Key Responsibilities Develop and execute commissioning, qualification, and validation (CQV) protocols for DeltaV automation systems. Ensure that all DeltaV systems are validated according to industry standards and regulatory requirements, including GMP and FDA regulations. Collaborate with cross-functional teams to define automation and validation requirements and develop detailed validation pl...
Read moreI am representing a huge player within the Pharmaceutical Industry who are looking for someone to join their CSV team, supporting the team for 10 months. Your tasks are: Advice and support in the validation of computer-aided systems including checking and approval of documentation, maintaining / managing the overview list of computer-aided systems Support for […]
Read moreSummary: The focus of this task is on the release/certification of clinical investigational medicinal products. In addition to in-house training, you will be involved in specific customer projects. These projects are carried out both independently and together with our customers. Accompanying or carrying out audits is another part of your job. Our common goal is […]
Read moreMy client is looking for an energic consultant with a technical scientific background and initial (at least 2 years) experience in GMP/ GDP area (Packaging Labelling, Quality Operations and or Quality System) for a contracted role till end of the year. Daily Responsibilities: Reviewing the Batch Record of the CMO with the intent to ensure […]
Read moreMy client, a global technology and service provider, are looking for for a Supply & Demand Planner to join their team in St Gallen, Switzerland. As a Supply & Demand Planner within the Global Service Operation Team, your primary responsibility is to maintain equilibrium between customer needs and product inventories. Your daily tasks involve managing […]
Read moreGlobal Manager, Training Quality Lead In this role, you will drive the overall management of Procedural Document Management and Training Management activities throughout a leading Biopharma located in Switzerland. You will build a collaborative working relationship & partner with the business partners and cross-functional Quality Peers. Your responsibilities will be but not limited to: DOCU...
Read moreGlobal Manager, Training Quality Lead In this role, you will drive the overall management of Procedural Document Management and Training Management activities throughout a leading Biopharma located in Switzerland. You will build a collaborative working relationship & partner with the business partners and cross-functional Quality Peers. Your responsibilities will be but not limited to: DOCU...
Read moreDevelopment Engineer Position brief: To help strengthen technical core competencies of the R&D team and develop new technologies (Dental products) Responsibilities include: Plan, undertake, and record technical exploratory projects (pre-development), as well as workstreams to strengthen existing technical competencies. Contribute to development projects with technical expertise and investig...
Read moreSystems Engineer (Senior) CDMO, focused on the In Vitro Diagnostics and Life Science industries. Responsibilities Technical leadership of development projects for optoelectronic modules. Directly interacting with customers to elicit, formulate, and negotiate product requirements. Determine design specifications, together with the specialists in your development team. Offer support to the Sales ...
Read moreCompany – Scienta are teaming up with an outstanding BioPharma focusing on the research into Oncology & Infectious diseases (Drug development, manufacturing…etc). Based within the heart of Switzerland this role offers and outstanding opportunity for someone looking to relocate/take on a new challenge. Our client is now looking for a Quality Team Lead to oversee […]
Read moreThis position is based in Lausanne, Switzerland, and is able to support relocation of EU candidates. The Company We are working with an independent biopharma company that is focused on the clinical development of high potential candidates in the Oncology and Infectious Disease space, with the hopes of bridging the gap between discovery products and […]
Read moreCompany – Scienta are teaming up with an outstanding BioPharma focusing on the research into Oncology & Infectious diseases (Drug development, manufacturing…etc). Based within the heart of Switzerland this role offers and outstanding opportunity for someone looking to relocate/take on a new challenge. Our client is now looking for a Quality Team Lead to oversee […]
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