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Solutions Supply Specialist (a)

Luzern Interim View Job Description
For our client, an international biotech company in Lucerne area, we are looking for a Solution Supply Specialist (a). This role offers a perfect balance between technical office work (deviation management, SOP/MES authoring, and digitization) and active on-the-floor operations in Weigh & Dispense (W&D) and Buffer/Media Preparation. Start in October, for the next 12 months with extension option.

hinzugefügt 04/09/2026

  • International biotech company
  • 12 months contract with extension option

Firmenprofil

For our client, an international biotech company in Lucerne area, we are looking for a Solution Supply Specialist (a). This role offers a perfect balance between technical office work (deviation management, SOP/MES authoring, and digitization) and active on-the-floor operations in Weigh & Dispense (W&D) and Buffer/Media Preparation. Start in October, for the next 12 months with extension option.

Stellenbeschreibung

Key responsibilities include:

1. Technical Office Work, Compliance & Deviation Management

  • Quality & Document Control: Support the authoring, revision, and maintenance of Standard Operating Procedures (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) and align them with paper batch records to drive digitization in Solution Supply.
  • Deviation & Risk Management: Lead, investigate, and escalate deviations occurring within Solution Supply. Act as a Quality Risk Assessment (QRA) and Change Champion to drive compliance, process robustness, and operational optimization.
  • 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 and GDocP requirements.
  • Buffer & Media Preparation: Execute routine formulation, sterile filtration, and supply activities to provide critical buffers and media for Upstream (USP) and Downstream (DSP) processing.
  • Equipment & Cleanroom Operations: Operate, set up, and prepare process equipment in strict adherence to electronic/paper batch records and SOPs. Maintain the GMP status of formulation areas.
  • 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.
  • Equipment Upkeep & Prep: Support cleaning validation cycles, parts washing, autoclave operations (in compliance with validated cycles), calibration, and routine equipment maintenance.
  • Process Sampling: Execute critical process sampling (e.g., pH, conductivity, bioburden) in accordance with approved sampling plans and SOPs.
  • EHS Risk Assessments: Lead, facilitate, and participate in EHS risk assessments and site safety initiative implementations on-floor.

Anforderungsprofil

  • Technical or scientific vocational training (e.g., Biotech/Chemical Laboratory Technician, Chemical Operator, Druggist/Pharmacist Assistant) or equivalent practical experience.
  • 3+ years of hands-on manufacturing experience within a GMP-regulated biopharmaceutical or pharmaceutical environment (specifically in solution preparation, formulation, or central services).
  • 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 (GDP) and ALCOA+ principles.
  • Experience operating single-use systems, parts washers, autoclaves, and analytical benchtop instruments (e.g., pH/conductivity meters).
  • Proven ability to troubleshoot equipment/process issues and support deviation investigations to root cause.
  • Language Proficiency: Professional working proficiency in both German and English (written and spoken) is preferred
  • Cleanroom Readiness: Comfortable working in classified cleanroom environments (including gowning and physical handling of raw materials).

Sonstige Informationen

  • 12-month contract opportunity, gaining experience in a leading global biopharmaceutical manufacturing environment.
  • Varied role combining hands-on manufacturing operations in Weigh & Dispense and Solution Supply with technical projects, compliance activities, and MES digitization initiatives.
  • Professional development opportunity to expand expertise in GMP manufacturing, deviation management, quality systems, and cross-functional collaboration within biotech operations.



Referenznummer angeben
JN-092026-7096958

Zusammenfassung

Berufsfeld
Engineering & Produktion
Näheres Berufsfeld
Produktion, Fertigung
Branche
Healthcare / Pharmaceutical
Ort
Luzern
Vertragsart
Interim
Referenznummer
JN-092026-7096958

Die Michael Page verpflichtet sich zu Chancengleichheit, als Arbeitgeber genauso wie als Dienstleistungsunternehmen. Wir treffen Rekrutierungsentscheidungen ausschließlich basierend auf Erfahrungen und Fähigkeiten der Bewerberinnen und Bewerber. Diese Maxime gilt nicht nur für unsere Mitarbeiterinnen und Mitarbeiter, sondern auch für unsere Arbeit in der Recruiting-Branche.