Alleud, we are looking for an experienced Quality Technics Specialist. As Quality Technics Specialist, you will be responsible for the Quality Technics activities, covering equipment, utilities, facilities qualification, change control and deviations handling, audits, in order to meet the PolyPeptide Quality Unit objectives and the regulations (GMP). * To write, implement and manage documentation related to quality technics activities in order to comply with the cGMP or other legislation, and with the PolyPeptide Quality System * To manage change controls and deviation reports applying to quality technics * To plan and prioritize qualification activities in close relationship with the Engineering planning, the production, the Quality Unit and the Supply Chain
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Our partner is looking for a Project Manager to join its team. As Project Manager, you will have a part of coordination and a part of documentation. You can handle different projects simultaneously owing to your organizational skills? Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - Contracting #ProjectManagement #TechnologiesTransfer #ProductionProcess #Vaccines #GMP - You have experience in production processes of vaccines in the pharma industry? You have an eye for details and you can resolve problem easily? Keep reading your future job description. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? * Transfer meetings with QA and QC * Follow up of action plan, minutes and reports * Ensure the proper execution of the planning * Making presentations * Reporting Our partner is looking for a Project Manager to join its team. As Project Manager, you will have a part of coordination and a part of documentation. You can handle different projects simultaneously owing to your organizational skills? Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - Contracting #ProjectManagement #TechnologiesTransfer #ProductionProcess #Vaccines #GMP - You have experience in production processes of vaccines in the pharma industry? You have an eye for details and you can resolve problem easily? Keep reading your future job description. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? * Transfer meetings with QA and QC * Follow up of action plan, minutes and reports * Ensure the proper execution of the planning * Making presentations * Reporting
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As Validation Technician, you will ensure the proper execution of equipment's Validation. Our partner is looking for a Validation Technician to join its team. You have experience in validation of QC equipment's in the pharma sector? * Manage the entire equipment lifecycle: purchasing, validation, maintenance and decommissioning * Maintain and execute a visual planning for the complete validation process follow-up, starting from the purchase approval - You have knowledge of QC equipment's validation in a GMP environment. You are knowledgeable about validation and QC equipment. Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #Pharma #Validation #GMP #QC #Equipment's #DataIntegrity - You have an eye for details and for work well done? Keep reading your future job description. As Validation Technician, you will ensure the proper execution of equipment's Validation. Our partner is looking for a Validation Technician to join its team. You have experience in validation of QC equipment's in the pharma sector? * Manage the entire equipment lifecycle: purchasing, validation, maintenance and decommissioning * Maintain and execute a visual planning for the complete validation process follow-up, starting from the purchase approval - You have knowledge of QC equipment's validation in a GMP environment. You are knowledgeable about validation and QC equipment. Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #Pharma #Validation #GMP #QC #Equipment's #DataIntegrity - You have an eye for details and for work well done? Keep reading your future job description.
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Our partner is looking for a Deviation Writer to join its team. As Deviation Writer, you will ensure Deviation Management. Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #Deviation #CAPA #Root-Causes #Investigations #Pharma #GMP - You have experience in Deviation management in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? * Management of deviations related to the activity in the building * Define Corrective Actions and Preventive Actions (CAPA) * Initiate and describe deviations in SAP * Investigate to identify root-causes * Propose adequate CAPAs * Follow the management of deviations * Closure of deviations within delay - Your profile - Who are you? Our partner is looking for a Deviation Writer to join its team. As Deviation Writer, you will ensure Deviation Management. Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #Deviation #CAPA #Root-Causes #Investigations #Pharma #GMP - You have experience in Deviation management in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? * Management of deviations related to the activity in the building * Define Corrective Actions and Preventive Actions (CAPA) * Initiate and describe deviations in SAP * Investigate to identify root-causes * Propose adequate CAPAs * Follow the management of deviations * Closure of deviations within delay - Your profile - Who are you?
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Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #QA #QualityAssurance #CSV #ComputerSystemValidation #pharma - You have experience in quality assurance regarding computer system validation in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. Our partner is looking for a QA CSV to join its team. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? As QA CSV, you will ensure Computer System work properly regarding regulations in place. * Writing, reviewing and approving of validation plans and validation summary reports * Writing, reviewing and approving of deviations & change control documentation * Reviewing and approving of IQOQ protocols & reports, etc. Experis * Walloon Brabant * Contract duration unspecified * Full Time - Your responsibilities - Walloon Brabant - contracting #QA #QualityAssurance #CSV #ComputerSystemValidation #pharma - You have experience in quality assurance regarding computer system validation in the pharma sector? You have an eye for details and for work well done? Keep reading your future job description. Our partner is looking for a QA CSV to join its team. This international company is well-known for its pharmaceuticals and vaccines. What are your responsibilities? As QA CSV, you will ensure Computer System work properly regarding regulations in place. * Writing, reviewing and approving of validation plans and validation summary reports * Writing, reviewing and approving of deviations & change control documentation * Reviewing and approving of IQOQ protocols & reports, etc.
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