For one of our clients, an international pharmaceutical company based in canton Lucerne, we are seeking an Associate Specialist within the Downstream Operations group.
As a member of the manufacturing team at our client's company, you will be responsible for supporting various activities related to the implementation and GMP manufacturing of early-phase clinical therapies.
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Jobdetails
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Marta Tomczyk
randstad operational
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Jobdetails
General Information:
- Start date: ASAP
- Duration: 1 year
- Extension: possible (to be discussed)
- Contract type: temporary contract via Randstad (employment)
- Workplace: Schachen, Lucerne
- Home office: not possible, 100% onsite
- Workload: 100%
- Working hours: Standard with on-call duties
Tasks & Responsibilities:
- 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.
Your Profile:
- Educational background in a relevant discipline (e.g. Biotechnology)
- 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
- 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
Nice to have:
- Prior experience in the manufacturing of biologics under GMP, ideally including experience operating capturing and polishing chromatography, virus filtration, UFDF, formulation, fill & freeze
- Familiarity with the use of automated systems in manufacturing (DeltaV) and electronic batch records (PAS-X)
Sounds interesting? Apply now – we’re looking forward to receiving your applications!
For one of our clients, an international pharmaceutical company based in canton Lucerne, we are seeking an Associate Specialist within the Downstream Operations group.
As a member of the manufacturing team at our client's company, you will be responsible for supporting various activities related to the implementation and GMP manufacturing of early-phase clinical therapies.
General Information:
- Start date: ASAP
- Duration: 1 year
- Extension: possible (to be discussed)
- Contract type: temporary contract via Randstad (employment)
- Workplace: Schachen, Lucerne
- Home office: not possible, 100% onsite
- Workload: 100%
- Working hours: Standard with on-call duties
Tasks & Responsibilities: ...
- 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.
Your Profile:
- Educational background in a relevant discipline (e.g. Biotechnology)
- 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
- 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
Nice to have:
- Prior experience in the manufacturing of biologics under GMP, ideally including experience operating capturing and polishing chromatography, virus filtration, UFDF, formulation, fill & freeze
- Familiarity with the use of automated systems in manufacturing (DeltaV) and electronic batch records (PAS-X)
Sounds interesting? Apply now – we’re looking forward to receiving your applications!
