Manufacturing Process Investigation Expert

Agap2 - HIQ Consulting AG

Agap2 - HIQ Consulting AG

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Infos sur l'emploi

  • Date de publication :

    22 avril 2024
  • Taux d'activité :

    100%
  • Type de contrat :

    Durée indéterminée
  • Lieu de travail :

    Bel-Air 1, 1003 Lausanne

Agap2 est un groupe européen d’ingénierie et de conseil opérationnel fondé en 2005 et spécialisé dans l’industrie. Nous travaillons dans les secteurs de la pharmacie, de la biotechnologie, des dispositifs médicaux, de l’horlogerie et de la mécanique de précision.

En tant que consultant, vous serez amené à accompagner nos clients dans la réalisation de leurs projets sur site en apportant votre expertise et vos compétences.

Vous êtes agile et désireux de vous adapter à différents environnements de travail qui alimenteront votre curiosité de voir ce qui se cache derrière les portes fermées des plus grands projets du portefeuille de nos clients.

Main duties & responsibilities:
The objective of this role is to manage deviations occurring in the various manufacturing units (USP and DSP) of one of our clients, for the different products within the quality system (i.e., Trackwise):

  • Conduct evaluations regarding the impact on the relevant equipment, products, or materials with the support of relevant experts.
  • Conduct deep-rooted investigations using Six Sigma methodologies (DMAIC, Ishikawa diagram, 5M, contradiction matrix, etc.), including the ability to collect and analyze data in various automated systems and on the field (regular GEMBA).
  • Identify and implement relevant corrective and preventive actions (CAPA), including preparing a business case and plan with relevant stakeholders.
  • Draft investigation and impact assessment reports in a comprehensive and scientific format.
  • Depending on the complexity of the discrepancy, lead a cross-functional investigation team including workshops or brainstorming sessions.

Required skills :
- Bachelor/Master in Engineering field (chemical, biotechnology) or equivalent experience
- 3-5 years of experience within a biotech/pharmaceutical GMP manufacturing environment (manufacturing, quality or support functions)
- USP background would be a plus instead of DSP (it is nice to have, not a must).
- Fluency French and excellent command of English (fluency is an asset)

Thank you for your interest in this opportunity. Please note that only candidates selected for a first exchange will be contacted.

The objective of this role is to manage discrepancies occurring in the various manufacturing units (USP and DSP) of one of our clients, for the different products within the quality system (i.e., Trackwise):

  • Conduct evaluations regarding the impact on the relevant equipment, products, or materials with the support of relevant experts.
  • Conduct deep-rooted investigations using Six Sigma methodologies (DMAIC, Ishikawa diagram, 5M, contradiction matrix, etc.), including the ability to collect and analyze data in various automated systems and on the field (regular GEMBA).
  • Identify and implement relevant corrective and preventive actions (CAPA), including preparing a business case and plan with relevant stakeholders.
  • Draft investigation and impact assessment reports in a comprehensive and scientific format.
  • Depending on the complexity of the discrepancy, lead a cross-functional investigation team including workshops or brainstorming sessions.

The objective of this role is to manage discrepancies occurring in the various manufacturing units (USP and DSP) of one of our clients, for the different products within the quality system (i.e., Trackwise):

  • Conduct evaluations regarding the impact on the relevant equipment, products, or materials with the support of relevant experts.
  • Conduct deep-rooted investigations using Six Sigma methodologies (DMAIC, Ishikawa diagram, 5M, contradiction matrix, etc.), including the ability to collect and analyze data in various automated systems and on the field (regular GEMBA).
  • Identify and implement relevant corrective and preventive actions (CAPA), including preparing a business case and plan with relevant stakeholders.
  • Draft investigation and impact assessment reports in a comprehensive and scientific format.
  • Depending on the complexity of the discrepancy, lead a cross-functional investigation team including workshops or brainstorming sessions.

The objective of this role is to manage discrepancies occurring in the various manufacturing units (USP and DSP) of one of our clients, for the different products within the quality system (i.e., Trackwise):

  • Conduct evaluations regarding the impact on the relevant equipment, products, or materials with the support of relevant experts.
  • Conduct deep-rooted investigations using Six Sigma methodologies (DMAIC, Ishikawa diagram, 5M, contradiction matrix, etc.), including the ability to collect and analyze data in various automated systems and on the field (regular GEMBA).
  • Identify and implement relevant corrective and preventive actions (CAPA), including preparing a business case and plan with relevant stakeholders.
  • Draft investigation and impact assessment reports in a comprehensive and scientific format.
  • Depending on the complexity of the discrepancy, lead a cross-functional investigation team including workshops or brainstorming sessions.

Contact

  • Solène Moehr
  • Agap2 - HIQ Consulting AG

Postuler rapidement