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Process Engineer Solution Supply Specialist
Job Location:
Job Location:
Lucerne - Switzerland
Salary:
Not provided by the employer
Salary:
Posted:
3 September 2026 (Yesterday)
Posted:
Application Deadline:
1 December 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Process Engineer Solution Supply Specialist 12 months
(Weigh & Dispense Buffer & Media Prep). Onsite role.
Role Overview
You will act as a key link between direct floor operations and quality systems driving continuous improvement safety and compliance specifically within W&D and Solution Supply to support our upstream and downstream manufacturing streams.
Key Responsibilities
1. Technical Office Work Compliance & Deviation Management.
Quality & Document Control: Support the authoring revision and maintenance of SOPs sampling plans and departmental procedures to ensure compliance with GMP and GDocP requirements.
Digitization & MES: Support the onboarding testing training and execution of Manufacturing Execution Systems (MES / Electronic Batch Records).
Deviation & Risk Management: Lead investigate and escalate deviations occurring within Solution Supply. Act as a Quality Risk Assessment (QRA) and Change Champion.
Cross-Functional Collaboration: Lead and participate daily in cross-functional teams to collaboratively address and cover compliance quality and technical deliverables under direction.
2. On-the-Floor Operations (W&D & Solution Supply)
Weigh & Dispense (W&D): Perform routine operator activities within W&D raw material staging material transfers visual inspection and inventory control in strict adherence to GMP requirements.
Buffer & Media Preparation: Execute routine formulation sterile filtration and supply activities to provide critical buffers and media for USP and DSP processing.
Equipment & Cleanroom Operations: Operate set up and prepare process equipment.
Single-Use & Stainless Steel Systems: Assist with the assembly preparation and disassembly of single-use systems (SUS) (e.g. bags tubing filters) and traditional stainless steel formulation vessels.
Process Sampling: Execute critical process sampling (e.g. pH conductivity bioburden).
3. Safety Leadership & Culture
EHS Risk Assessments: Lead facilitate and participate in EHS risk assessments and site safety initiative implementations on-floor.
Continuous Learning: Help solve complex formulation and process problems.
Job Requirements
Education: Technical or scientific vocational training (e.g. Biotech/Chemical Laboratory Technician Chemical Operator Druggist/Pharmacist Assistant) or equivalent practical experience.
Experience: Min of 3 years of hands-on manufacturing experience within a GMP-regulated pharmaceutical environment (specifically in solution preparation formulation or central services).
Core Systems: Prior exposure to both paper-based batch records and electronic systems (e.g. MES EBR LIMS SAP).
GMP & Compliance: Strong practical understanding of Good Documentation Practices & ALCOA principles.
Equipment Expertise: Experience operating single-use systems parts washers autoclaves and analytical benchtop instruments (e.g. pH/conductivity meters).
Language Proficiency: Fluency in both German and English (written and spoken) is preferred.
(Weigh & Dispense Buffer & Media Prep). Onsite role.
Role Overview
You will act as a key link between direct floor operations and quality systems driving continuous improvement safety and compliance specifically within W&D and Solution Supply to support our upstream and downstream manufacturing streams.
Key Responsibilities
1. Technical Office Work Compliance & Deviation Management.
Quality & Document Control: Support the authoring revision and maintenance of SOPs sampling plans and departmental procedures to ensure compliance with GMP and GDocP requirements.
Digitization & MES: Support the onboarding testing training and execution of Manufacturing Execution Systems (MES / Electronic Batch Records).
Deviation & Risk Management: Lead investigate and escalate deviations occurring within Solution Supply. Act as a Quality Risk Assessment (QRA) and Change Champion.
Cross-Functional Collaboration: Lead and participate daily in cross-functional teams to collaboratively address and cover compliance quality and technical deliverables under direction.
2. On-the-Floor Operations (W&D & Solution Supply)
Weigh & Dispense (W&D): Perform routine operator activities within W&D raw material staging material transfers visual inspection and inventory control in strict adherence to GMP requirements.
Buffer & Media Preparation: Execute routine formulation sterile filtration and supply activities to provide critical buffers and media for USP and DSP processing.
Equipment & Cleanroom Operations: Operate set up and prepare process equipment.
Single-Use & Stainless Steel Systems: Assist with the assembly preparation and disassembly of single-use systems (SUS) (e.g. bags tubing filters) and traditional stainless steel formulation vessels.
Process Sampling: Execute critical process sampling (e.g. pH conductivity bioburden).
3. Safety Leadership & Culture
EHS Risk Assessments: Lead facilitate and participate in EHS risk assessments and site safety initiative implementations on-floor.
Continuous Learning: Help solve complex formulation and process problems.
Job Requirements
Education: Technical or scientific vocational training (e.g. Biotech/Chemical Laboratory Technician Chemical Operator Druggist/Pharmacist Assistant) or equivalent practical experience.
Experience: Min of 3 years of hands-on manufacturing experience within a GMP-regulated pharmaceutical environment (specifically in solution preparation formulation or central services).
Core Systems: Prior exposure to both paper-based batch records and electronic systems (e.g. MES EBR LIMS SAP).
GMP & Compliance: Strong practical understanding of Good Documentation Practices & ALCOA principles.
Equipment Expertise: Experience operating single-use systems parts washers autoclaves and analytical benchtop instruments (e.g. pH/conductivity meters).
Language Proficiency: Fluency in both German and English (written and spoken) is preferred.
About Company
Idibu
100 employees
Every business is now operating in an environment that’s susceptible to change. idibu has evolved against this changing backdrop. Whether driven by legislation, technology, customer demand or the economy, businesses now need to be agile and fleet of foot to ensure they can attr ... View more
