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Job Search Results: Jobs 1 - 10 of 183  View Titles Only  Page 1 of 19
 
Title   Company Name     Location   Date  
Job Offer in UK 

  LSC & Construction Engineer Ltd    All   28/6/2013 
Category: Engineering, Chemistry, Clerical/Administrative, Pharmacy/Pharmacology  
Education: Masters   Position type: Part Time  Experience: 3 years 
Area(s) of expertise desired:  
Description:
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.  
Requirements:
Certificates required  
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Clinical Research Associate/Senior Clinical research associate- office/home based 

  Hays Pharma    All, Izrael (anywhere)   6/11/2007 
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, IT/Hardware/Software  
Education:   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Clinical Research  
Description:
JOB FUNCTIONS/RESPONSIBILITIES:

Recruitment of investigators.
Co-ordinate all the necessary activities required to set up and monitor a study, including the following:
Identify investigators
Help, when requested, in preparation of regulatory submissions
Design patient information sheets and consent forms.
Ensure timely submission of protocol/consent documents for ethics/IRB approval.
Placement and initiation visits.
Conduct regular monitoring visits in accordance with site monitoring SOP / Sponsor site monitoring SOP, as appropriate
Maintain all files and documentation pertaining to studies.
Motivate investigators in order to achieve recruitment targets.
Complete accurate study status reports.
Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs.
Keep the project manager informed.
Process case record forms to the required quality standards and timelines.
Deal with Sponsor generated queries in a timely manner.
Ensure the satisfactory close-out of investigator sites.
Participate, if requested, in the preparation of and review of study documentation, e.g. draft protocols, draft CRFs, monitoring guidelines and elements of final report.
Ensure correct archiving of files on completion of a study.
Co-operate with sponsor and/or QA personnel in the conduct of QA audits.
Maintain patient and sponsor confidentiality.

 
Requirements:
Cost effectiveness.

To participate in training new staff as appropriate.

Assist with marketing the company if and when appropriate.



QUALIFICATIONS/EXPERIENCE REQUIRED:

Medical/science background and relevant experience.

Ability and willingness to travel at least 50% of the time.(lnternational and domestic: fly and drive).

Ability to review and evaluate clinical data.

Computer literacy desirable.

Foreign language skills desirable.

Current full driving licence essential.

Good oral and written communication skills.



 
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Researcher 

  Immunovative Therapies Ltd.    All, Jerusalem   1/1/2008 
Category: Life Sciences  
Education: Masters   Position type: Full Time Employee  Experience: 1 year 
Area(s) of expertise desired: Cell Biology, Cell Culture, Molecular Biology  
Description:
Immunovative Therapies, Ltd. is an early stage biopharmaceutical company specializing in the development of immune cell-based therapies for cancer and infectious diseases. We are seeking a Research Associate in Jerusalem to join our team.  
Requirements:
Masters degree in cell and/or molecular biology and at least 2 years academic or industrial lab bench experience; knowledge of and experience with cell culture procedures - subculture, cryopreservation, cell counts, and staining; knowledge of biochemical and molecular biology procedures and methods, especially nucleic acids extraction, reverse transcription, quantitative polymerase chain reaction; experience with ELISA and ELISPOT assays. Knowledge of immunology helpful. Must be fluent in English.

 
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Biotechnology and Public Health 

