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| Novartis Oncology |
na |
CA |
7/31/2010
|
| Development Scientist |
| * Bachelor's degree in science or engineering discipline or similar
* Fluent in speaking / writing in English
? 1-3 years experience in pharmaceutical/biotech with production in a GMP facility
? Demonstrated experience and competencies in fermentation and protein recovery or protein recovery and purification
? Ability to manage smaller projects
? Ability to handle multiple projects simultaneously under tight deadlines
? Working knowledge of Good Laboratory/Manufacturing Practices, regulations, regulatory compliance requirements and current industry standards
? Strong verbal and written communication skills |
| Novartis Oncology |
na |
MA |
7/31/2010
|
| Biobanking Project Manager |
| PhD, or PharmD
Languages: Fluent English (verbal and written)
Experience of min. 2+ years pharmaceutical or biotech industry experience. Previous experience in a multi-disciplinary environment.
Knowledge of translational/clinical science.
Understanding of the drug development process.
Laboratory experience in handling biological samples and biomarker analysis.
Team player with demonstrated ability to build collaborative relationships.
Strong interpersonal and communcation skills for managing timelines, budget and resources and for effective internal collaboration.
Excellent verbal and written communication skills.
Expertise in Microsoft Office, Microsoft Sharepoint, and Lotus Notes are necessary. |
| Novartis Oncology |
na |
NJ |
7/31/2010
|
| Research Investigator, Preclinical Imaging, Investigative Toxicology |
| ? Ph.D. degree in Biochemistry, Physiology, Pharmacology, Toxicology, Biophysics, Biomedical Engineering or related field in the biomedical sciences
? At least 2 years of prior experience in pharmaceutical drug development and/or toxicological sciences required.
? Experience with hands-on in vivo small animal imaging, preferably with multiple imaging modalities. A strong expertise in small animal (rat, mouse) Ultrasound imaging for various applications including contrast enhanced ultrasonography is preferred.
? Expertise and knowledge in vascular toxcology and in vitro vascular ring assay would be a plus.
? Experience of managing highly skilled technical staff, laboratory equipment, consumables and safety is desirable.
? Fluency in English (written and spoken) is a must
? Flexibility and ability to work in a team, comfortable with multitasking, excellent interpersonal skills to communicate and collaborate within a multi-disciplinary environment, willingness to take on additional responsibilities are expected
? Excellent project management skills
Technical Skill Requirements:
? Experience with pre-clinical applications of MR imaging and spectroscopy, X-ray microCT, ultrasound and/or optical imaging
? Imaging data processing and analysis |
| Novartis Oncology |
na |
GA |
7/31/2010
|
| Quality Control Analytical Lab Supervisor |
| Minimum Education and Experience Requirements:
Requires a Bachelors degree in Chemistry or related science from and accredited college or university with a minimum of 7 years of experience overall with 5 years supervisory experience in a regulated laboratory, preferably in a pharmaceutical laboratory environment.
Requires solid knowledge of quality control systems, including FDA compliance standards, regulations, and guidelines.
Requires excellent oral and written communication, organizational and teamwork skills.
