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Job Search Results: Jobs 1 - 10 of 187  View Titles Only  Page 1 of 19
 
Title   Company Name     Location   Date  
Manufacturing 

  Fellen Project    All   2/8/2007 
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: Masters   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Manufacturing/Production  
Description:
Our client, a manufacturing company. has an immediate opening for cost accountant with 4-year accounting degree and a minimum of 2-4 years experience in a manufacturing process cost environment. Responsibilities include preparation of manufacturing budgets, month-end close, standard cost and variance analysis, financial analysis, and inventory reconciliation. The successful candidate should have the ability to work with various levels of management and a working knowledge of Microsoft Excel. JD Edwards or other MRP package experience preferred. Salary 45-55K. DOE  
Requirements:
Our client, a manufacturing company. has an immediate opening for cost accountant with 4-year accounting degree and a minimum of 2-4 years experience in a manufacturing process cost environment. Responsibilities include preparation of manufacturing budgets, month-end close, standard cost and variance analysis, financial analysis, and inventory reconciliation. The successful candidate should have the ability to work with various levels of management and a working knowledge of Microsoft Excel. JD Edwards or other MRP package experience preferred. Salary 45-55K. DOE  
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CRA II - Israel 

  Hays Pharma    All   22/8/2007 
Category: Clinical Research  
Education: Bachelors   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Biology, Cardiology, Clinical Research, Communications, Compliance, Dermatology, Endocrinology, Gastroentology, Gynecology, Immunology, Infectious Disease, Nephrology, Neurology, Oncology, Operations, Ophthalmology, Pharmacology, Radiology, Urology, Virology  
Description:
Identify, select, initiate and close-out appropriate investigational sites for clinical studies.

Monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with Company's SOPs/WPs applicable regulations and the principles of ICH-GCP.

Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues.
 
Requirements:
Knowledge of Company's Clinical Research SOPs/WPs, ICH-GCP and appropriate regulations.

Knowledge of Company's systems

Recruitment of investigators.

Independent and proactive coordination of all the necessary activities required to set up and monitor a study, including but not limited to the following:
Identify investigators.
Help when requested, in preparation of regulatory submissions.
Design of patient information sheets and consent forms.
Coordinate documents translation, verification and back translations where required.
Ensure timely submission of protocol/consent/Safety reports documents for ethics/IRB approval.
Pre-study and initiation visits.
Conduct regular monitoring visits in accordance with our client's site monitoring SOP/Sponsor site monitoring SOP/WP, 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 regularly informed.
Process case record forms to the required quality standards and timelines.
Deal with Sponsor generated queries in a timely manner.
Participate in feasibility studies for new proposals, as required
Ensure the satisfactory close-out of investigator sites.
Act in a Lead role on a study, assuming additional responsibilities as detailed/documented by the Clinical Project Manager (CPM), if appropriate.
Ensure correct archiving of files on completion of a study.
Maintain patient and sponsor confidentiality.
Assume additional responsibilities as directed by Associate Clinical Project Manager/CPM/Clinical Project Director.

To be cost effective.

Participate in mentoring new staff.

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 (international 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.

HAYS Pharma provides extensive resourcing solutions to the pharmaceutical industry. Having established relationships with the world`s leading organisations within Pharmaceutical / Biotech / Clinical Research / Consulting industries our consultants are ideally placed to provide our candidates with their next best career opportunity.

Services advertised by Hays Pharma are those on an Agency and/or an Employment Business.

 
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CRA - International Company - Israel 

  Hays Pharma    All   22/8/2007 
Category: Clinical Research  
Education: Bachelors   Position type: Full Time Employee  Experience: 1 year 
Area(s) of expertise desired: Biology, Cardiology, Chemistry, Clinical Research, Endocrinology, Gastroentology, Gynecology, Immunology, Infectious Disease, Internal Medicine, Nephrology, Neurology, Oncology, Ophthalmology, Pharmacology, Urology, Virology  
Description:
Identify, select, initiate and close-out appropriate investigational sites for clinical studies. To monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with our client's SOPs/WPs, applicable regulations and the principles of ICH -GCP.  
Requirements:
Familiarity with Companys' Clinical Research SOPs/WPs, ICH-GCP and appropriate regulations.

Familiarity with Company's Systems

Familiarity with principles of investigator recruitment.

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.
Coordinate documents translation, verification and back translations where required.
Ensure timely submission of protocol/consent documents/safety reports for Ethics/IRB approval according to local requirements.
Pre-study and initiation visits.
Conduct regular monitoring visits in accordance with our client's site monitoring SOP/Sponsor site monitoring SOP/WP, 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 regularly 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.
Ensure correct archiving of files on completion of a study.
Co-operate with sponsor and/or Company's QA personnel in the conduct of QA audits.
Participate in feasibility studies for new proposals, as required
Maintain patient and sponsor confidentiality.
To be cost effective
To participate in mentoring of new staff up to Clinical Research Associate level 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 (international 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.

HAYS Pharma provides extensive resourcing solutions to the pharmaceutical industry. Having established relationships with the world`s leading organisations within Pharmaceutical / Biotech / Clinical Research / Consulting industries our consultants are ideally placed to provide our candidates with their next best career opportunity.

Services advertised by Hays Pharma are those on an Agency and/or an Employment Business.



