At-Vio Careers

Process Development Engineer

Position No. 20

Job description
  • Cell therapy process development and culturing methods • seed train and downstream design • Writing equipment SOPs, working protocols and experiments reports • Gap analysis performance • Taking part in technology transfer form/to the customer • Training of new personnel in Israel and abroad.
Job requirements
  • Previous experience in Bioreactor cell culturing- mandatory!
  • Previous experience in animal cell cultures- mandatory!
  • Previous experience in downstream processes and viruses in particular- advantage
  • 5 years experience or MSc and above in Biology/ Biotechnology/ other relevant fields
  • High level in English • Well organized, Methodologic, quick learner, team player, motivated and responsible
Preference will be given to candidates with previous GMP/GLP experience
        CV can be submitted at: info@at-vio.com

        Project Manager

        Position No. 22

        Job description

        1. Working closely with clients from Israel and abroad
        2. Leading development projects
        3. Constructing working plans
        4. Project budget and schedule monitoring
        5. Writing reports
        6. Constant work and communication with the development team.

        The job includes flights to different countries.

        Job requirements

        • Previous experience in animal cell cultures- mandatory!
        • MSc with at least 7 year's experience in the cell therapy industry or PhD in Biology/ Biotechnology/ other relevant fields with minimum 3 years of biotech / pharma industrial experience.
        • High level in English
        • Well organized, Methodologic, quick learner, team player, motivated and responsible
        • Assertive, good communicator, good in working under pressure.

        Preference will be given to candidates with previous GMP/GLP experience or working with viruses.

        CV can be submitted at: info@at-vio.com

        System Engineer

        Position No. 23

        Job description
        1. Writing system definition including URS or PRD from basic concept to prototype.
        2. Contribute Systems Engineering expertise. Work with multidisciplinary teams to explore, de-risk, and create product requirements and effective product architectures.
        3. Establish risk management activity to drive mitigation of risks through product design.
        4. Oversee design output documentation. Create, update, and maintain the Design History File and ensure adherence to best practices and regulatory requirements.
        5. Transfer designs to manufacturing. Maintain the Design Master Record and execute design transfer activity in conjunction with a cross-functional team.
        6. Liaise with vendors and subcontractors for problem resolution.
        Job requirements
        • BSc degree in Mechanical or Electronical Engineering or a related subject.
        • Minimum industrial experience of 3 years in designing medical device.
        • Knowledge in solid works or equivalent graphical software.
        • Familiarity with analog, digital, and RF electronics.
        • Advantage: demonstrating applied expertise in FDA requirements (21 CFR 820) and medical device regulations.
        • Fluent in spoken and written English; Speaking additional languages is an advantage.
        • Well organized, quick learner, team player, motivated and responsible.
        • Working well under pressure.
        CV can be submitted at: info@at-vio.com