n equivalent combination of education, experience and training may substitute.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
7/31/2010
|
| Molecular Histologist |
| Applicants should hold a MS degree or have equivalent experience in biology (or related fields) with 5 plus years experience as research histologist in the bio-pharmaceutical industry. An excellent understanding and practical experience of special histology techniques and immunohistochemistry applied to pre-clinical research is essential. Excellent knowledge of molecular biology concepts and bioinformatics tools applicable to research histology in order to select appropriate reagents and assay design is highly desirable. Previous experience in digital slide scanning and image analysis applied to tissue sections is also required. Experience in confocal microscopy is a plus. Excellent organizational skills and project planning in daily laboratory activities are essential. Good interpersonal skills and experience in coordination of daily laboratory work is also highly desirable. Excellent computer skills with daily experience with Microsoft Office environment are also required. |
| Novartis Oncology |
na |
MA |
7/31/2010
|
| Molecular Phenotyping Scientist |
| Applicants should hold a BS degree in biology (or related fields) with 2 plus years experience as research histologist in the bio-pharmaceutical industry or biomedical research. A very good understanding and practical experience of special histology techniques and immunohistochemistry applied to pre-clinical research is essential. Excellent knowledge of molecular biology concepts applicable to research histology in order to select appropriate reagents and assay design is highly desirable. An excellent capacity and adaptability to learn new techniques under the direction of more senior laboratory peers is required. Previous experience in digital slide scanning and image analysis applied to tissue sections is a plus. Excellent organizational skills in daily laboratory activities are essential. Good interpersonal skills and capacity to conduct laboratory activities in a dynamic cross-functional research environment is essential. Excellent computer skills with daily experience with Microsoft Office environment are also required. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
7/30/2010
|
| Medical Director, Medical Sciences- Oncology |
| M.D. degree, Board Certified or Board Eligible in Oncology/Hematology.Minimum three years clinical experienceMinimum two years laboratory or clinical research experience and five years experience in the pharmaceutical industry or equivalent academic experience.Knowledge of regulatory procedures and guidelines (preferably global)Experience in clinical development, preferably experience in at least 2 phases Effective team player in a matrixed R&D environmentAble to work independently on all aspects of assigned projectsExcellent presentation and writing skillsExcellent organizational skills |
| Vertex Pharmaceuticals |
Cambridge |
MA |
7/30/2010
|
| Temp QA Specialist |
| * B.S (or equivalent degree) and 3-5 years of relevant work experience
* Experience with analytical testing and data review in a GMP environment.
* Experience with the following analytical techniques desirable; HPLC, GC, Dissolution, KF moisture, TGA, FTIR, NMR, UV, wet chemistry. (With emphasis on HPLC and GC experience)
* Reference standard testing.
* Non-conformance or laboratory investigation experience.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
NJ |
7/31/2010
|
| Principal Scientist - Salt and Polymorphism Expert |
| Education (minimum/desirable):
Minimum: BS/MS organic/analytical chemistry with 7-10 years of experience in solid state chemistry of APIs.
Desirable: Ph.D. organic/analytical chemistry or equivalent education with strong emphasis on solid state chemistry with 3-5 years of experience in pharmaceutical industry (knowledge of molecular modeling and GMPs would be a plus). Experience with form selection, polymorphism, and physicochemical characterization of APIs. Familiarity with current analytical instrumentation and techniques to characterize API forms using FBRM, XRPD, DSC, TGA, vibrational spectroscopy, UV-Vis, vapor sorption, GC, HPLC, size and solubility measurement, with an emphasis on laboratory automation. Excellent written and verbal communication skills. Good project management, time management, and decision making skills.
Languages: Fluent English (oral and written)
Experience/Professional requirement:
1. Successfully demonstrated several years (minimum of 3 years)of directly related experience as senior scientist or equivalent in pharmaceutical R&D.
2. Documented scientific/technical expertise in form selection, polymorphism, and characterization of APIs.
3. Successfully demonstrated track record of creativity and problem solving in projects.
4. Proven track record in utilization of special tools/equipment, lab automation tools and specialized facilities.
5. Profound literature search skills.
6. Strong presentation skills and scientific/technical writing skills.
7. Proven scientific leadership skills.
8. Ability to work in interdisciplinary teams.
9. Familiarity with the current analytical instrumentation and techniques to characterize crystalline and amorphous materials.
10. Familiarity with GLPs as applied to pharmaceutical industry. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
7/30/2010
|
| Research Associate, Antibody Drug Conjugates - Agensys, Santa Monica, CA |
| BS/MS degree in biochemistry, biophysics, molecular biology or related field. Must have 3 plus years of experience within the pharmaceutical industry or relevant academic experience. Prior experience in a research laboratory engaging in antibody purification and characterization is required. Experience with chromatography and HPLC is preferred. Familiarity with conjugation and crosslinking chemistries will be a plus. Must be detail oriented and able to handle multiple tasks efficiently. |
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