Careers

Gsap is the largest consulting firm in Israel for providing first-rate professional services to pharmaceutical, medical devices, biotechnology, medical cannabis, and cell therapy companies.
Gsap has around 60 full-time employees.

Our employees are our ambassadors and they bring the company’s values to our customers which is what makes Gsap unique.

We are looking for enthusiastic, independent people who enjoy challenges and self learning.

We need people that share our vision: help companies by accelerating the development of safe and effective pharmaceutical and medical device products to patients world-wide.
The values that guide us lead us in creating real change in society and the medical industry.
If you have always dreamed of leading significant processes, taking part in interesting and complex projects and being part of a fast growing leading company,
Send Us Your Resume And We Will Be In Touch!

 

Gsap office
https://gsap.co.il/en/careers/apply/

  • Advanced Therapies

    • Advanced Therapies Quality and Regulatory Project Manager (1812)

      Gsap is expanding and is recruiting a project manager in the field of advanced therapies. to join our team of experts! If you have suitable experience and are interested in a full-time dynamic position in a ground-breaking field - apply and we will be in touch!

      Requirements:
      Relevant academic education: Biology / Biotechnology / Pharmacy
      Advanced degrees – a big advantage
      At least 5 years experience in QA. Advantage for a QA manager position or similar managerial position.
      Proven knowledge of quality management in GMP. Writing procedures, training employees, managing investigations, managing materials, certifying suppliers.
      Advantage will be given to experience in:
      Quality in aseptic production
      Laboratory quality
      high level English

  • Medical Devices

    • Quality and Regulatory Project Manager- Digital Health (1807)

      Gsap is growing and recruiting experts in Digital Health Regulation! If leading projects in a hot and developing field interests you and you are interested in diverse work in a flexible and unique work environment - send your resume and we will be in touch!

      : Requirements

      Bachelor’s degree in Software Engineering, or a related field.

      Proven experience in Digital Health for Medical Device products

      Profound understanding of IEC62304, ISO 13485, and other relevant standards and regulations, as well as the V&V tests

      Advantage: experience with submissions to FDA and/or Europe

      Capabilities to work with customers, self-learning

      manage projects and perform tasks with a high level of professionalism and responsiveness

      .

    • Regulation Experts in Medical Devices (1809)

      We are recruiting Regulation Experts for Medical Device! Do you have proven experience in Quality and Regulation of Medical Devices? Are you looking for a challenging, dynamic job in a great work environment? Submit your resume and we'll be in touch!

      Requirements:

      B.Sc. degree or higher in Biotechnology/ Electronics/ Biomedical/ chemistry / engineering Deep understanding in testing and validation of medical devices
      Deep understanding of relevant regulations and standards such as
      ISO 13485, ISO 14971, EU-MDR, 21CFR820, MDSAP
      English at high-level
      High self-learning ability and ability to deal with challenges
      Ability to work in a multi-tasking and changing environment

  • PHARMACEUTICALS

    • Pharma Regulation Project Manager (1811)

      Gsap is growing and recruiting project manager in the field of Pharma Regulation. Have 3-5 years of experience in the pharma / biotechnology / cell therapy industry? Interested in a diverse job in a work environment that is unparalleled? Submit your resume and we'll be in touch!

      Requirements:

      M.Sc. or Ph.D. degree in Life Sciences / Biology / Chemistry

      Knowledge and experience in working with regulatory authorities

      Proven experience in handling regulatory issues and problems

      Knowledge and experience working with FDA databases

      Knowledge and experience with chemical and biological drug development, with 505 (b)2 regulation and combinations

      Understanding preclinical and clinical requirement for preIND

      IND, NDA and/or other submissions

      English at mother tongue level

  • Gsap CRO

  • Engineering and Validation

Skip to content