 
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Operation Deputy Manager 

  confidential    All, Rehovot   26/12/2011 
Category: Biotechnology, Engineering, Chemistry, Life Sciences,  
Education:   Position type: Full Time Team Leader  Experience:  
Area(s) of expertise desired:  
Description:
The position includes: production of company products
Maintaining and co-managing the pilot plant
Managing as well as " hand" working
the job is for Rehovot and Hedera  
Requirements:
Relevant education- Engineer/practical Engineering degree or technologist in the fields of Chemistry/food/ Biotech/engineering or first degree (Bsc) in Biotechnology
Ability for intensive and hard work and unusuall working times
wanted yet not obligated:
previous experience in producing of plant extracts; work with mechanical manufacturing devices, such as centrifuges; reactors; filtration equipment and clean room work
background and experience in food or biotechnology industry  
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manager 

  larry bee    All, chicago   15/3/2012 
Category: QA - Quality Control, IT/Hardware/Software  
Education: Masters   Position type: Full Time Manager  Experience: 6 years 
Area(s) of expertise desired: Academic  
Description:
A management consulting firm, we are focused exclusively on the metals industry. Our objectives are to identify opportunities for clients to reduce the cost of new metal, improve the value received for scrap, manage price risk exposure and strengthen administrative and financial controls.  
Requirements:
A management consulting firm, we are focused exclusively on the metals industry. Our objectives are to identify opportunities for clients to reduce the cost of new metal, improve the value received for scrap, manage price risk exposure and strengthen administrative and financial controls.  
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Clinical Study Manager 

  Hays Pharma    All   18/6/2008 
Category: Life Sciences, Clinical Research  
Education: Bachelors   Position type: Full Time Team Leader  Experience: 8 years 
Area(s) of expertise desired: Clinical Research  
Description:
Our client, a global Clinical Research Organization is seeking an experienced Clinical Study Manager to join their successful team.

Qualifications

Proven track record in study management, who possess well developed communications skills, and who will enjoy working with team. Your expertise as a Study Manager of International trials will ensure that clinical stages of research projects are completed efficiently and in accordance with customer expectations, enabling us to continue our success.

The successful candidate will have a degree, or equivalent, in a scientific or healthcare discipline complemented by solid international study management experience as a Clinical Study Manager for large scale cross-regional or International trials and previous experience as a successful and accomplished Clinical Research Associate

This role involves managing the execution of the clinical component of large, complex study protocols or global projects in accordance with the scope of work, contracted timelines and study budget. This involves the management of clinical study set-up through to the ongoing tracking and review of the study progress and reporting to relevant members of senior management.

Responsibilities

- Collaborate with other functional groups within the company such as data management, pharmacovigilance, and biostatistics where necessary to support milestone achievement and to manage study issues and obstacles.
- Provide ongoing training and support to the clinical team, including the mentoring of less experienced Clinical Team Leaders. Establish study tools and training materials. Conduct frequent team meetings and ensure regular communication.
- Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site visits and ongoing mentoring of CRA team.
- Develop the risk management plan from a clinical perspective and coordinate clinical issue escalation and resolution with the Project Manager. Develop proactive contingency plans to mitigate clinical risk.
- Identify quality issues within the study through regular review of the clinical team communications including site communications, monitoring visit reports, data flow information and quality assurance audit findings. Implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties.
 
Requirements:
Requirements

- In depth knowledge of, and skills in applying, applicable clinical research regulatory requirements
- Bachelor's degree in a health care or other scientific discipline or educational equivalent
- significant experience working on clinical trials including monitoring as well as previous experience in a project leadership role with expanding cross-regional/global focus
 
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Extra Money in a new Sales Project 

  Con    All   23/5/2012 
Category: Biotechnology, Chemistry, Life Sciences, Pharmacy/Pharmacology, Healthcare, Sales/Marketing  
Education:   Position type: Full Time Employee  Experience: No experiece 
Area(s) of expertise desired:  
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  
Requirements:
Please send CV to: project@slimail.com  
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Clinical Project Manager 

  CRO    All, ISRAEL   8/8/2007 
Category: Clinical Research- Pharma-Biotech  
Education: Bachelors   Position type: Full Time Manager  Experience: 3 years 
Area(s) of expertise desired: Business Development, Clinical Research, Project Management  
Description:
To manage clinical studies
To ensure that studies are performed and completed in accordance with the pre-defined budget, timelines and quality specifications
To ensure that a safety reporting system is in place and that safety reports are provided to the Safety Department in a time manner
To ensure that studies are conducted in accordance with GCP requirements and relevant company SOPs
Main contact with Local Regualtory Authorities.  
Requirements:
Bachelor's degree in a health care or other scientific equivalent;
Experience working on clinical trials for at least 3 years;
In depth knowledge of applicable clinical research requirements;
Strong written and verbal communication skills including good command of English language;
Computer skills including Microsoft Word, Excel and PowerPoint;
Excellent communication, organizational and problem-solving skills;
Effective mentoring, communication and training 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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management 

  collins ind ltd    All   28/11/2007 
Category: Management/Executive  
Education:   Position type: Full Time  Experience:  
Area(s) of expertise desired: Engineering  
Description:
Well my company is very big and i want workers to work in my company now.  
Requirements:
Well my company is very big and i want workers to work in my company now.  
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