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://www.gsap.co.il/careers/apply/
  • Medical Devices

    • Specialist in V&V testing of Medical Device products

      Gsap is growing and recruiting an expert for V&V tests of products in Medical Devices! If you have experience with V&V tests of a product in Medical Device and are interested in diverse work in a unique work environment - send your resume and we will be in touch!

      Requirements:

      B.S. degree or higher/ Practical Engineer
      At least 3 years of experience in Medical Device
      Familiarity with ISO 13485, Design controls, Risk management according to ISO 14971
      Proven experience with V&V testing of a product in Medical Devices including familiarity with relevant standards and knowledge to communicate with laboratories:
      EMC & Electrical Safety, Biocompatibility and Chemical Characterization,Re-processing Validation – Cleaning and Sterilization / Disinfection Sterilization, Validation (Gamma & ETO, Bioburden, Ster) Packaging, Integrity and Shelf life (Transportation, package testing requirements and microbial barrier)
      English at high-level
      High self-learning ability

    • Quality and Regulatory Project Manager- Digital Health

      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:

      B.Sc. degree or higher in Software / Electronics / Biomedical
      At least 2 years of experience in the field
      Leading Software Regulation Projects- IEC62304, 14971ISO, Submissions(Software Chapter)FDA, CE
      GDPR, HIPPA, Cyber ​​Security Lead
      Ability to work with software developers
      English at high-level
      High self-learning ability and ability to deal with challenges
      Significant work with clients

    • Quality Engineer for Design and Development of Medical Device

      Gsap is growing and recruiting a Quality Engineer for design and development of Medical Device! If you have experience in Quality Engineering in Medical Device and are interested in diverse work in a flexible and unique work environment - send your resume and we will be in touch!

      Requirements:

      B.Sc. degree or higher/ Practical Engineer
      At least 2 years of experience in Quality Engineering in Medical Device
      in design and development control (Design controls), including risk management according to ISO 14971
      English at high-level
      Ability to work in a multi-tasking and changing environment
      High self-learning ability

    • Project Manager in Quality and Regulation of Medical Devices

      We are recruiting Project Manager 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
      Proven experience in Quality and Regulation Of Class II and above in Medical Device- must
      Certificate of Certified Quality Engineer ICQE \ CQE- Advantage
      English at high-level
      Ability to work in a multi-tasking and changing environment
      High self-learning ability

    • Regulation Experts in Medical Devices

      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

    • Quality and Regulation Engineer in Medical Device

      We Are Looking For a Quality and Regulation Engineer who enjoys challenges and self learning. If you are interested, submit your resume and we'll be in touch!

      Requirements:

      Relevant education: Engineer / Practical Engineer / Science

      At least one year of experience in Quality Engineering in Medical Device

      Familiarity with ISO 13485 and regulatory requirements in US and Europe such as MDR and 21CFR820

      High level of English

      High self-learning ability and ability to deal with challenges

      Ability to work in a multi-tasking and changing environment

  • PHARMACEUTICALS

    • Pharma Quality Project Manager

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

      Requirements:

      At least 3-5 years of experience in Quality Management in pharma / biotechnology / cell therapy industry
      Experience in a Sterile / Aseptic ward
      high-level of English
      High self-learning ability and ability to deal with challenges
      Ability to work in a multi-tasking and changing environment

    • Pharma Regulation Project Manager

      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

  • Clinical

    • Clinical Research Associate- CRA

      We are a CRO boutique that provides end-to-end clinic services, from the planning stage to the research summary stages in a variety of areas. If you are motivated and interested in learning, deepening and gaining real experience at all stages of clinical research, we are the address.

      Requirements

      Academic in the field of Natural science / health - preference for advanced degrees
      Scientific approach, scholarship, thoroughness and ability to draw conclusions from information
      Ability to work in a changing and multi-tasking environment
      Experience in scientific writing, editing scientific documents, protocols and preparing research plans
      Practical experience of 2-3 years in monitoring research in the Pharma / Medical Device industry / CRO
      Experience in locating and selecting centers, contracts, training, opening and closing centers
      Experience in managing research files, submissions, and reporting to authorities
      Training and motivation skills for the operation of medical staff and service providers
      High level of English
    • Clinical Quality Assurance Specialist

      We are looking for a quick learner person, adaptive, with high service orientation and problem-solving attitude to join our clinical team. The Clinical Quality Assurance Specialist will be responsible for QMS, SOPs writing & maintenance, Internal and external audits and more.

      Requirements:

      • Deep knowledge and understanding of ICH-GCP
      • Significant experience in Clinical Trials Execution and ICH-GCP quality aspects
      • Ability to perform audits, preparation of Plans, CAPAs and reports

    • Clinical Trial Manager-CTM

      We are a CRO boutique that provides end-to-end clinic services, from the planning stage to the research summary stages in a variety of areas. If you are motivated and interested in learning, deepening and gaining real experience at all stages of clinical research, we are the address.

      Requirements:
      Degree in Natural Sciences / Medicine / Biomedical Engineering

      Significant experience in leading clinical trials and research management

      Deep knowledge of accepted standards and procedures in clinical trials

      Scientific and design capabilities, operations research, information analysis and conclusions

      Abilities for drafting, writing, editing and examining clinical content

      Ability to deal with service providers and lead processes

      Ability to adapt to a changing and complex work environment

      Ability to learn and conduct oneself independently

      Excellent  English

  • Engineering and Validation

    • Validation Project Manager- Pharma industry

      Gsap is growing and recruiting project manager in the field of Validation and Engineering in the Pharma industry Have a relevant experience? Interested in a diverse job in a work environment that is unparalleled? Submit your resume and we'll be in touch!

      Requirements:
      Proven validation experience in the pharmaceutical industry in the field of systems, equipment, software and process.
      Experience in managing and leading projects
      High level English
      High self-learning ability and ability to deal with challenges
      Ability to work in a multi-tasking and changing environment

    • Quality Operations / Process Engineer in Medical Device for Project Management Position

      Gsap is growing and recruiting project manager in the field of Validation and Engineering in the Medical Devices industry Have a relevant experience? Interested in a diverse job in a work environment that is unparalleled? Submit your resume and we'll be in touch!

      Requirements:
      Proven experience in quality engineering in the medical device industry
      Good familiarity with production processes, process controls, risk management.
      Experience in managing and leading projects.
      Experience in validation for production lines, Process Validation, TMV
      high-level English
      Ability to self-learn and face challenges
      Ability to work in a multi-tasking and changing environment

  • Advanced Therapies

    • Advanced Therapies Quality and Regulatory Project Manager

      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