Process Engineer
vor 1 Monat
As a member of the Manufacturing Technologies & Engineering group, the successful candidate will play a key role in implementing next-generation technologies to keep the company at the forefront of innovation in biologics development and clinical manufacturing.
General Information:
- Start date: ASAP
- Duration: 1 year
- Extension: possible
- Workplace: Lucerne
- Workload: 100%
- Home office:Â remote work is limited due to the projects and implementations led by the MT&E team
Tasks &Â Responsibilities:
Â- Supporting the introduction of novel and innovative solutions for biologics manufacturing within the facility
- Managing capital requests and sourcing activities
- Qualification of devices and equipment
- Authoring standard operating procedures
- Serving as a subject matter expert (SME) for newly implemented technologies and guiding their integration into routine production
- Authoring protocols and conducting design of experiments to demonstrate the comparability of new technologies with legacy systems
- Demonstrate excellent troubleshooting and problem-solving skills, as well as the ability to collaborate and work effectively within global and interdisciplinary teams
- Demonstrate a desire for continuous learning, improvement, and development, while approaching problems from new perspectives
- Providing support for the manufacturing of clinical supply drug substance, including resupply activities
- Operating equipment according to batch records, sampling plans, and standard operating procedures
- Collaborating with Facility Management and internal team members to ensure GMP compliance through routine monitoring, calibration, maintenance, and certifications of responsible equipment devices
Your Profile:
Â- A degree qualification in a relevant field (Science/Technical). An Advanced Degree (BSc or MSc) is desirable.
- At least 3 years of experience working in a relevant academic or industry field.
- Technical knowledge in biologics drug substance upstream operations, downstream operations, analytical testing, or process development.
- Detailed understanding of general principles of equipment qualification.
- Experience in cGMP in a sterile, vaccine, bulk, or finished goods pharmaceutical environment.
- Knowledge of design and operation of automated systems, such as DeltaV.
- Project management knowledge.
- Proficient verbal and written communication skills in English (B2). Proficiency in German (B1) is desirable.
- Ability to think logically and be proactive under pressure.
- Ability to work effectively as part of a team and independently.
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