  SKF BIOTECHS    All   10/1/2008 
Category: Biochemical  
Education: Doctorate   Position type: Full Time Manager  Experience: 3 years 
Area(s) of expertise desired: Biochemistry, Clinical Research, Microbiology, Professional Services, Quality Control  
Description:
A three-year fellowship position will be available at the Center for Drug Evaluation and Research, FDA after January 2008. This position is ideal for recent graduates with a background in Chemical Engineering, Microbiology, Virology, Biochemical Engineering, Molecular Biology, or a related field and a strong interest in the intersection of the public health and the biotechnology industry. The primary responsibilities of the position are 1) conduct a survey of current practices (bench marking) for biotechnology manufacturing unit operations to identify the key benefits and gaps in their viral clearance capacity and 2) design and conduct lab-based projects that address the most urgent gaps in viral clearance by the identified unit operations. The individual will work as part a collaborative project between CDER and Eli Lilly, Inc. The project represents an excellent opportunity for individuals to impact the direction of their research career and gain experience in an area of high industry relevance. Considerable organizational skills and the ability to work in a team are required.
For a recent basic science graduate interested in breaking into the biotechnology arena, this is a rare opportunity to work with emerging technology in the leading biotechnology regulatory agency in collaboration with a leading biotechnology firm. The position ranges from GS-9 (~$40,000/yr) to GS-11 (~$48,000/yr) equivalent depending on qualifications. A doctoral degree in Chemical Engineering, Microbiology, Virology, Biochemical Engineering, Molecular Biology, or a related field is preferred. This position requires U.S. citizenship or permanent resident status. For consideration, candidates should submit their resumes prior to Feb 15, 2008.

 
Requirements:
A doctoral degree in Chemical Engineering, Microbiology, Virology, Biochemical Engineering, Molecular Biology, or a related field is preferred. This position requires U.S. citizenship or permanent resident status.  
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CLINICAL RESEARCH ASSOCIATES (all levels) 

  Hays Pharma    All   30/9/2008 
Category: Clinical Research  
Education:   Position type: Full Time Employee  Experience: 1 year 
Area(s) of expertise desired:  
Description:
Our client, a highly reputable leading global Contract Research Organisation, is looking for Clinical Research Associates to join the team. The purpose of the role is to identify, select, initiate and close-out appropriate investigational sites for clinical studies and to monitor these sites ensuring that the studies are performed in accordance with the SOPs, applicable regulations and ICH-GCP guidelines.

ALL APPLICATIONS TO BE MADE IN ENGLISH PLEASE.

 
Requirements:
Education and qualifications

Medical/science background and 1 year previous clinical research experience;

Ability and willingness to travel at least 50% of the time;

Ability to review and evaluate clinical data;

Computer literacy desirable;

Good use of English;

Good oral and written communication skills.


 
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Computerized systems validation engineer 

  Comply    All   1/4/2015 
Category: QA - Quality Control, IT/Hardware/Software  
Education: Bachelors   Position type: Full Time  Experience: No experiece 
Area(s) of expertise desired: Business Analyst, Compliance, GLP, GMP, Information Systems, Medical Device, Other, Professional Services, Validation  
Description:
Write Computerized systems validation documents and test protocols: STP,STD,IQ,OQ,PQ
Write Computerized systems design and summary documents: URS,FRS,VP,STR,VSR
Write SOPs ( Standard Operating Procedures) , Work instructions
Write software applications reject lists, bug identification, report and monitoring.
Functional testing of life-science computerized systems.
 
Requirements:
Minimum Qualifications

Education: BA/BSC in Biotechnology, Chemical Engineering, Biomedical engineering, Chemistry, Biology, Computer Science
Communication: Excellent oral and exceptional technical writing skills with the ability to interface effectively and professionally at all levels.
Organized person with high ability to work with fine details.
Excellent English( Equal to mother tongue).
QA oriented : Experience with QA in the life-science industry( Pharma ,Biotech and Medical devices). Optional- Experience with QC in the life science industry.
Service oriented.

Preferred Qualifications

Experience with use of life science computerized system ( e.g. LIMS, ERP systems, computerized Lab systems ( Empower, FTIR etc..), production systems etc.)
Experience with IT subjects (i.e. Server- Client topology, Data backups, Help Desk etc.)
Experience in software testing\ computerized system validation in the life science industry
Knowledge in roles and guidelines: 21CFRPart11, GAMP5 ISO 14971:2007,IEC 62304
 
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CLINICAL TEAM LEAD 

  Hays Pharma    All   30/9/2008 
Category: Clinical Research  
Education:   Position type: Full Time Employee  Experience: 3 years 
Area(s) of expertise desired: Clinical Research  
Description:
An excellent opportunity has arisen to join this global Contract Research Organisation as a Clinical Team Lead.

