תעסוקה

דרושים בפארק

CLEAN ROOMS ENGINEER דרוש/ה  לחברת אורג'נסיס בע"מ


The job is located in Bar Lev industrial park

GMP Translation manager
DUTIES & RESPONSIBILITIES
Planning, writing, execution, and monitoring of projects of setting-up GMP facilities globally and implementation of new therapies.
Planning, coordinating, writing, and following up of work plans for network centers
Performing gap analysis for potential network partners.
Writing gap analysis & risk analysis reports, presenting them, and submission to the management
Communicate with global teams and clients.
Working on projects in Israel and abroad
Continues communication with local partners, QA members (local & global), and operation teams (local & global).
REQUIREMENTS:
Proven background in large scale project management
English at a very high level – both written and oral - a Must (other languages - an advantage).
Experience in the pharmaceutical industry and clean rooms - a major advantage
Experience in GMP environment – a major advantage
Excellent personal & communication skills, highly motivated
Ability to adjust to quick changes
Open-minded and flexible thinking
Solution driven attitude
Organized, responsible with good self-management skills
Team player
Demonstrated knowledge of cleanrooms operating principles, practices, and procedures.
Experience using Excel, Word, and other office applications.
Ability to communicate effectively with a diverse clientele base.
Ability to work cooperatively with co-workers and the public.

Pls send your CVs to info-OBI@orgenesis.com




דרוש/ה GMP Readiness & Tech Transfer Integrator לחברת אורג'נסיס בע"מ


The job is located in Bar Lev industrial park GMP Readiness & Tech Transfer Integrator DUTIES & RESPONSIBILITIES Planning, writing, execution, and monitoring of projects relating to set-up of GMP facilities and implementation of new therapies. Planning, writing, and following up of work plans Performing gap analysis for potential cleanroom and/or facilities, and report writing Writing gap analysis & risk analysis reports Communicate with global teams and clients. Working on projects in Israel and abroad Continues communication with local partners, QA members (local & global), and operation teams. REQUIREMENTS: Proven background in large scale project management English at a very high level – both written and oral - a Must (other languages - an advantage). Experience in the pharmaceutical industry and clean rooms - a major advantage Experience in GMP environment – a major advantage Excellent personal & communication skills, highly motivated Ability to adjust to quick changes Open-minded and flexible thinking Solution driven attitude Organized, responsible with good self-management skills Team player Demonstrated knowledge of operating principles and practices, and procedures. Experience using Excel, Word, and other office application in high level Ability to communicate effectively with a diverse clientele base. Ability to work cooperatively with co-workers and the public. Pls send your CVs to info@at-vio.com




Quality Control Method Development Team Leaderדרוש/ה


Quality Control Method Development Team Leader The job is located in Bar-Lev industrial park The position is a full-time job and appeals to both men and women JOB Description Suggest, design, develop and implement biological QC assays for various projects according to relevant regulatory guidelines Building and guiding the team to develop R&D assays into QC tests Leading qualification and validation projects Perform data analysis, interpretation, and presenting the data for appropriate decision making Writing & reviewing protocols, reports, and formal working documents Work on multiple projects with multiple teams Hands-on lab work Managing a growing team with multiple disciplines JOB REQUIREMENTS Master’s in engineering or Ph.D. degree in Biology, Biochemistry and Biotechnology; and relevant experience in a similar position in the sector of biotech/pharma/cell therapy – mandatory Experience as a team leader Hands-on experience with cell-based bioassays, FACS, ELISA, and qPCR Experience with Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP) Experienced with cellular assay development including qualification and validation process Adaptability to changing work assignments and priorities Excellent teamwork Excellent interpersonal and communication skills Able to prioritize different activities Able to identify opportunities for continuous improvements and enable implementation Well organized, methodologic, quick learner, team player, motivated and responsible Assertive and working well under pressure Fluent English: oral and written, experience with scientific writing This position may include occasionally traveling abroad Pls send your CVs to info@at-vio.com




דרוש/ה TECHNICAL WRITER (outsourced) DUTIES & RESPONSIBILITIES


TECHNICAL WRITER (outsourced)

DUTIES & RESPONSIBILITIES

  1. Write and revise cell therapy manufacturing documents, including but not limited to Master Batch Records, Analytical Standard Operating Procedures (SOPs), Quality Control Sheets, Material Specifications
  2. Responsible to route documents for review through a document management system.
  3. Intense collaboration with development project leaders, quality assurance, and project managers.

REQUIREMENTS:

  • Associate's degree required. Education or experience in the biotech field and/or working with GMP documents is highly desirable.
  • Technical writing experience, preferred in cGMP setting.
  • Computer software skills including Microsoft Office, time management
  • Fluent in English writing
  • The work will be done remotely

Pls send your CVs to Info-OBI@orgenesis.com




Bioreactor Specialist דרוש/ה


The job is located in Bar Lev industrial park

Bioreactor specialist

JOB DESCRIPTION
Member of the development department.
Lead multi-disciplinary project team; serve as a team member on other projects.
Cell therapy bioreactors process development.
Writing and executing protocols for process development experiments.
Hands-on lab work.
Writing reports and preparing scientific and technical presentations.
Participating in technology transfer from/to the customer in Israel and abroad.
JOB REQUIREMENTS
Previous experience in bioreactor cell culturing for at least 2 years.
Previous experience in animal cell cultures
A relevant degree in biotechnology/biomedical engineering.
Strong technical skills
Excellent interpersonal skills.
Well organized, methodologic, quick learner, team player, motivated, and responsible.
Working well under pressure and dynamic environment
Fluent English: oral and written.
Preference will be given to candidates with previous GMP/GLP experience.

