Associate Specialist Downstream Operations
As a member of the manufacturing team at our company, you will be responsible for supporting various activities related to the implementation and GMP manufacturing of early-phase clinical therapies.
Associate Specialist Downstream Operations
Prestigious pharmaceutical company
Stellenbeschreibung
Set up, practical execution and troubleshooting of downstream processes under Good Manufacturing Practices (GMP)
Knowledge of and compliance to GMP principles and EHS standards in the area of responsibility
Involvement in continuous improvement efforts and support for the implementation of new technologies, including non-GMP engineering runs or testing activities
Creation and updates of SOPs and (electronic) master batch records. Technical review of various documentation related to process transfer and GMP manufacturing
Material management using ERP systems (SAP)
Participation in sampling activities (including occasional weekend work) or on-call duties, as required by the process scheduling. Typical manufacturing activities do not include shift work.
Profil
Educational background in a relevant discipline
A minimum of 1-2 years of work experience in the pharmaceutical or biotech industry.
Ability to solve problems and take new perspectives on existing solutions with a desire to continuously learn, improve and develop.
Ability to perform under pressure in a complex GMP environment and assume responsibility. Flexible attitude when working with internal or external stakeholders to achieve ambitious targets.
Business Fluent in English and German:
Effective oral / written communication skills in German (C1)
Oral / written communication skills in English (B2+)
Residence within approximately 30 minutes commuting distance from Schachen (LU) or willingness to relocate
Driver's license (B) and access to a personal car to enable on-call duties
Das Angebot
Interested to support this project, during a peek phase?
Looking forward to your application jid53844d7ss jit0731ss jiy26ss
As a member of the manufacturing team at our company, you will be responsible for supporting various activities related to the implementation and GMP manufacturing of early-phase clinical therapies.
Associate Specialist Downstream Operations
Prestigious pharmaceutical company
Stellenbeschreibung
Set up, practical execution and troubleshooting of downstream processes under Good Manufacturing Practices (GMP)
Knowledge of and compliance to GMP principles and EHS standards in the area of responsibility
Involvement in continuous improvement efforts and support for the implementation of new technologies, including non-GMP engineering runs or testing activities
Creation and updates of SOPs and (electronic) master batch records. Technical review of various documentation related to process transfer and GMP manufacturing
Material management using ERP systems (SAP)
Participation in sampling activities (including occasional weekend work) or on-call duties, as required by the process scheduling. Typical manufacturing activities do not include shift work.
Profil
Educational background in a relevant discipline
A minimum of 1-2 years of work experience in the pharmaceutical or biotech industry.
Ability to solve problems and take new perspectives on existing solutions with a desire to continuously learn, improve and develop.
Ability to perform under pressure in a complex GMP environment and assume responsibility. Flexible attitude when working with internal or external stakeholders to achieve ambitious targets.
Business Fluent in English and German:
Effective oral / written communication skills in German (C1)
Oral / written communication skills in English (B2+)
Residence within approximately 30 minutes commuting distance from Schachen (LU) or willingness to relocate
Driver's license (B) and access to a personal car to enable on-call duties
Das Angebot
Interested to support this project, during a peek phase?
Looking forward to your application jid53844d7ss jit0731ss jiy26ss
Associate Specialist Downstream Operations Arbeitgeber: Michael Page
Michael Page ist ein hervorragender Arbeitgeber, der seinen Mitarbeitern in Zürich nicht nur ein attraktives Vergütungspaket bietet, sondern auch ein dynamisches und internationales Arbeitsumfeld, das die persönliche und berufliche Weiterentwicklung fördert. Die Unternehmenskultur legt großen Wert auf Teamarbeit und Vielfalt, was es den Mitarbeitern ermöglicht, ihre Fähigkeiten in der Vermögensverwaltung optimal einzubringen und zu erweitern, während sie bedeutende Beziehungen zu wohlhabenden Kunden aus der Golfregion aufbauen.
