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Work as a software developer without experience - for graduate students |
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Category: |
Biotechnology, Engineering, Chemistry, Life Sciences, Pharmacy/Pharmacology, Healthcare, IT/Hardware/Software
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Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
No experiece |
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Area(s) of expertise desired: |
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Description: |
InfinityLabs R&D(a Matrix company) is looking for Graduates with high grades who want to develop a career! You have the option to change your future by 180 degrees. If you have high analytical capabilities and you are interested to work in the high-tech industry - this is your chance to try your luck and test your suitability for work as a software developer. Qualifying will be given training at the expense of the company.
Full-time job.
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Requirements: |
Bachelor's degree average of 85 and above.
Independent learning ability.
high-level English.
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Director, Clinical Operations |
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Category: |
Life Sciences, Clinical Research, Pharmacy/Pharmacology
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Education: |
Bachelors |
Position type: |
Full Time |
Experience: |
10+ years |
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Area(s) of expertise desired: |
Clinical Research, Regulatory Affairs, Start-Up
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Description: |
The Role:
Reporting to the Senior Director, Clinical Operations & Site Head, the Director of Clinical Operations will be responsible for leading and managing the execution of Eloxx’s clinical studies from protocol inception through study closure. This key role will manage, plan and execute clinical studies, including creating and managing study timelines, budgets and study management plans in a full out-sourced model to ensure that our corporate goals. This is a great opportunity for visibility and professional growth; the Director of Clinical Operations will manage a team of Clinical Project Managers and partner with the Senior Director to represent the Clinical Operations team cross-functionally and with key stakeholders.
Responsibilities:
• Ensures that clinical trial projects are properly resourced, managed and executed within budget and in accordance with established timelines and quality standards.
• Oversees the day-to-day clinical operations through a team of Project Managers with a focus on vendor management(e.g., CRO, laboratories), monitoring clinical trial recruitment rate, and coordination of activities.
• Executes high quality, integrated cross-functional plans for the project/clinical trial.
• Represent Clinical Operations in cross-functional teams, clinical meetings and regulatory meetings. Provide regular status updates to senior management.
• Provide strategic input and drive the planning and execution for assigned clinical trials with direct responsibility for time, cost, quality, and risk mitigation.
• Responsible for the oversight of protocols development; protocol preparation, amendments, CRF, informed consent form, operations and other documentation required for conduct of a clinical trial.
• Accountable for internal clinical trial files and documents.
• Participates and manages investigator meetings and follow up.
• Travels for meetings and site visits when necessary.
• Maintains proper communications with other departments to ensure good relationships in connection with ongoing set up and progress throughout trial planning and execution.
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Requirements: |
Competencies Include:
• Complex problem-solving abilities with a focus on accomplishing assigned goals and objectives in a dynamic environment.
• A team player who is able to effectively and flexibly lead cross functional teams across diverse cultures, backgrounds and styles.
• Excellent communications and presentation skills, able to effectively inform key stakeholders and management of the status, issues and solutions.
• Strong organizational and planning skills are required, with a proven ability to manage budgets and timelines.
• Detail-oriented, a self-starter and comfortable with broad responsibilities in a fast-paced, small company environment.
• Excellent computer skills, proficiency with project management software tools.
• Prepared to travel internationally (US and EU) for approximately 7-10 days once every 2-3 months.
• Flexibility to work US hours a few times a week.
Experience:
• Minimum of 10 years’ experience in the pharmaceutical industry, with 5-7 years’ direct experience in planning and managing global clinical trials.
• Strong people management skills with experience managing at least 2 or 3 direct reports required.
• Strong bi-lingual verbal and writing skills in English and Hebrew required.
• Extensive experience managing clinical programs, CROs, budgets and timelines.
• Regulatory/EMA/FDA experience.
• Good working knowledge of medical terminology, physiology and pharmacology and an excellent knowledge of applicable U.S. and international regulations and guidelines.
• Solid understanding of pharmaceutical clinical development processes and have experience with clinical monitoring.
• Ability to thrive in a fast-paced, entrepreneurial environment with busy, high performing colleagues.
• Strong leadership skills and self-awareness.
