Manufacturing Technologies

**Salary**:88 - 107'500 CHF gross per annum
- **REF Number**:00056717
- **Consultant**:Adrien Guimard
- **Contact**:0041 (0) 800 106 106
- **Date Published**:08.03.2024
- **Sector**:

- **Location**:Lucerne,
- **Discipline**:
QLS are recruiting for a Manufacturing Technologies & Engineering to join a project with a global Biopharmaceutical Company based in Lucerne on a contract basis for 1 year with option of an extension.

Company:
Main Responsibilities:

- Support introduction of novel, innovative solutions supporting the manufacture of biologics within the facility.
- Capital Requests and Sourcing
- Qualification of Devices / Equipment
- Authoring of batch records, sampling plans, and standard operating procedures.
- Act as SME for implemented new technologies, guiding the implementation into routine production.
- Author Protocols and Prepare Design of Experiments to show comparability of new technologies versus legacy
- Excellent trouble shooting and problem-solving skills as well as influencing, collaboration skills and teamworking ability to work with global and interdisciplinary teams.
- Ability to solve problems and take new perspectives on existing solutions with a desire to continuously learn, improve and develop.
- For novel and resupply of Continuous Manufacturing Clinical Supply Drug Substance.
- Support the day-to-day operations of batch and continuous manufacturing processes.
- Operate equipment according to batch records, sampling plans and standard operating procedures.
- Work with Facility Management / internal team members in the in the maintaining of GMP status of responsible equipment devices in routine monitoring, calibration, maintenance, and certifications.
- A degree qualification in a relevant field (Science/Technical). An Advanced Degree (BSc or MSc) qualification is desirable.
- A minimum of 3 years’ experience working in a relevant academic or industry field.
- Technical knowledge with Biologics drug substance upstream operations, downstream operations, analytical testing or process development.
- Verbal or spoken communication skills in German (B1) and/or English (B2).
- Knowledge of design and operation of automated systems such as Delta V.
- Ability to think logically and be proactive under pressure.
- Ability to work as part of a team and on own initiative in a constructive manner.
- cGMP experience in a sterile, vaccine, bulk or finished goods pharmaceutical environment
- Detailed understanding of Critical Process Parameters, Critical Quality Attributes and general principles of equipment qualificationApply:
Please could you send any correspondence in English Please quote job reference 56717 in all correspondence.

Adrien Guimard

**Senior Recruitment Consultant**

T: +41 (0) 800 106106