Quality Assurance Specialist

Quality Assurance Specialist
Voir toutes les offres

Quality Assurance Specialist

Asia - Singapore
Ingénierie Industrielle et Life-Science
CDI
10/21/2024
POSTULER

Vos responsabilités

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Perform detailed reviews of raw materials, intermediate products, and finished products for compliance with quality specifications.
  • Manage the release process by ensuring all quality checks are completed before approving materials and products for use or distribution.
  • Ensure that all batch records and associated documentation are reviewed and meet regulatory requirements before product release.
  • Provide on-site quality oversight during the manufacturing process, ensuring that all operations comply with Good Manufacturing Practices (GMP) and company quality standards.
  • Collaborate with manufacturing teams to address any quality-related issues that arise during production and ensure prompt resolution.
  • Conduct regular GEMBA (on-site workplace observation) and GMP (Good Manufacturing Practice) walk-throughs of the manufacturing floor to identify potential quality risks, ensure compliance, and promote a culture of continuous improvement.
  • Document findings from walk-throughs and collaborate with the relevant teams to implement corrective actions where necessary.
  • Review, revise, and approve Standard Operating Procedures (SOPs), forms, and Manufacturing Batch Records to ensure they are up to date and compliant with current regulations and company policies.
  • Ensure that all documentation aligns with current industry standards and best practices in pharmaceutical manufacturing.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Perform detailed reviews of raw materials, intermediate products, and finished products for compliance with quality specifications.
  • Manage the release process by ensuring all quality checks are completed before approving materials and products for use or distribution.
  • Ensure that all batch records and associated documentation are reviewed and meet regulatory requirements before product release.
  • Provide on-site quality oversight during the manufacturing process, ensuring that all operations comply with Good Manufacturing Practices (GMP) and company quality standards.
  • Collaborate with manufacturing teams to address any quality-related issues that arise during production and ensure prompt resolution.
  • Conduct regular GEMBA (on-site workplace observation) and GMP (Good Manufacturing Practice) walk-throughs of the manufacturing floor to identify potential quality risks, ensure compliance, and promote a culture of continuous improvement.
  • Document findings from walk-throughs and collaborate with the relevant teams to implement corrective actions where necessary.
  • Review, revise, and approve Standard Operating Procedures (SOPs), forms, and Manufacturing Batch Records to ensure they are up to date and compliant with current regulations and company policies.
  • Ensure that all documentation aligns with current industry standards and best practices in pharmaceutical manufacturing.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients

Votre profil

This is some text inside of a div block.

Job Requirements:

  • Bachelor’s degree in Biotechnology, Pharmaceutical or related field
  • 3-5 years of experience in quality assurance within the pharmaceutical or biotechnology industry
  • Experience with product and raw material release processes and related documentation
  • Strong knowledge of GMP (Good Manufacturing Practices) and regulatory compliance
  • Hands-on experience in conducting GEMBA or GMP walk-throughs and identifying quality risks
  • Proficient in reviewing and approving procedures such as SOPs, forms, and batch records
  • Strong attention to detail and ability to work in a fast-paced, regulated environment
  • Excellent communication and collaboration skills to work with cross-functional teams
  • Good communication and problem-solving skills

À propos d'Antaes

Créée en 2007, Antaes est une société suisse de conseil en management et technologie classée dans le top 15 des sociétés de conseil en Suisse. Nous comptons plus de 300 ingénieurs expérimentés qui partagent notre passion.

 

Présents en Suisse, à Singapour, à Hong-Kong et en France, nous accompagnons nos clients suisses, et internationaux en intervenant dans les domaines suivants :

  • Conseil en organisation et transformation
  • Ingénierie Industrielle
  • Management des systèmes d'Information

 

En rejoignant nos équipes vous découvrirez :

  • Une équipe dynamique dans un esprit start-up
  • Un accompagnement humain et un suivi de l’évolution de votre carrière
  • Des challenges pour contribuer au développement de votre réseau
  • Des événements : team building, meet-up, workshop, Winter Event …
  • Une entreprise certifiée @HappyAtWork et ayant une politique RSE engagée (médaille d’or Ecovadis2023)