• Experience presenting to a varied audience, including investors and upper management.
Education:
• Bachelor’s Degree or equivalent biologic science degree is preferred.
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JB-169 Computational Chemist |
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Category: |
Biotechnology, Chemistry, Pharmacy/Pharmacology
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Education: |
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Position type: |
Full Time |
Experience: |
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Area(s) of expertise desired: |
Academic, Applied Chemistry, Biochemistry, Bioinformatics, Cheminformatics, Chemistry, Computational Chemistry
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Description: |
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Requirements: |
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RA Project Manager |
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Category: |
Biotechnology, Pharmacy/Pharmacology, Regulatory Affairs
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Education: |
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Position type: |
Full Time Employee |
Experience: |
2 years |
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Area(s) of expertise desired: |
Biology, GMP, Regulatory Affairs
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Description: |
Omrix, a J&J Bio-Pharmaceutical company, is seeking RA Project Manager for its’ Nes-Ziona or Jerusalem Site. The position includes Providing Regulatory Affairs support, Generating and managing submission documents for new products or changes to existing files;
Assessing company activities, including new efforts and modifications for existing products, for regulatory impact and creating and executing regulatory strategies for implementation; Tracking requirements of regulatory agencies and implementing file updates accordingly.
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Requirements: |
Qualifications:
Degree in biology, chemistry, or another related field.
At least 2 years of Similar industry experience (QA / Medical Device) -
Experience in biologics Regulatory Affairs an advantage.
Familiarity with regulatory requirements
Working experience with regulatory authorities
Excellent communication, interpersonal and organization skills.
Computer skills: Microsoft Office applications.
Language: mother-tongue level English required
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Job Offer in UK |
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Category: |
Engineering, Chemistry, Clerical/Administrative, Pharmacy/Pharmacology
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Education: |
Masters |
Position type: |
Part Time |
Experience: |
3 years |
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Area(s) of expertise desired: |
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Description: |
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Engineers, Foremen, Captain, Mate Engineer, 2nd Engineer, 2nd/3rd Officer, Deckhand, Steward, Chef, Seafarers , Crew Job Seekers , Chief Engineer , Doctors, Nurses, Laborers, Pharmacists, Dentists, Masons, Plumbers, Drivers, Heavy equipment operators, architects, Surveyors, Customer Care Representatives.
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Requirements: |
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CLEAN ROOM CELL PROCESSING SPECIALIST |
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Category: |
Biotechnology, Pharmacy/Pharmacology
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Education: |
Bachelors |
Position type: |
Full Time Employee |
Experience: |
2 years |
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Area(s) of expertise desired: |
Academic, Biology, Cell Biology, GMP, Immunology, Microbiology, Molecular Biology, Start-Up
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Description: |
Company:
Immunovative Therapies, Ltd. is a biopharmaceutical start-up company headquartered in Jerusalem and Specializing in the development and production of immunotherapy drug products incorporating living Immune cells as the active ingredients.
• Description:
• Process patient blood and serum samples.
• Work with human PBMC and maintain mammalian cell cultures.
• Perform routine cell staining and flow cytometry on clinical samples.
• Perform immunological-based techniques including ELISA, cytokine bead array and functional T cell assays (e.g., ELISPOT and cell proliferation).
• Coordinate with team members to complete routine laboratory tasks such as reagent/supplies liquoting, restocking and ordering.
• Maintain laboratory equipment and notebooks, computer files/databases.
• Follow established standard laboratory operating procedures.
• Hands-on lab work with long hours in a clean room environment
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Requirements: |
Requirements:
• Impeccable aseptic technique skills
• Ability to follow written instructions.
• Knowledge of GMP manufacturing and prior experience working in a clean room.
• Primary responsibility will be in cell production department.
• BSc. in the biological sciences with 2+ years of related professional laboratory experience with extensive background in aseptic technique.
