Process Expert DSP, Manufacturing Science and Technology 80 – 100 % (MSAT) (m/w/d)

With operations in 35+ nations and ~ 27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma , one of the world's largest collectors of human plasma, which is used to create CSL’s therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.

We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!

Process Expert DSP, Manufacturing Science and Technology 80 – 100 % (MSAT) (m/w/d)

We are seeking personalities with the desire and ambition to contribute actively to the commissioning and operation of the new production site in Lengnau. The position is situated in the Manufacturing Science and Technology (MSAT) team which aims to address scientific and technological questions of the drug substance manufacturing (USP, DSP, Buffer & Media) during the start-up and routine manufacturing in our new facility. The person in this role will mainly focus on DSP operations. Full-time working is clearly preferred, however part-time working represents an option for this position.

Main Responsibilities and Accountabilities:

During the Project Phase (until mid of 2021):

• Support definition of manufacturing processes for protein purification under the lead of the operational teams
• Both independently and collaboratively plan, prepare and guide through drug substance manufacturing process start-up activities
• Consult the operations teams in establishment of best cGMP practices and lean business processes, in close collaboration with the quality organization
• Contribute to the establishment of fully automated processes, together with stakeholders of the operation, engineering and automation teams
• Function effectively as a core team member

Qualifications and Experience

• Master / PhD degree preferred in chemistry, biochemistry, pharmaceutical, technical or life-science
• 3 – 5 years of experience in a cGMP-regulated production environment (pharmaceutical or biotech industry)
• Experience in a large scale, fully automated manufacturing environment preferred
• Knowledge of bioprocess unit operations and engineering scaling principles
• Learns new processes quickly and engages in assignments to drive for action
• Strong team player for collaboration in, and coordination of, task-dedicated, multi-disciplinary teams
• Strong communication skills, technical writing ability, and good attention to detail
• Good German and English proficiency (written and spoken)

Are you motivated to join us in this exciting journey to establish a state-of-the-art pharma manufacturing facility with most advanced technologies?

We are looking forward to receiving your online application. Applications must include a motivation letter and CV, as well as letters of references and copies of relevant transcripts and/or diplomas in the original language.

Please include all these in one document together with the CV.

Worker Type:

Employee

Worker Sub Type:

Regular