163 2022 canton of vaud English-speaking jobs in Visp

Step into a pivotal role at a global CMO and help shape the future of healthcare manufacturing. ... In this role, you will focus on ensuring the quality and safety of products within the Quality Control

And that’s the kind of work we want to be part of. ... The actual location of this job is in Visp, Switzerland. ... Ensure a cleaning validation overview of the plants and the corresponding products. ... What you'll do: Designing cleaning validation strategy, preparation of validation documents (study ... Responsibility for the cleaning validation assessment onchanges and deviations (approval of deviation

And that’s the kind of work we want to be part of. ... GMP experience and understanding of bioprocess technology. ... A couple of years working experience in biomanufacturing required. ... of therapeutic proteins from either mammalian (Bioprocess Engineer DSP). ... Excellent communication skills in English, good German skills of advantage.

You will reach your targets as you see fit and with the support of a practised team. ... Then we can offer you an exciting prospect: as part of the Swiss Life sales force, you can organise your ... shape their professional and personal development to their best advantage and throughout all phases of

And that’s the kind of work we want to be part of. ... Every day, Lonza’s products and services have a positive impact on millions of people. ... Key requirements: Graduate from a technical school (HF) / university of applied sciences (FH) or hold ... exciting chance to contribute to our dynamic environment, directly improving the quality and efficiency of ... People come to Lonza for the challenge and creativity of solving complex problems and developing new

this role, the Commissioning Qualification Validation (CQV) Engineer will be responsible for a range of ... tasks related to the validation of equipment and facilities within the pharmaceutical industry. ... activities, including: Facilities and utilities validation Validation life cycle management Execution of ... Project Duration: Approx. 9 Months Starting Date: ASAP Place of Work: Visp Key Responsibilities Engage ... The CQV Engineer will play a crucial role in maintaining the integrity of validation processes and documentation

Performing and sharing of lesson learned and evaluating areas of improvements. ... Tracking the writing or review of regulatory dossiers of our customers with the internal team. ... Initiating of invoices of executed Work Packages. Reporting completed revenues and revenue outlook. ... Organizing external kick-off and alignment with the scope of work. ... applications from all qualified candidates, regardless of background.

Facilitate the seamless onboarding of new team members, fostering a culture of quality and compliance ... Assist in the rollout of a new QMS, providing input from a user standpoint. ... Lead the development and ongoing management of the pharmaceutical quality system. ... Support the efficient handling of documents, deviations, CAPAs, and change requests. ... Full-time· Visp, Basel About Us ten23 health is a human-centric and sustainable strategic partner of

And that’s the kind of work we want to be part of. ... Conjugates (ADC) and other classes of Bio Conjugates. ... cGMP experience and a deep understanding of bioprocess technology. ... Proficiency in English is required; knowledge of German is an asset. ... Support the introduction of new equipment, especially for CAPEX projects.

And that’s the kind of work we want to be part of. ... We also recognize the value of every person’s contribution, regardless of characteristics, preferences ... Every day, Lonza’s products and services have a positive impact on millions of people. ... Serve as a subject matter expert in the design, commissioning, and qualification of new facilities, as ... Participate in the development and review of automation recipes for equipment and facility components

Minimum 5 years of experience in the pharma industry. ... Devices, Business Development Our client, a global market leader in the production and process support of ... We are recruiting CQV Engineers for an initial contract starting ASAP until the end of the year, with

* Proven work experience of the validation of laboratory, production equipment and knowledge of production ... operational phases of the site ... Associate (w/m/d) Location: Solothurn, Switzerland Duration: ASAP - 30/09/2025 + possibility of ... * Review and approval of Qualification, Validation and Engineering documents during both project and ... * Involvement in validation and change control of the BES systems being implemented and operated at

Description:Activities Executes manufacturing activities in the area of Drug Product according to cGMP ... Operating, setting up and cleaning production equipment and premises for the production of liquid and ... timely and with high quality the required production documentation (preparation, execution and review of ... process changes and CAPAs related to processes within required timelines Performs training activities of ... SOP execution Strong team orientation Effective communication skills and interaction with a variety of

Responsibilities: Plan and co-manage the execution of release analytics. ... is seeking a QC Associate to join the Bioanalytics Microbial Team, focusing on the release analytics of ... requires adherence to GMP and safety guidelines, with an emphasis on quality and timely completion of

Step into a pivotal role at a global CMO and help shape the future of healthcare manufacturing. ... Strong understanding of GMP and bioprocess technology. Fluent in English; German is a plus.

Language: Excellent command of English Strong analytical skills. ... CSV with strong experience in management of complex pharmaceutical projects. ... pharmaceutical company located in VISP we are looking for a CQV Lead: JOB DESCRIPTION Provide leadership of ... Strong knowledge of ISPE and ASTM guidelines with proven experience on large and complex projects. ... (bachelor level) in engineering or applied science, post graduate qualification preferred Minimum of

Description: Activities Executes manufacturing activities in the area of Drug Product according to ... Operating, setting up and cleaning production equipment and premises for the production of liquid and ... timely and with high quality the required production documentation (preparation, execution and review of ... process changes and CAPAs related to processes within required timelines Performs training activities of ... SOP execution Strong team orientation Effective communication skills and interaction with a variety of

In this role, the Cost Engineer will take charge of overseeing and coordinating all cost control activities ... reports for the project, which include, but are not limited to, budgets, commitments, Value of Work ... Fosters a culture of ‘cost awareness and communication’ within the team to ensure clarity and accuracy ... Project Duration: 12 Months Starting Date: ASAP Place of Work: Visp Responsibilities Prepares cost control ... communication and support as needed Analyzes data to understand variances from the plan and the impact of

Familiar with the financial and organizational complexities of CAPEX projects. ... including risk assessment, financial evaluation, analysis, and performance tracking across projects of ... Develop, implement, and maintain project reporting and cost tracking systems tailored to the needs of ... the project and finance teams to ensure accurate cost reporting, cash flow forecasting, and handling of

Deliver robust estimates and reports of EAC. ... Main Responsibilities: Understand various aspects of the project, including technical scope and content ... Proficient in English; Business German (B2) advantageous. 10+ years of experience as a Cost Manager in