The purpose of the role is to manage the execution of the clinical component of study protocols in accordance with the scope of work and contracted timelines.

May act as a CTL for large scale projects under the supervision of a more senior CU, or Line Manager. May also serve as a Sr Clinical Research Associate (Sr CRA) within the project or other projects as needed.

ALL APPLICATIONS TO BE MADE IN ENGLISH PLEASE.  
Requirements:
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines

In depth therapeutic and protocol knowledge as provided in company training

Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer

Strong written and verbal communication skills including good command of English language

Excellent organizational and problem-solving skills

Effective time management skills

Strong presentation skills

Effective mentoring and training skills

Ability to lead and motivate a culturally-mixed clinical team

Ability to manage competing priorities


MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Bachelors degree in a health care or other scientific discipline or educational equivalent; 3 years clinical monitoring and one year in a project leadership role or equivalent combination of education, training and experience

 
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Principal owner 

  Redwood Consulting Group, LLC    All   28/4/2008 
Category: Chemical Process Engineer  
Education: Bachelors   Position type: Full Time Employee  Experience: 8 years 
Area(s) of expertise desired: Biochemistry, Chemical Engineering, Engineering, Process Development  
Description:
Seeking a Process Engineering Associate on a Contract basis.

The position requires representing clients in bio and pharmaceutical industry in their capital projects. This translates into preparation and review of typical project deliverables, coordination between major project disciplines, operations, process development, QA, EHS, vendors/suppliers. Firm knowledge of Pharmaceutical and Biotech processes from design and operability perspective is a must.  
Requirements:
Degreed Process Engineer with 8 to 10 years of experience in pharmaceutical, biotech process design. Established knowlegde of biopharm project execution. Proven ability to generate and review process, mechanical, instrument and control deliverables. Good technical writing capability.  
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Process Engineering Associate on a Contract basis. 

  Redwood Consulting Group, LLC    All, Richboro   28/4/2008 
Category: Biotechnology, Pharmaceiuticals  
Education:   Position type: Full Time Employee  Experience: 9 years 
Area(s) of expertise desired: Chemical Engineering  
Description:
The position requires representing clients in bio and pharmaceutical industry in their capital projects. This translates into preparation and review of typical project deliverables, coordination between major project disciplines, operations, process development, QA, EHS, vendors/suppliers. Firm knowledge of Pharmaceutical and Biotech processes from design and operability perspective is a must.  
Requirements:
Degreed Process Engineer with 8 to 10 years of experience in pharmaceutical, biotech process design. Established knowlegde of biopharm project execution. Proven ability to generate and review process, mechanical, instrument and control deliverables. Good technical writing capability.  
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Senior CRA 

  Hays Pharma    All   18/6/2008 
Category: Life Sciences  
Education: Bachelors   Position type: Full Time Team Leader  Experience: 3 years 
Area(s) of expertise desired: Clinical Research, Gastroentology  
Description:
As a Senior Clinical Research Associate you would perform trial initiation, close out activities, you would coordinate monitoring activities, manage site activities to ensure clinical data integrity in line with company Regulatory and Ethical guidelines for Good Clinical Practice. You would provide clinical and technical support and would develop CRFs and act as liaison between monitoring and other functions.You would also operate as the focus for communication with Clinical Research Associates and the Sponsor. You would also act as the lead contact of the project team with study site personnel and also act as a mentor for CRAs. As you would report to the project leader and may assume the role of Lead CRA by providing direction to the project team.  
Requirements:
-Experience as a Clinical Research Associate
-Co-ordination skills
-Experienced in conducting allocated tasks
-Maintain up-to-date knowledge of ICH-GCP, EU CT Directive and FDA guidelines
 
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