Clinical reviewer Visp VS Jobs

54 offene Stellen

QA for QC Data Reviewer

 ...das ist die Art von Arbeit, an der wir Teil haben möchten.  Zur Verstärkung unseres Teams suchen wir am Standort Visp eine/n QA Reviewer/in für QC. Ihre Aufgaben: ~Überprüfung der QC-Rohdaten ~Verantwortung für die Analyseergebnisse einschließlich der entsprechenden... 
Visp VS
vor 2 Monaten

Batch Record Review

Randstad Inhouse Services sucht im Auftrag der Lonza AG für eine temporäre Anstellung eine/n Mitarbeiter/in Batch Record Review. Die Anstellung ist per sofort voraussichtlich bis 31.08.2021 am Standort in Visp. Lonza ist heute ein weltweit führendes Unternehmen im Bereich... 
Visp VS
vor 2 Monaten

Batch Record Reviewer Betrieb (m/w/d)

 ...gross und klein, verbessern die Welt. Und das ist die Art von Arbeit, an der wir Teil haben möchten. Als betrieblicher Batch Record Reviewer sind sie zuständig für die selbstständige und zeitgerechte Durchführung der Herstellungsdokumentekontrolle nach betriebsinterner... 
Visp VS
Vor einem Monat

Junior QA Manager Batch Record Review

 ...improve the world. And that’s the kind of work we want to be part of. In Visp we are looking for a Junior QA Manager Batch Record Review IBEX™ to extend our team. You will report to the QA Operations Group Leader IBEX™, work in close collaboration with different... 
Visp VS
vor 2 Monaten

MSAT BioConjugates Process Expert

 ...track record in the manufacturing of BioConjugates from early clinical to large scale commercial supplies. Our dedicated Protein Conjugation...  ...management Process validation activities Annual product review (APQR) Representing the facility during process specific... 
Visp VS
Vor 1 Tag

Bioprocess Engineer in Cell banking

 ...from cell culture to filling including viability studies for clinical and commercial manufacturing projects as well as end of and post...  ...cell banksAdditional tasks include evaluating test results, reviewing production documentation, working on deviations, change requests... 
Visp VS
Vor 11 Tagen

QA Project Manager Ibex™

 ...the manufacturing processes of biopharmaceutical products for clinical and commercial supply. This includes oversight of QC/logistic/supply...  ...projects in internal and external meetings ~Responsible for review and final release of records such as  Standard Operating... 
Visp VS
Vor 25 Tagen

Head of MSAT BioConjugates Visp

 ...science and technology (MSAT) team to support the portfolio of clinical and commercial products in our facilities. The newly established...  .../extractable and compatibility assessments, annual product review, APQR) Responsible for the introduction of new technologies,... 
Visp VS
Vor 22 Tagen

QA Manager Drug Product Ibex

 ...responsibilities: Involvement in all quality related activities for the manufacturing processes of (Drug Product) for clinical and commercial supply Responsible for review and approval of manufacturing documents and records such as Standard Operating Procedures (SOP), Master... 
Visp VS
Vor 22 Tagen

Manager, Regulatory Affairs

 ...we want to be part of. In this exciting role, you will support clinical trial and product license applications for various CMC (...  ...Provide regulatory support for projects and project teams ~Write/review CMC sections for regulatory documents ~Prepare briefing documents... 
Visp VS
vor 2 Monaten

Head QC Biologics Projects

 ...department (knowledge, skills, resources). Manages and coaches Managers with supervised staff, including definition of targets, review and management of staff performance as well as definition of standards for people management executed by direct reports.... 
Visp VS
Vor 3 Tagen

Senior Bioprocess Engineer (m/f/d)

 ...preparation, inoculum seed train, waves, single-use bioreactors, large-scale stainless steel bioreactors and/or depth filtration for clinical and/or commercial mammalian manufacturing ~In downstream processing, you will be in charge of the purification of monoclonal... 
Visp VS
Vor 13 Tagen

Postdoc Quality Project Manager

 ...are meeting technical, quality, and supply chain requirements and to ensure the delivery of robust materials that are suitable for clinical and commercial manufacturing. Responsible for the Compliance and Quality of the Single Use Technology program. Participate... 
Visp VS
Vor 11 Tagen

QA Manager

 ...customers and internal teams such as MSAT (Manufacturing Science & Technology), Manufacturing, Engineering and Quality Control Review and approve Discrepancy Records and Change Requests, manage the process for notifying the customer about discrepancies / change requests... 
Visp VS
Vor 1 Tag

Senior Manager QA Strategic Growth CAPEX Project Initiation

 ...procedures and specifications. Be a member of the Projects Leadership team until basic design completion and CAR approval. Review and approve project and compliance documents and records Ensure that decisions are fully supported by global and local Quality... 
Visp VS
Vor 1 Tag

Senior Recruiter

 ...and negotiates to final acceptance of the offer.executes sourcing methodologies to effectively develop target candidate pipelines.reviews CV's/resumes, screen, and interview candidates. determines the fit while influencing and persuading candidates on employment... 
Visp VS
Vor 2 Tagen

Operational Excellence Manager

 ...excellence roadmap, assessing progress and defining actions Work with functional leaders to establish continuous improvement goals Review, report & improve metrics at appropriate levels of the business Align and prioritize innovation initiatives, and projects,... 
Visp VS
Vor 1 Tag

Bioprocess Engineer

 ...manufacturing equipment and making recommendations for resolution. ~Responsible for perform/support qualification activities ~Authoring and reviewing GMP-relevant documents and SOPs due to automation ~Supports regarding to automation questions during customer audits and visits... 
Visp VS
Vor 15 Tagen

Bioprocess Engineer (m/f/d)

 ...downstream processing (DSP) you will be in charge of the purification of monoclonal antibodies and other therapeutic proteins for clinical and commercial manufacturing projects Key requirements: Master’s Degree in Biotechnology, Biochemistry or related Life Science... 
Visp VS
vor 2 Monaten

Chemist QC / Chemiker(in) QC

 ...activities within the applicable discipline as well building up and sharing of knowledge within the QC department ~Creation, revision and review of cGMP documentation (SOP’s, Quality Instructions, protocols, reports…) based on a standard format related to quality control... 
Visp VS
Vor 4 Tagen