• Experience with flow cytometry is an advantage
• Experience of handling human samples and cell cultures
• Highly organized, detail orientated and have strong analytical and problem solving skills
• Strong record-keeping skills
• Adaptable and multi-tasking
• Must work well in a team environment with admirable interpersonal and communication skills in both English and Hebrew (written and oral)
Working Conditions & Physical Requirements:
• This job is performed primarily in a class 10,000 clean room environment with full gowning and , working with human blood/cells in a BSC
• Will require work with hazardous materials (human blood and blood components)
• Requires occasional evenings and weekends work
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Extra Money in a new Sales Project |
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Category: |
Biotechnology, Chemistry, Life Sciences, Pharmacy/Pharmacology, Healthcare, Sales/Marketing
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Education: |
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Position type: |
Full Time Employee |
Experience: |
No experiece |
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Area(s) of expertise desired: |
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Description: |
International nutrition company is looking for 5 new employees to join a dynamic sales team.
Challenging job in marketing & sales.
Min 10 hrs/week.
Extra 2000-4000 nis (predictable income)
Option to work from home.
Please send CV to: project@slimail.com
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Requirements: |
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Please send CV to: project@slimail.com
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CRA |
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Category: |
Life Sciences, Clinical Research, Pharmacy/Pharmacology, Medical Equipment
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Education: |
Masters |
Position type: |
Full Time Employee |
Experience: |
2 years |
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Area(s) of expertise desired: |
Clinical Research
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Description: |
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Requirements: |
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Medical Director (9594) |
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Category: |
Management/Executive, Medical Management, Pharmacy/Pharmacology
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Education: |
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Position type: |
Full Time Executive |
Experience: |
5 years |
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Area(s) of expertise desired: |
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Description: |
Responsibility for global medical affairs of marketed innovative product:
work with investigators, clinical associates, marketing and legal to ensure timely execution of phase IV clinical studies.
Development of global Key Opinion Leader relations.
Lead and/or support meeting and congresses, including medical congress symposia, expert meetings, advisory boards and internal meetings.
Preparation and/or review of Medical and Marketing materials.
Responses to medical questions from market.
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Requirements: |
Requirements:
MD with 5-10 years of experience which includes experience in the pharmaceutical or Biotechnology Company.
Experience in a Global environment and/ or a previous similar role - a big advantage
Experience in leading clinical trials
MBA or business background - an advantage
Mother tongue level English
Excellent communication and presentation skills
Excellent analytical skills
Ability to work well in a global, complex, multi-interface structure
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Director, Manufacturing |
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Category: |
QA - Quality Control, Biotechnology, Engineering, Chemistry, Life Sciences, Clinical Research, Clerical/Administrative, Management/Executive, Medical Management, Pharmacy/Pharmacology, Medical Equipment, Regulatory Affairs, Healthcare, Sales/Marketing
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Education: |
Bachelors |
Position type: |
Full Time Manager |
Experience: |
10+ years |
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Area(s) of expertise desired: |
Bioanalytical Services, Biology, Manufacturing/Production
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Description: |
Summary
This position is responsible for the technical oversight of biomanufacturing activities at contract manufacturing organizations associated with the production of critical raw materials, Drug Substance and Drug Product.
Responsibilities
• Execute on time and cost the Manufacturing Supply Forecasts through oversight of third party manufacturers based in Japan, Israel and the US : Act as Person in Plant during manufacturing campaigns
• Conduct technical audits of manufacturing operations to identify opportunities for Continuous Improvement at third party manufacturers
• Technical review of batch documents
• Trouble shoot manufacturing issues and support QA in Deviation and CAPA activities
• Support QA in the technical review of Change Requests
• Assist the Chief Technology Officer in the development of budgets
• Provide data to populate the KPI program for Manufacturing
• Other projects and assignments as required.
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Requirements: |
Requirements
• BS Degree, in either bioengineering or a biological science.
• Fifteen-plus years experience in manufacturing of biological products
• Five-plus years in the management of biopharmaceutical manufacturing operations.
• Excellent communication skills in Hebrew, both oral and written.
• Profound knowledge of GMP requirements associated in biomanufacturing in the US and Internationally.
• Knowledge of the engineering aspects of biopharmacecutical manufacturing plants
• Experience working with CMO's
• Goal oriented with a problem solving mindset
• Proficiency with computers and major software packages, e.g. Microsoft Excel, Outlook, Powerpoint, Project
• Excellent communication skills in English, both oral and written.
• Travel - 25%
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