Senior Commissioning & Qualification Ingegnere Sisslerfeld (a), 100% — Bachem AG
- Località
- Stein AG
- Contratto
- full-time
- Pubblicato
- Oggi
Panoramica
The Bachem Group is investing in a new site in Sisslerfeld in Northwestern Switzerland.
This step is part of the long-term strategy to expand production capacity by the end of the decade.
The new production site will play a central role in achieving these goals.
- The Bachem Group is investing in a new site in Sisslerfeld in Northwestern Switzerland.
- This step is part of the long-term strategy to expand production capacity by the end of the decade.
- Completed degree in engineering, natural sciences, or a related field
- At least 10 years of professional experience in the pharmaceutical or biopharmaceutical industry
Requisiti principali
- Completed degree in engineering, natural sciences, or a related field
- At least 10 years of professional experience in the pharmaceutical or biopharmaceutical industry
- Proven experience in international CAPEX projects (medium to large scale, complex requirements) Extensive C&Q expertise in areas such as: Biologics/Drug Substance, Drug Product Small Molecules
- Packaging, warehousing, GMP & non‑GMP infrastructure Automation systems & new technologies
- Strong knowledge of global regulations (FDA, EMA, ICH, ISPE Integrated Commissioning & Qualification, etc.) Ideally experience with KNEAT Gx
- Deep understanding of project management, PQS/EM compliance, and interfaces with Quality
- Excellent communication, collaboration, and leadership skills
- Analytical thinking and financial acumen to derive sustainable, efficient solutions
Processo di candidatura
- We look forward to receiving your complete application documents via our application portal.
- Learn more about the Bachem Group and get inspired by our exciting work environment!
Azienda e contesto
- The design phase of the project offers you unique opportunities to shape the future organization.
- We are looking for an experienced and dedicated Commissioning & Qualification (C&Q) Engineer (a) , 100% to support our global capital projects and play a key role in the standardization and further development of C&Q processes across our international network.
- In this role, you will be responsible for the successful planning, execution, and management of C&Q activities – from concept to handover – and will contribute your expertise to a wide range of projects worldwide. Your tasks:
- Leadership of C&Q activities within multidisciplinary large capital projects
- Coordination and management of C&Q‑related deviations and changes within defined timelines and in compliance with required quality standards
- Responsibility for budget, schedule, prioritization, resources, and the quality of C&Q execution
- Analysis of options, planning of execution strategies, and development of detailed C&Q schedules
- Preparation of tender documents, support in procurement processes, and cost estimation
- Ensuring a smooth handover to Operations and Quality
- Risk management, including the derivation of proactive measures in case of deviations
Dettagli ulteriori
- In this role, you will be responsible for the successful planning, execution, and management of C&Q activities – from concept to handover – and will contribute your expertise to a wide range of projects worldwide.
- Proven experience in international CAPEX projects (medium to large scale, complex requirements) Extensive C&Q expertise in areas such as: Biologics/Drug Substance, Drug Product
- Packaging, warehousing, GMP & non‑GMP infrastructure Automation systems & new technologies
- Strong knowledge of global regulations (FDA, EMA, ICH, ISPE Integrated Commissioning & Qualification, etc.) Ideally experience with KNEAT Gx
- Confident working style in global, culturally diverse teams
Note e contenuto originale
- Your tasks:
- Your profile:
- Proven experience in international CAPEX projects (medium to large scale, complex requirements)
- Extensive C&Q expertise in areas such as:
- Biologics/Drug Substance, Drug Product
- Small Molecules
- Packaging, warehousing, GMP & non‑GMP infrastructure
- Automation systems & new technologies
- Strong knowledge of global regulations (FDA, EMA, ICH, ISPE Integrated Commissioning & Qualification, etc.)
- Ideally experience with KNEAT Gx
Domande frequenti su questo annuncio
Che stipendio offre Bachem AG per questa posizione?
Bachem AG indica CHF 99'500 - 151'000 lordi annui per questo ruolo a Stein AG. Questo è lo stipendio pubblicato nell'annuncio originale (o, quando il datore non specifica una cifra, una stima realistica per ruolo e settore) — il calcolatore di questo sito lo converte nel netto reale una volta applicate imposta da frontaliere e contributi sociali.
È un ruolo a tempo pieno, e che tipo di contratto offre Bachem AG?
Questo annuncio è una posizione a tempo pieno. Il tipo di contratto mostrato qui arriva direttamente dall'annuncio originale del datore di lavoro; conferma sempre orario esatto, preavviso e durata del periodo di prova con Bachem AG durante il colloquio, perché questi dettagli possono variare anche all'interno della stessa categoria contrattuale.
Serve un permesso da frontaliere per un ruolo nel canton Argovia?
I residenti UE/AELS nella zona di frontiera del paese confinante con il canton Argovia possono richiedere il Permesso G; il datore di lavoro svizzero lo presenta all'ufficio della migrazione di quel canton dopo la firma del contratto. Regole sulla zona di frontiera e tempi di lavorazione variano per paese confinante e canton — verifica i dettagli con l'ufficio della migrazione del canton Argovia o con HR durante il colloquio.
Come mi candido a questa posizione presso Bachem AG?
Usa il pulsante "Candidati ora" in questa pagina — rimanda direttamente all'annuncio originale di Bachem AG su careers.bachem.com, quindi la tua candidatura arriva direttamente nel sistema di gestione candidature del datore di lavoro. Frontaliere Ticino non raccoglie né inoltra candidature in proprio.
