21.09.24 | Vollzeit | Wallis | JobLeads GmbH | CHF 80’000 - CHF 100’000 Functional Responsibilities - Ensure compliance with the client's safety, quality, and code of conduct standards - Adhere to GMP standards for the production of Mammalian products and intermediates - Maintain GMP-compliant documentation of processes and tasks Project-Specific Responsibilities - Represent
Später ansehen19.09.24 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 Preparation, creation, change, optimization and control of production documentation (EBR in MES automation system, SOPs, etc.) accordance to local procedures Key requirements - Master’s Degree in Biotechnology, Biochemical Engineering, Biochemistry or related Life Science subject, or Bachelor’s holder
Später ansehen16.09.24 | Vollzeit | Visp | JobLeads GmbH | CHF 100’000 - CHF 125’000 And ecology standards. 8. Ensure the sharing and leveraging of best practices and expertise within Lonza’s engineering community. 9. Ensure the successful hand-over of the project to the user-team including the right level of training and correct documentation. Candidate Profile 1. Education Bachelor’s
Später ansehen10.09.24 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 You work according to quality guidelines and, in addition to practical laboratory work, also carry out the necessary administrative activities, such as documenting the results and creating work instructions. - At the same time, you support laboratory maintenance (equipment responsibility) and ensure
Später ansehen06.09.24 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 Job Responsibilities 1. Operates, calibrates, and maintains quality control equipment and machinery. 2. Tests and assesses random product samples to ensure minimum pre-defined standards are met. 3. Aggregates test data and documents results of testing. 4. Receives, stores, and completes appropriate
Später ansehen06.09.24 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 Responsibilities 1. Designing, testing and changing recipes (under change control) during the design, start-up, qualification and production phase. 2. Ensuring the cGMP-compliant documentation (eBR; SOP; operating regulations, etc.). 3. Constantly improving procedures and processes in compliance
Später ansehen06.09.24 | Vollzeit | Wallis | JobLeads GmbH | CHF 80’000 - CHF 100’000 Independent quality support to project teams. 7. Review and approve validation documents. Minimum Qualifications 1. Degree in Biology, Chemistry, Biotechnology, Life Science or other related field or experience in the field of pharmaceutical industry. 2. Previous experience in GMP regulated pharmaceutical
Später ansehen03.09.24 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 Operate, calibrate, and maintain quality control equipment and machinery. 2. Test and assess random product samples to ensure they meet predefined standards. 3. Aggregate test data and document testing results accurately. 4. Receive, store, and complete appropriate paperwork for samples submitted
Später ansehen30.08.24 | Vollzeit | Fully | JobLeads GmbH | CHF 150’000 - CHF 200’000 documentable success exceeding sales goals. - Strong prospecting, selling, and closing skills; proven ability to work independently and in a team environment. - Ability to balance and conduct sales efforts from your home office and in the field. - Quick learner that can apply knowledge quickly. - Positive
Später ansehen25.08.24 | Vollzeit | Visp | JobLeads GmbH | CHF 80’000 - CHF 100’000 With customers during tech transfer, campaign preparation, execution, and closure, including daily batch status reporting - Compile process-related deviations, change requests, campaign reports, CMC sections in filing documents, and validation reports - Mentor scientific and production staff, conduct process
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