| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Principal Scientist I - Preformulation/Formulation Group Leader |
|
| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Validation Engineer I |
|
| Agilent Technologies, Inc. US |
Chandler |
AZ |
9/4/2010
|
| Sales - Genomics Product Specialist |
| - Minimum BS/MS in Chemistry or a Life Sciences discipline, or equivalent.
- Solid self management and organizational and prioritization skills
- 5+ years related direct sales experience with a demonstrated track record of successfully selling against a quota.
- High level of experience in microarrays and/or NGS.
- Technical knowledge and domain knowledge in the research and diagnostic sector of the pharmaceutical industry (profit and not for profit. Knowledge of the cytogenetics market.
- Industry/Application expertise. Working knowledge of competitive products (specifications, value propositions, price points).
- Comfortable interfacing with senior managers within your customers.
- Demonstrated commercial selling skills. Strong business development and sales closing skills.
- Effective interpersonal communication and telephone sales skills.
- Must be able to travel up to 35% of the time.
Geo Location: Arizona (preferred) or Texas |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Software Engineer |
| * Bachelors or Masters degree in computer science and/or physical science.
* More than 5 years experience in industry-related software development
* Experience in the following software fields
- Application development experience using Oracle and SQL databases and Schema Design
- Windows development using .NET, C#, and C++
- Experience with Windows Services, WCF, Web Services
- Experience in server side development
- Desired experience in MVVM & CAL, MSI, MSBuild and WIX
- Also desired are experiences in Search Technologies, Data Object Design and Data Warehousing |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Software Engineer |
| Job Requirements:
? Strong C# programming experience.
? Experience using Microsoft Visual Studio and source management tools, such as Microsoft Team Foundation Server.
? Experience using DevExpress, WPF, or similar GUI toolset.
? Broad knowledge and experience using design patterns.
? Strong work ethic with focus on quality, follow-through, and attention to detail.
? Good communication skills.
? Experience synthesizing a cohesive system consisting of hardware, electronics, firmware, and software.
Education & Experience:
? Degree in computer science, engineering, or related field.
? 5+ years of technical experience.
? Experience developing production quality software.
? Experience with C++ desired.
? Experience with TCP/IP desired.
? Experience with embedded programming desired. |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
9/4/2010
|
| Field Service Engineer- Los Angeles Area |
| Requires BS or MS Degree or equivalent and 3 or more year's relevant experience with the use,repair,troubleshooting of hardware, software applications support and routine preventative maintenance, qualification and verification of Agilent's Liquid Chromatographs and LC Mass Spectrometers. LCMS experience required.
Geographic Location: Los Angeles Area
Agilent will not sponsor work authorization for this position |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Bioinformatics, Senior Software Engineer |
| External Qualifications:
This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines.
Chosen candidate must have the following:
? 5+ years experience in C++, .NET, and Java
? Object oriented programming experience a plus
? Experience with: BLAST, BLAT and/or MOST
? Experience with SQL and/or Oracle database
? Knowledge of public biological databases, tools, and repositories is required
? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable
? Experience with Image Analysis is a plus
Geographic Location: Bay Area, California (Santa Clara) |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Bioinformatics, Software Engineer |
| External Qualifications:
This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines.
Chosen candidate must have the following:
? 2+ years of experience in providing bioinformatics solution in next gen sequencing space.
? 5+ years experience in C++, .NET, and Java
? Object oriented programming experience a plus
? Experience with: BLAST, BLAT and/or MOST
? Experience with SQL and/or Oracle database
? Knowledge of public biological databases, tools, and repositories is required
? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable
? Experience with Image Analysis is a plus
Geographic Location: Bay Area, California (Santa Clara) |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Sr.Engineer/Ass. Staff Engineer |
| B.S. degree in physics, chemistry, or electrical engineering or equivalent, plus a minimum of 7 years of related experience, or an equivalent combination of M.S or Ph.D. degree and experience. Advanced degree and minimum of 6 years of relevant experience required for Staff Engineer.
*NMR experience, NMR systems experience and good operating knowledge of VNMRJ are strongly preferred.
*Good RF, analog, and digital electronic experience and operation of related test equipment required. And/or experience with High Powered RF preferred
*Mechanical engineering and machine shop experience a plus.
