Senior Commissioning & Qualification Ingénieur Sisslerfeld (a), 100% — Bachem AG
- Lieu
- Stein AG
- Contrat
- full-time
- Publié
- Aujourd'hui
Vue d’ensemble du poste
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
Exigences principales
- 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
Processus de candidature
- 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!
Entreprise et contexte
- 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
Détails supplémentaires
- 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
Notes et contenu original
- 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
Questions sur cette offre
Quel salaire propose Bachem AG pour ce poste ?
Bachem AG indique CHF 99 500 - 151 000 bruts par an pour ce poste à Stein AG. Il s'agit du salaire publié dans l'annonce d'origine (ou, si l'employeur ne précise pas de montant, d'une estimation réaliste pour le rôle et le secteur) — le calculateur de ce site le convertit en net réel une fois l'impôt frontalier et les cotisations sociales appliqués.
Est-ce un poste à temps plein, et quel type de contrat propose Bachem AG ?
Cette offre est un poste en temps plein. Le type de contrat affiché ici provient directement de l'annonce originale de l'employeur ; confirmez toujours les horaires exacts, le préavis et la durée d'essai avec Bachem AG pendant le processus de candidature, ces détails pouvant varier même au sein de la même catégorie de contrat.
Ai-je besoin d'un permis de frontalier pour un poste dans le canton de Argovie ?
Les résidents UE/AELE domiciliés dans la zone frontalière du pays voisin du canton de Argovie peuvent demander un permis G ; l'employeur suisse le dépose auprès de l'office cantonal des migrations après signature du contrat. Les règles de zone frontalière et les délais varient selon le pays voisin et le canton — confirmez les détails auprès de l'office des migrations du canton de Argovie ou avec les RH pendant la candidature.
Comment postuler à ce poste chez Bachem AG ?
Utilisez le bouton « Postuler maintenant » sur cette page — il renvoie directement à l'annonce originale de Bachem AG sur careers.bachem.com, votre candidature arrive donc directement dans le système de suivi des candidatures de l'employeur. Frontaliere Ticino ne collecte ni ne transmet lui-même les candidatures.
