You manage daily manufacturing tasks and ensure operational readiness while maintaining compliance with regulations. Collaboration with teams and troubleshooting processes are essential aspects of this role.
Anforderungen
- •Bachelor Degree in Biotechnology preferred
- •3-5 years of successful experience
- •3-5 years in GMP relevant environment
- •Language: English or German
- •Willingness to learn
- •Hands-on mentality
- •Work on a shift rotation model
- •On-call duties encouraged
Deine Aufgaben
- •Support operational and inspection readiness.
- •Execute process and cleaning validation protocols.
- •Complete daily manufacturing activities for media and equipment preparation.
- •Log and report issues related to manufacturing activities.
- •Update progress in the shift handover file.
- •Advance shift issues to the shift lead.
- •Manage daily materials for media and equipment preparation.
- •Ensure compliance with GMP regulations and SOPs.
- •Troubleshoot cleaning and process recipes.
- •Collaborate with cross-functional teams for process improvements.
- •Raise deviations related to media and equipment preparation.
- •Work independently with a strong GMP mindset.
Original Beschreibung
# MBP Manufacturing Professional
**Lengnau, Switzerland** | **Full time** | **Fully Onsite**
**Work Schedule**
Rotational shift nights/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, No contact lens allowed; prescriptive glasses will be provided, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift
**Job Description**
Are you an experienced **Biotechnologist Operator** who thrives in an autonomous role? We are looking for a **Senior Biotechnologist Operator** to independently run and oversee bioprocess operations with minimal to no supervision. If so, we would love to hear from you!
**Your responsibilities**
* Support operational readiness and inspection readiness in Media, buffer and equipment preparation.
* Execute Process Validation and Cleaning validation protocols.
* Complete daily manufacturing activities in Media, buffer and equipment preparation, including equipment cleaning by CIP, COP or SIP.
* Report and log all issues with details related to manufacturing activities in the relevant systems.
* Complete assigned tasks and update progress in the shift handover file.
* Advance issues faced during the shift to the Shift lead or Team lead.
* Manage daily materials for Media, buffer and equipment preparation.
* Ensure compliance with GMP regulations and company SOPs.
* Troubleshoot cleaning and process recipes.
* Collaborate with cross-functional teams to drive process improvements.
* Raise deviations related to Media, buffer and equipment preparation.
* Working independently and having a strong GMP mindset and experience.
**Your qualifications:**
* Bachelor Degree in Biotechnology, Pharmaceutical, Food, or Chemistry is preferred, although equivalent experience will also be considered.
* 3-5 years of successful experience in pharmaceuticals or biotechnology operations.
* 3-5 years of experience working in a GMP relevant environment with a good understanding of GMP and GDP.
* Language: English or German.
* Willingness to learn.
* Hands-on mentality.
* Work on a shift rotation model, including regular weekend, public holiday, and night work (3-shift).
* On-call duties encouraged based on respective planning.