PCR Superstar / Molecular Assay Developer

Medizinische Berufe, Pädagogik, Betreuung & Pflege

Datum und Uhrzeit
Start:

Ab Sofort

Stunden pro Woche:

38.5

Lohnangabe

Nach Vereinbarung

Vorstellungstermin

Vorstellungstermin nach Vereinbarung

Dienstverhältnis

Unbefristet

Job-Beschreibung und Hinweise für PCR Superstar / Molecular Assay Developer

INTRODUCTION:

For our client, a medical technology manufacturer located in the area of Zurich, we are looking for an individual as

PCR Superstar / Molecular Assay Developer

(Permanent employment, fulltime). The earliest start date is as soon as possible.


ASSIGNMENT DESCRIPTION:
  • Own and lead all aspects of molecular assay development with a focus on multiplex, real-time PCR and isothermal amplification
  • Perform verification and validation of the companys breath collector in combination with molecular IVD assays using contrived and clinical samples
  • Support the development, improvement, and evaluation of the breath collection IVD device
  • Optimize DNA/RNA lysis and extraction
  • Execute assay and reagent troubleshooting, optimization, and validation experiments
  • Be the clients go-to person if it comes to molecular assays and IVD's, share your knowledge and train other team members in the lab
  • Manage R&D projects including with external partners and ensure project deliverables and timelines are met
  • Develop, update, and implement SOPs
  • Ability to multitask and switch projects as priorities change
  • Manage, analyze, and communicate results to your team and stakeholders within the organization
  • Help building our quality management system
  • Assume different roles and grow into new technical areas and/or leadership role as needed


REQUIRED PROFILE:
  • PhD, MSc or BSc in Molecular Biology, Life Sciences, or related degree
  • In-depth knowledge of PCR, multiplex PCR, real-time PCR, DNA and RNA isolation, assay design and optimization
  • 3+ years of relevant experience developing molecular assays (PCR and or other NAATs)
  • 2+ years of relevant experience with in-vitro diagnostic products development within ISO13485 environment
  • Experience with the development and manufacturing of clinical sampling or lab consumables or test cartridges is a strong plus
  • Experience with CLSI guidelines and IVD verification and validation is a strong plus
  • IVD project management experience is a strong plus
  • Experience with respiratory infectious disease diagnostics is a strong plus
  • Demonstrated ability to work effectively across multiple disciplines such as biology, engineering, and manufacturing is desirable
  • Highly proactive and self-directed with strong scientific integrity and willingness to always question results, including your own
  • Hands-on team player with strong “can do”, analysis and problem-solving skills who likes to tackle challenges, improve own skills, and help shape the company's future
  • Proficient written and oral communication skills in English, fluency in German is a plus
  • Applicants must be either Swiss citizens, EU nationals or have the legal right to live and work in Switzerland


Application process:

Interested? You can find more information here: Infopackage. Please apply via the "Bewerben" button below and answer all questions, otherwise we will be unable to process your application.

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