*Unix/Linux operating knowledge, basic CAD experience, and knowledge of MS Office required.
Strong analytical and troubleshooting skills are required.
*Good verbal and written communications skills. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Production Manager |
| This is a managerial position for NMR Cold Probe Production and NPI. The manager is responsible for overseeing the assembly and test of all production cold probes, and coordinating closely with development on specials. The manager will also be responsible for working closely with Cold Probe Development on the smooth introduction of new products into production.
List Minimum education, training and experience needed to perform this job:
1. 15 years experience with NMR probes
2. 5 years minimum supervisory experience
3. familiarity with cryogenic and vacuum systems
4. 10 years manufacturing/production engineer experience |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| R&D FPGA Engineer |
| Key required skills:
? Bachelors or Masters Degree or University Degree in Electrical Engineering and 5+ years applicable experience in FPGA design
? Ability to use FPGA simulation and design tools to realize and verify high quality and robust solutions in Verilog or VHDL.
? Experience with Xilinx ISE, including Plan Ahead, and synthesis tools, such as Synplify
? Ability to perform characterization and testing of design prototypes, and analyze and validate the design to meet product performance specifications.
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Desired skills:
? Educational emphasis or work experience with signal processing theory, applications and development
? Skills in signal processing algorithm development and implementation using FPGAs
? Experience with team-based FPGA development ? design partitioning and integration
? Knowledge in high-speed digital design, PCI Express, DMA, memory systems |
| Agilent Technologies, Inc. US |
Everett |
WA |
9/4/2010
|
| R&D Signal Processing Software Engineer |
| Key Required Skills:
? Bachelors or Masters Degree or University Degree in Electrical Engineering or Computer Science
? Must have 5+ years applicable experience in software development involving signal processing theory, techniques and algorithm development
? Must have experience with the use of computer tools for simulation
? Must have demonstrated proficiency with C/C++ or C# programming languages
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Additional Desired Skills:
? Proficiency with C#,.Net, Visual Studio, defect tracking, revision control, real-time systems and software/firmware lifecycles. |
| Agilent Technologies, Inc. US |
Everett |
WA |
9/4/2010
|
| R&D Hardware Control Software Engineer |
| This is a key SW development role.
Key Required Skills:
? Bachelors or Masters Degree in Electrical Engineering or Computer Science
? 3+ years applicable experience in software development involving hardware control and IO
? Must have proficiency with C#, C++, .Net, Visual Studio, defect tracking, revision control and software/firmware lifecycles
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Additional Desired Skills:
? Familiarity with Windows device drivers
? Experience with the Windows Presentation Foundation graphical subsystem
? Educational emphasis or work experience with signal processing theory, applications and development |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Manufacturing Operations Coordinator |
| Musts:
- Demonstrated ability to work in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated ability to read and understand written procedures and instructions.
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures).
- Demonstrated ability to make timely decisions.
- Experience with troubleshooting and applying corrective actions.
- Demonstrated ability to maintain accurate records.
- Experience working with computers: keyboarding, Windows environment.
- Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- May be required to lift materials per entity specified and approved limits.
- May be required to participate in medical/screening or monitoring programs.
Desired:
- Basic PC skills: spreadsheets, word processing, databases.
- Previous manufacturing experience in an ISO certified environment. |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Manufacturing Operations Coordinator |
| Musts:
- Demonstrated ability to work in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated ability to read and understand written procedures and instructions.
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures).
- Demonstrated ability to make timely decisions.
- Experience with troubleshooting and applying corrective actions.
- Demonstrated ability to maintain accurate records.
- Experience working with computers: keyboarding, Windows environment.
- Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- May be required to lift materials per entity specified and approved limits.
- May be required to participate in medical/screening or monitoring programs.
Desired:
- Basic PC skills: spreadsheets, word processing, databases.
