13.05.25 | Vollzeit | Visp | JobLeads GmbH | CHF 100’000 - CHF 125’000 In a related subject with a strong interest in working in the interdisciplinary environment of chemically modified biomolecules. In our team for preclinical development in bioconjugation, you are responsible for planning, monitoring, and managing projects for external customers as the project leader
Später ansehen12.05.25 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 Including automation systems. 3. Ensure manufacturing activities adhere to safety and quality standards, and are completed on schedule. 4. Manage processes or process units for clinical and commercial production of BioConjugates like ADCs. 5. Implement CQV strategies effectively in complex bioprocessing
Später ansehen02.05.25 | Vollzeit | Visp | JobLeads GmbH | CHF 100’000 - CHF 125’000 Of this great opportunity and apply now for the position as Principal Bioprocess Engineer DSP! What You’ll Do - Plan and manage operational activities in Upstream or Downstream Processing, including tech transfer support, material planning, document and batch record preparation, training, and deviation handling
Später ansehen29.04.25 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 Management and Engineering - IndustriesBusiness Consulting and Services and Biotechnology Research Referrals increase your chances of interviewing at Consultys Suisse by 2x Sign in to set job alerts for “Project Manager” roles. IT Project Manager Security - pharmaceutical environment Project Manager
Später ansehen24.04.25 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 Qualification, and validation (CQV) of equipment and processes in a GMP environment. 5. Strong knowledge of GMP regulations and biopharmaceutical manufacturing processes. 6. Proficiency in project management tools and methodologies. 7. Excellent problem-solving skills with the ability to manage technical
Später ansehen08.04.25 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 Etc. 6. Creation and timely implementation of training plans 7. Recognize, interpret and correct deviations 8. Comparison of cross-company process steps (relationships, dependencies, processes) 9. Administrative tasks such as managing shift handovers, inspections and creating instructions Key
Später ansehen05.04.25 | Vollzeit | Visp | JobLeads GmbH | CHF 100’000 - CHF 125’000 And optimization of current installations) for Visp. - Plan, direct and supervise the engineering and OT system maintenance activities within his team. - Building a successful team with a well-developed sense of commercial acumen combined with strong traditional project management & engineering skills. - Implement
Später ansehen29.03.25 | Vollzeit | Visp | JobLeads GmbH | CHF 100’000 - CHF 125’000 Experience in biopharmaceutical manufacturing with a focus on technical project management, GMP compliance, and process improvements. - Technical ExpertiseStrong knowledge and hands-on experience with GMP regulations, change management, commissioning, qualification (CQV), and validation of equipment
Später ansehen11.03.25 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 As it applies to equipment/facility validation. - Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s. Writing and/or revising procedures applicable to the Engineering activities. - Support the Engineering group to prepare the validation
Später ansehen01.02.25 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 In deviation reports processed in deviation reports QA activities follow legislation, authority and customer expectations. - Inform the Group Manager QA Qualification about relevant developments and trends. - Actively support the formulation and further development of qualification strategies and continue
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