For our client, a high-tech biotech company in the greater Lucerne area, we are looking for a motivated individual with strong project management experience and familiarity with upstream and downstream processes
Sr. Biotech Process Engineer (a)
As a member of the growing Biotech Process Engineering group, you will be responsible for the evaluation and implementation of novel equipment, innovative processes, and the implementation of next generation technologies to keep at the forefront of innovation in development and clinical manufacturing of biologics.
Your tasks
Senior Specialist Process Engineering:
* Coach team and support coordination of efforts with colleagues across the local site and global network in shaping and implementing next generation technologies and innovation for GMP Batch and Continuous Manufacturing in Drug Substance and Drug Product.
* Contribute tiered meeting structure coordinating activities locally and with international (US, Ireland) groups for implementation of new processes and technologies for Drug Substance manufacturing.
* A Change Champion within the organization and site, to bring about new technologies, digitization, and ways of working.
* Ability to solve problems and take new perspectives on existing solutions with a desire to continuously learn, improve and develop.
Act as an SME for the evaluation of innovative equipment for optimizing manufacturing processes, preparing user requirements and capital funding requests:
* Work to harmonize technologies in batch and continuous manufacturing, for easy flexibility in switching between the two paradigms.
* Implement and qualify new technologies / software / instruments that can simplify and reduce effort around GMP manufacturing and administrative processes.
* Support the development of GMP Documentation such as: Risk Assessments, Batch Records, Sampling Plans, Qualification Documents, and SOPs/WI's.
* Provide quality assurance and GMP compliance support within global and interdisciplinary teams.
* Aggregate process related knowledge and centralize for knowledge management.
Your qualifications
* University degree in Life Sciences, Natural Sciences or Engineering
* Minimum of 5 years of work experience in the pharmaceutical or biotech industry.
* Minimum of 3 years of experience with quality management and compliance systems, working knowledge of quality auditing
* Experience as a Project Manager with cross-functional team members
* Familiarity with Upstream and Downstream Unit Operations for biologics manufacturing
* Familiarity with Emerson DeltaV, SIPAT and the use of Automation in a manufacturing Process
* Detailed understanding of Critical Process Parameters, Critical Quality Attributes and general principles of equipment qualification
* Technical knowledge with Biologics drug substance operations and analytical testing or process development
* Competent in analyzing complex situations and showing practical problem-solving capabilities
* Business Fluent in English and German
Your application
Please apply online. For further information about the position, please contact your Gi Consultant, Mr. Nazim Sagkol (B. Eng.),
Gi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world. In Switzerland we operate with the brands Gi Life Sciences, Gi Group, Grafton and Bautech Personal. We are active in temporary, permanent and professional staffing as well as in a variety of complementary HR Services. With a direct presence in 40 locations across Switzerland and over 200 employees, we are one of the leading staffing companies in the Swiss recruitment market. Gi Life Sciences is specialist for Temporary and Permanent staffing in the Life Science sector, as well as a valuable partner for many other HR Solutions. We believe in experts talking to experts: all our professionals are certified in scientific sector, meaning that they are able to understand your needs and support you at 360°.