CV can be submitted at: info-OBI@orgenesis.com





CLEAN ROOMS ENGINEER דרוש/ה  לחברת אורג'נסיס בע"מ


The job is located in Bar Lev industrial park

GMP Translation manager
DUTIES & RESPONSIBILITIES
Planning, writing, execution, and monitoring of projects of setting-up GMP facilities globally and implementation of new therapies.
Planning, coordinating, writing, and following up of work plans for network centers
Performing gap analysis for potential network partners.
Writing gap analysis & risk analysis reports, presenting them, and submission to the management
Communicate with global teams and clients.
Working on projects in Israel and abroad
Continues communication with local partners, QA members (local & global), and operation teams (local & global).
REQUIREMENTS:
Proven background in large scale project management
English at a very high level – both written and oral - a Must (other languages - an advantage).
Experience in the pharmaceutical industry and clean rooms - a major advantage
Experience in GMP environment – a major advantage
Excellent personal & communication skills, highly motivated
Ability to adjust to quick changes
Open-minded and flexible thinking
Solution driven attitude
Organized, responsible with good self-management skills
Team player
Demonstrated knowledge of cleanrooms operating principles, practices, and procedures.
Experience using Excel, Word, and other office applications.
Ability to communicate effectively with a diverse clientele base.
Ability to work cooperatively with co-workers and the public.

Pls send your CVs to info-OBI@orgenesis.com




דרוש/ה GMP Readiness & Tech Transfer Integrator לחברת אורג'נסיס בע"מ


The job is located in Bar Lev industrial park GMP Readiness & Tech Transfer Integrator DUTIES & RESPONSIBILITIES Planning, writing, execution, and monitoring of projects relating to set-up of GMP facilities and implementation of new therapies. Planning, writing, and following up of work plans Performing gap analysis for potential cleanroom and/or facilities, and report writing Writing gap analysis & risk analysis reports Communicate with global teams and clients. Working on projects in Israel and abroad Continues communication with local partners, QA members (local & global), and operation teams. REQUIREMENTS: Proven background in large scale project management English at a very high level – both written and oral - a Must (other languages - an advantage). Experience in the pharmaceutical industry and clean rooms - a major advantage Experience in GMP environment – a major advantage Excellent personal & communication skills, highly motivated Ability to adjust to quick changes Open-minded and flexible thinking Solution driven attitude Organized, responsible with good self-management skills Team player Demonstrated knowledge of operating principles and practices, and procedures. Experience using Excel, Word, and other office application in high level Ability to communicate effectively with a diverse clientele base. Ability to work cooperatively with co-workers and the public. Pls send your CVs to info@at-vio.com




Quality Control Method Development Team Leaderדרוש/ה


Quality Control Method Development Team Leader The job is located in Bar-Lev industrial park The position is a full-time job and appeals to both men and women JOB Description Suggest, design, develop and implement biological QC assays for various projects according to relevant regulatory guidelines Building and guiding the team to develop R&D assays into QC tests Leading qualification and validation projects Perform data analysis, interpretation, and presenting the data for appropriate decision making Writing & reviewing protocols, reports, and formal working documents Work on multiple projects with multiple teams Hands-on lab work Managing a growing team with multiple disciplines JOB REQUIREMENTS Master’s in engineering or Ph.D. degree in Biology, Biochemistry and Biotechnology; and relevant experience in a similar position in the sector of biotech/pharma/cell therapy – mandatory Experience as a team leader Hands-on experience with cell-based bioassays, FACS, ELISA, and qPCR Experience with Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP) Experienced with cellular assay development including qualification and validation process Adaptability to changing work assignments and priorities Excellent teamwork Excellent interpersonal and communication skills Able to prioritize different activities Able to identify opportunities for continuous improvements and enable implementation Well organized, methodologic, quick learner, team player, motivated and responsible Assertive and working well under pressure Fluent English: oral and written, experience with scientific writing This position may include occasionally traveling abroad Pls send your CVs to info@at-vio.com




דרוש/ה TECHNICAL WRITER (outsourced) DUTIES & RESPONSIBILITIES


TECHNICAL WRITER (outsourced)

DUTIES & RESPONSIBILITIES

  1. Write and revise cell therapy manufacturing documents, including but not limited to Master Batch Records, Analytical Standard Operating Procedures (SOPs), Quality Control Sheets, Material Specifications
  2. Responsible to route documents for review through a document management system.
  3. Intense collaboration with development project leaders, quality assurance, and project managers.

REQUIREMENTS:

  • Associate's degree required. Education or experience in the biotech field and/or working with GMP documents is highly desirable.
  • Technical writing experience, preferred in cGMP setting.
  • Computer software skills including Microsoft Office, time management
  • Fluent in English writing
  • The work will be done remotely

Pls send your CVs to Info-OBI@orgenesis.com




Bioreactor Specialist דרוש/ה


The job is located in Bar Lev industrial park

Bioreactor specialist

JOB DESCRIPTION
Member of the development department.
Lead multi-disciplinary project team; serve as a team member on other projects.
Cell therapy bioreactors process development.
Writing and executing protocols for process development experiments.
Hands-on lab work.
Writing reports and preparing scientific and technical presentations.
Participating in technology transfer from/to the customer in Israel and abroad.
JOB REQUIREMENTS
Previous experience in bioreactor cell culturing for at least 2 years.
Previous experience in animal cell cultures
A relevant degree in biotechnology/biomedical engineering.
Strong technical skills
Excellent interpersonal skills.
Well organized, methodologic, quick learner, team player, motivated, and responsible.
Working well under pressure and dynamic environment
Fluent English: oral and written.
Preference will be given to candidates with previous GMP/GLP experience.

CV can be submitted at: info-OBI@orgenesis.com





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