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To organize and carry out the training of new staff To direct and perform fungal and bacterial analysis
To manage the availability of staff, equipment and consumables within the laboratory, thus ensuring that all the work can be completed appropriately.
To ensure that staff resource is suitably split within the laboratory to enable all work to be completed as required.
To ensure that training protocols are suitably implemented within the laboratory to provide a balanced (but increasing) level of competency within all analytical areas.
To provide sound Microbiological advise to the R&D team.
To ensure compliance with all the internal and external quality systems
To prepare, review and implement SOPs
Requirements:
Degree in Medical Technology, Clinical Lab Science, or related science (Microbiology, Biology etc.)
8+ years experience working in a laboratory environment (preferred both clinical and research)
3+ years experience of supervising staff.
Qualified microbiology lab managing
Experience of working in a regulated environment.
Strong background in bacteriology
The ability to work accurately under pressure
A good standard of verbal and written communication
Good computer skills
Fluent English (read and speak)
The position is responsible for planning and coordination of product change strategies across the network to achieve business goals. This includes project management oversight of commercial product technology and/or volume transfers, and product, material, and process changes, with a regional and/or technology focus. Lead and inspire diverse teams to meet project goals
Requirements:
Requirements:
Education: Bachelor's degree in a technical or scientific discipline. An advanced degree in a related field or MBA is highly desirable; Project Management certification is a definite plus
Experience: 5+ years of experience in Supply Chain, Operations, Quality, and/or Regulatory, etc. with increasing levels of responsibility in a pharmaceutical or other regulated environment. Experience in project management of multiple complex projects simultaneously
Experience with MRP, SCM, ERP systems and Microsoft platform applications (MS Word, Excel, Powerpoint, MS Project); Cognos or other data analysis tools
This position is based in Petach Tikva, with up to 25 % domestic or international travel
הגשת מועמדות למשרה באמצעות הלינק הבא:
http://careersisrael.tevapharm.com/job2433
PhD position available at the Pharmacogenetics and Translation Medicine Center at Technion, Haifa Israel in Prof. Ariel Miller group
We are looking for a PhD student for a novel and challenging project entitle Genetic and Epigenetic factors in Myasthenia Gravis. The project will combine bench-work, large data-set analysis, genetics association study, and bioinformatics. Basic genetics knowledge required, computer and analytical skill desirable.
our company is engaged with anti cancer drug development and we are looking for a part time employee to be resposible for the regulatory affairs of the company BUT not a consultant
Requirements:
b"h
we ask a regulatory person with 1-2 years of experience of work in the field that can work with our regulatory consultant
1. Over 45 years old
2. planning and creativity abilities
3. 12 years experiance in Electronic development
4. prefferable power suppliers and RF developers
5. Work place in Petah-Tikva
6. working hours 08:00-17:00 without Fridays
Formulation, Internal Medicine, Medical Tech, Pharmacology, Professional Services, Start-Up
Description:
A Biotech Start-up company
Is seeking
A Medical Director
Requirements:
- Israeli license to practice medicine
- Internal doctor – a plus
- At least 4 years of experience in drug development
- Part time job in Jerusalem
- Mother-tongue level English
Biotechnology, Chemistry, Life Sciences, Pharmacy/Pharmacology, manager
Education:
Doctorate
Position type:
Full Time Manager
Experience:
3 years
Area(s) of expertise desired:
Academic, Biochemistry, Chemistry, Protein Chemistry, Proteomics, protein purification
Description:
Job Description:
Lead, design, develop and optimize purification processes for recombinant proteins as human therapeutics. Lead and manage the development of in-process control methods, characterization studies that evaluate percent recovery, consistency, purity, and stability of selected protein candidates. Industrial experience with techniques including different chromatographic methods, HPLC, SDS-PAGE, western blot, and ELISA is essential.
Requirements:
Preferred Qualifications:
Applicants should have a Ph.D. degree in Biological Sciences or Chemistry and demonstrated experience in the Biotech industry with development of purification processes for recombinant proteins, preferably with managerial experience. Applicants must have profound theoretical knowledge of protein chemistry, be able to independently design integrated purification processes for a variety of proteins, supervise the operation of relevant equipment and have experience with a variety of chromatographic and separation techniques. Applicants must be task oriented, perform in a dynamic work environment where objectives can change and deadlines are critical. Excellent communication, teamwork and training skills are essential. Applicants must be fluent in English with strong ability to produce technical and scientific reports and documentation.