POSTULER
Nos autres offres

Quality Assurance Specialist

Asia - Singapore
CDI
Ingénierie Industrielle et Life-Science

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Perform detailed reviews of raw materials, intermediate products, and finished products for compliance with quality specifications.
  • Manage the release process by ensuring all quality checks are completed before approving materials and products for use or distribution.
  • Ensure that all batch records and associated documentation are reviewed and meet regulatory requirements before product release.
  • Provide on-site quality oversight during the manufacturing process, ensuring that all operations comply with Good Manufacturing Practices (GMP) and company quality standards.
  • Collaborate with manufacturing teams to address any quality-related issues that arise during production and ensure prompt resolution.
  • Conduct regular GEMBA (on-site workplace observation) and GMP (Good Manufacturing Practice) walk-throughs of the manufacturing floor to identify potential quality risks, ensure compliance, and promote a culture of continuous improvement.
  • Document findings from walk-throughs and collaborate with the relevant teams to implement corrective actions where necessary.
  • Review, revise, and approve Standard Operating Procedures (SOPs), forms, and Manufacturing Batch Records to ensure they are up to date and compliant with current regulations and company policies.
  • Ensure that all documentation aligns with current industry standards and best practices in pharmaceutical manufacturing.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients
Voir l'offre

Business Analyst F/H

Suisse - Genève
CDI
Digital et Systèmes d'Information

Dans le cadre d'un renforcement de l'équipe pour un projet bancaire stratégique, vous serez intégré(e) au sein d'une équipe projet. Votre mission principale sera de réaliser l'analyse fonctionnelle des processus existants, de définir les spécifications fonctionnelles et d'accompagner la mise en œuvre du projet.

 

En tant que Business Analyst F/H, vos missions seront :

 

  • Réaliser des analyses de l'existant sur les processus et les fonctionnalités des systèmes.
  • Définir et valider les spécifications fonctionnelles en collaboration avec les équipes projet.
  • Contribuer à la conception des schémas d'architecture technique et fonctionnelle.
  • Organiser et réaliser les tests usine et UAT, tout en assurant le support nécessaire.
  • Coordonner les acteurs du projet et assurer le suivi des développements, des corrections et du plan d’action.
  • Animer des workshops pour recueillir les besoins, valider les spécifications et préparer les comités de projet.
  • Participer aux Comités de Pilotage en rédigeant des comptes rendus et en préparant les supports.
  • Suivre la gestion budgétaire, y compris le suivi des factures.
  • Rédiger des procédures opérationnelles et assurer le contrôle des fichiers de tests et de migration.
Voir l'offre

Senior Business Analyst (Core Banking Operations)

Asia - Singapore
CDI
Digital et Systèmes d'Information

The Senior Business Analyst will perform the business analysis activities related to Core Banking platforms, Corporate actions processing, payments, and reconciliation systems of International Wealth Management activity in Europe and in Asia.

 

Job Description:

  • The Business Analyst works on banking projects including Core Banking Platforms, Corporate Actions, Settlements and Payments, and Reconciliation systems. Transversal topics involving other domains, with an impact on the Core Banking platform.
  • Proactively communicate and collaborate with external and internal third parties to analyze information needs and functional requirements and deliver the following artifacts as needed: Functional requirements, Business Requirements Documents, Use Cases, Screen and Interface designs, Business process designs
  • Define requirements using interviews, document analysis, requirements workshops, surveys, site visits, business process descriptions, use cases, scenarios, business analysis, tasks, and workflow analysis.
  • Drive and challenge business units on their assumptions of how they will successfully execute their plans
  • Strong analytical and product management skills required, including a thorough understanding of interpreting customer business needs and translating them into application and operational requirements.
  • Excellent verbal and written communication skills and the ability to interact professionally with a diverse group, of managers, subject matter experts, and technical teams.
  • Serves as the conduit between the customer community and the technology teams through which requirements flow.
  • Develop requirements specifications according to standard templates & methodology
  • Collaborate with the team’s experts to establish the technical vision and analyze tradeoffs between usability and performance needs.
  • Be the liaison between the business units, technology teams, and support teams
Voir l'offre

Ingénieur Informatique Industrielle F/H

Suisse - Genève
CDI
Ingénierie Industrielle et Life-Science

Nous recrutons en CDI un Ingénieur Informatique Industrielle (F/H) afin de rejoindre notre pôle d'expertise, dans le cadre d'un projet de grande envergure et longue durée, d'extension des activités de notre partenaire dans le canton de Neuchâtel.

 

En tant que Ingénieur Informatique Industrielle vos missions seront :

 

  • Concevoir, développer et maintenir des applications logicielles spécifiques aux machines industrielles en utilisant les langages de programmation tels que Python et C ++.
  • Collaborer avec les équipes d'ingénierie pour intégrer les logiciels aux machines spéciales, en assurant la compatibilité et la performance.
  • Conception d'automates pour les systèmes de contrôle des machines.
  • Collaborer à la mise en place et à l'amélioration des systèmes de gestion de l'exécution de la production (MES) pour optimiser la collecte de données et la traçabilité des processus.

