Technical Author — Bachem AG
- Lieu
- Vionnaz
- Contrat
- full-time
- Publié
- il y a 2 jours
Vue d’ensemble du poste
Bachem is a world leader in the development and manufacture of peptides and oligonucleotides for the pharmaceutical industry.
To strengthen our Technical Operations team in Vionnaz (Valais, Switzerland), we are looking for a Technical Author (all) 100% .
As a key member of TechOps, you will create and maintain GMP manufacturing documentation, support technology transfer and new product introduction projects, and ensure process knowledge is translated into compliant, manufacturing-ready records.
- Bachem is a world leader in the development and manufacture of peptides and oligonucleotides for the pharmaceutical industry.
- To strengthen our Technical Operations team in Vionnaz (Valais, Switzerland), we are looking for a Technical Author (all) 100% .
- Your key responsibilities
- Create, review, and maintain GMP documentation supporting manufacturing operations and technology transfer activities.
- Master's degree or PhD in Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or a related discipline.
- Strong scientific background with a solid understanding of chemical and pharmaceutical manufacturing processes.
Responsabilités principales
- Your key responsibilities
- Create, review, and maintain GMP documentation supporting manufacturing operations and technology transfer activities.
- Prepare Master Batch Production Records (MBPRs), manufacturing instructions, protocols, reports, and related technical documents.
- Translate process knowledge and development data into compliant, manufacturing-ready documentation.
- Collaborate closely with Process Scientists, laboratory teams, Manufacturing, and Quality Assurance.
- Support technology transfer projects from process familiarization through commercial implementation.
- Participate in new product introduction projects and manufacturing readiness activities.
- Ensure documentation complies with GMP requirements, internal procedures, and regulatory expectations.
- Contribute to the implementation of eMBPR and the standardization and digitalization of manufacturing documentation.
Exigences principales
- Master's degree or PhD in Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or a related discipline.
- Strong scientific background with a solid understanding of chemical and pharmaceutical manufacturing processes.
- Minimum 3 to 5 years of experience in a GMP-regulated pharmaceutical or chemical environment.
- Experience in technical writing, manufacturing documentation, technology transfer, or process development.
- Familiarity with batch record creation and document management systems.
- Excellent technical writing skills with strong attention to detail and a structured approach.
- Fluent in French and English (minimum C1 level).
- German is a strong asset.
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 at our location in Vionnaz.
Entreprise et contexte
- Proactive team player with strong organizational and communication skills; Our offer
- A modern and dynamic working environment within a fast-growing international company.
- Challenging projects of high scientific and technical value.
- Opportunities for professional development and continuing professional development. A corporate culture based on collaboration, innovation and excellence.
- Attractive working conditions and competitive employee benefits.
- Interested?
- Would you like to drive innovation together with us?
Détails supplémentaires
- Proactive team player with strong organizational and communication skills;
- Opportunities for professional development and continuing professional development. A corporate culture based on collaboration, innovation and excellence.
Notes et contenu original
- Your Profile
- Opportunities for professional development and continuing professional development.
- A corporate culture based on collaboration, innovation and excellence.
Questions sur cette offre
Quel salaire propose Bachem AG pour ce poste ?
Bachem AG indique CHF 71'000 - 107'500 bruts par an pour ce poste à Vionnaz. 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 Valais ?
Les résidents UE/AELE domiciliés dans la zone frontalière du pays voisin du canton de Valais 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 Valais 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.
