Technical Author, R&D (a), 100%

Technical Author, R&D (a), 100% # Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. To drive our continuous organic growth, we are constantly looking for highly qualified specialists. To strengthen our team in R&D, we are looking for a dedicated Technical Author R&D (a), 100% for writing production-relevant GMP documents.   You enjoy working in a GMP-regulated environment and find pleasure in creating corresponding documents. You can quickly familiarize yourself with changing tasks and are characterized by flexibility in prioritizing your tasks. Due to your strong communication skills and structured as well as exact way of working, you find it easy to successfully coordinate and process cross-departmental tasks. You strive to complete the assigned orders on time, either independently or in a team depending on the situation, through your high sense of responsibility, thereby ensuring a delay-free production process.   Your tasks:   • You create, review and update documents such as manufacturing instructions, SOPs, process validation plans and reports for our active ingredient production. In doing so, you work closely with the corresponding production departments • You implement process optimizations with regard to quality and efficiency increases • You perform risk analyses of production processes • When creating deviation reports, you support our production departments and implement the resulting corrective and preventive measures in our documents • Through your constant, active cooperation in cross-departmental processes, you represent the interests of all sides at the interfaces between production, quality assurance, Regulatory Affairs and R&D • You ensure that internal and regulatory requirements as well as agreed customer wishes are implemented in the best possible way   Your profile:   • University degree Master and/or Doctorate with a focus on (chemistry, pharmacy or similar field), also suitable for career starters • German as a native language (mandatory) as well as excellent English skills • Mastery of common MS Office tools • Interest and pleasure in the creation of production-related GMP documents • Ability to present complex chemical processes and technical contexts in an understandable manner • Exact way of working • Ability to work independently or in a team depending on the situation  • Strong communication and coordination skills   Our offer:   • A dynamic and strongly growing work environment with internal development and further training opportunities • In-house daycare center (KITA) on the Bachem Campus Bubendorf • 60% coverage of pension fund contributions by Bachem AG as well as the possibility for supra-mandatory provision with our choice savings plan • Access to benefit platforms with discounts at external partners • Fresh, healthy and diverse food in our staff restaurant • Diverse free sports activities on the Bachem Campus   Would you like to drive innovation forward together with us?   Have we aroused your interest? Then we look forward to receiving your complete application documents via our application portal.   Learn more about the Bachem Group and let yourself be inspired by our inspiring work environment at our location in Bubendorf! At Bachem, you-ll find a diverse, multicultural team. The (a) in the job title stands for all. We welcome applications from all candidates. What matters are your skills and motivation-regardless of age, gender, background, religion, or sexual orientation. *Please note: unsolicited resumes from recruitment agencies will not be considered.* Share this job posting by email