 

Voir l'offre

Développeur d’applications 3D temps réel F/H

Suisse - Genève
CDI
Ingénierie Industrielle et Life-Science

Nous recherchons un Développeur d’applications 3D temps réel (H/F), dont la mission principale sera de développer des outils et bibliothèques utilisés pour la production d’applications 3D en temps réel, dédiées au desktop. Vous travaillerez en étroite collaboration avec plusieurs équipes, dans un environnement stimulant, pour développer des solutions adaptées aux besoins de notre client.

 

En tant que Développeur d’applications 3D temps réel F/H, vos missions seront :

 

  • Concevoir et développer des outils et bibliothèques pour la production d’applications 3D temps réel.
  • Assurer l'intégration des assets 3D dans les applications pour garantir une performance optimale.
  • Optimiser le code existant et contribuer à la définition de l'architecture logicielle.
  • Animer les cérémonies SCRUM et gérer efficacement le backlog des projets.
Voir l'offre
FORMULAIRE DE CANDIDATURE
* champs obligatoires
En soumettant ce formulaire, vous reconnaissez avoir pris connaissance de la politique de confidentialité de notre site web qui inclut vos droits concernant vos données personnelles.
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

Quality Assurance Specialist

Asia - Singapore
Ingénierie Industrielle et Life-Science
CDI

Vos responsabilités

This is some text inside of a div block.

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Perform detailed reviews of raw materials, intermediate products, and finished products for compliance with quality specifications.
  • Manage the release process by ensuring all quality checks are completed before approving materials and products for use or distribution.
  • Ensure that all batch records and associated documentation are reviewed and meet regulatory requirements before product release.
  • Provide on-site quality oversight during the manufacturing process, ensuring that all operations comply with Good Manufacturing Practices (GMP) and company quality standards.
  • Collaborate with manufacturing teams to address any quality-related issues that arise during production and ensure prompt resolution.
  • Conduct regular GEMBA (on-site workplace observation) and GMP (Good Manufacturing Practice) walk-throughs of the manufacturing floor to identify potential quality risks, ensure compliance, and promote a culture of continuous improvement.
  • Document findings from walk-throughs and collaborate with the relevant teams to implement corrective actions where necessary.
  • Review, revise, and approve Standard Operating Procedures (SOPs), forms, and Manufacturing Batch Records to ensure they are up to date and compliant with current regulations and company policies.
  • Ensure that all documentation aligns with current industry standards and best practices in pharmaceutical manufacturing.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients

Votre profil

This is some text inside of a div block.

Job Requirements:

  • Bachelor’s degree in Biotechnology, Pharmaceutical or related field
  • 3-5 years of experience in quality assurance within the pharmaceutical or biotechnology industry
  • Experience with product and raw material release processes and related documentation
  • Strong knowledge of GMP (Good Manufacturing Practices) and regulatory compliance
  • Hands-on experience in conducting GEMBA or GMP walk-throughs and identifying quality risks
  • Proficient in reviewing and approving procedures such as SOPs, forms, and batch records
  • Strong attention to detail and ability to work in a fast-paced, regulated environment
  • Excellent communication and collaboration skills to work with cross-functional teams
  • Good communication and problem-solving skills
Our positions are open to people who have been recognized as disabled workers. T&S Group promotes diversity and equality in the workplace. All qualified M/F candidates are considered for employment on an equal basis.

À propos d'Antaes

Créée en 2007, Antaes est une société suisse de conseil en management et technologie classée dans le top 15 des sociétés de conseil en Suisse. Nous comptons plus de 300 ingénieurs expérimentés qui partagent notre passion.

 

Présents en Suisse, à Singapour, à Hong-Kong et en France, nous accompagnons nos clients suisses, et internationaux en intervenant dans les domaines suivants :

  • Conseil en organisation et transformation
  • Ingénierie Industrielle
  • Management des systèmes d'Information

 

En rejoignant nos équipes vous découvrirez :

  • Une équipe dynamique dans un esprit start-up
  • Un accompagnement humain et un suivi de l’évolution de votre carrière
  • Des challenges pour contribuer au développement de votre réseau
  • Des événements : team building, meet-up, workshop, Winter Event …
  • Une entreprise certifiée @HappyAtWork et ayant une politique RSE engagée (médaille d’or Ecovadis2023)