- Previous manufacturing experience in an ISO certified environment. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D engineer |
| Qualifications:
- Bachelor/Master/PhD Degree in Electrical/Electronic/Computer Engineering with >5 years related working experience
- Experience with Xilinx ISE, ModelSim, Synplify
- Experience with VHDL or Verilog
- Experience using equipment like oscilloscopes and logic analyzers for problem resolution and design verification
You will be measured on:
Technical capability and competence and ability to grow and remain technically current
Creativity in designing applicable solutions
Ability to work with a team to deliver results as committed |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Hardware Engineer |
| Qualifications:
- Bachelor/Master/PhD Degree in Electrical/Electronic/Computer Engineering with >3 years related working experience
- Knowledgeable in PCIe/modular busses, high-speed digital and memory systems, power integrity, thermal management
- Strong knowledge of digital design with emphasis on ASICs or Xilinx FPGAs
Desired:
- Nano technology/surface science or instrumentation measurement science/domain knowledge
- Strong knowledge of digital and analog hardware, FPGA or digital ASIC development principles, Verilog or VHDL, synthesis, and simulation tools.
- Knowledge of Xilinx ISE, Plan Ahead
- Knowledge of distributed clocking schemes
You will be measured on:
Technical capability and competence and ability to grow and remain technically current
Creativity in designing applicable solutions
Ability to work with a team to deliver results as committed |
| Agilent Technologies, Inc. US |
Albuquerque |
NM |
9/4/2010
|
| Field Service Engineer- Albuquerque |
| Requires BS or MS Degree or equivalent and 2 or more years relevant experience with the use, repair, routine preventative maintenance, qualification and verification of Agilent LSCA products including GC Mass Spectrometers, Gas Chromatographs, Liquid Chromatographs,GC Headspace, and Chemstation Data Systems.
Must have GC and GCMS experience.
Desired LC and ICPMS experience
Geographic Location: Albuquerque, New Mexico |
| Agilent Technologies, Inc. US |
Indianapolis |
IN |
9/4/2010
|
| Product Specialist - Columns and Supplies - Midwest |
| - BS Degree in Science (Chemistry/Biology) or equivalent
- 8+ years progressive experience in chromatography applications and/or sales along with a demonstrated track record of results preferred.
- Proven ability to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities.
- Ability to solve a broad range of problems of varying scope and complexity.
- Excellent communication and teamwork skills is a must.
Geo Location: Midwest Area |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Material Coordinator-2nd shift |
| May require some higher education or specialized training/certification.
Requires a minimum of 3 years directly related experience, with typically 4 to 6 years' experience.
Musts:
- Demonstrated ability to work in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated ability to read and understand written procedures and instructions.
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures).
- Demonstrated ability to make timely decisions.
- Demonstrated ability to maintain accurate records.
- Experience working with computers: keyboarding, Windows environment, spreadsheets, word processing, databases.
- Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- Required to lift materials per entity specified and approved limits.
- May be required to participate in medical/screening or monitoring programs.
Desired:
- Previous experience using SAP in a material coordination capacity.
- Previous manufacturing experience in an ISO certified environment |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Product Manager / Life Sciences Marketing |
| ? 5+ years of product marketing/management experience; services marketing experience a plus
? Familiarity with Life Sciences industry and analytical instrumentation
? Track record of successful business results
? Bachelors degree in chemistry, biology or related scientific field or equivalent; MBA a plus
? Experience in leading cross-functional and international project teams
? Excellent verbal and communication skills
? Ability to travel, including international, approximately 35% of the time
? Physical work location at a major Agilent site (Santa Clara, CA or Wilmington, DE or Englewood, CO) strongly preferred |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Product Manager |
| ? Minimum bachelors degree in chemistry, biology or related scientific field or equivalent; MBA a plus
? Minimum 4 years of product marketing experience; strong preference for Services Marketing experience
? Minimum of 3 years experience in marketing, selling, commercializing, managing, supporting analytical lab instrumentation or analytical lab experience, preferably in the Life Sciences industry
? Track record of business results
? Strong evidence of customer orientation
? Demonstrated ability to influence all levels of an organization, across regional/cultural boundaries and across multiple disciplines
? Excellent verbal & written communication skills.
? Ability to travel, including international
(10-30%)
Location: In Santa Clara, CA, Wilmington, DE, Englewood, CO |
| Agilent Technologies, Inc. US |
Tigard |
OR |
9/4/2010
|
| Account Manager |
| Bachelors or Master Degree in engineering (Electrical Engineering is a plus) and a minimum of 5+ years as a strategic Account Manager
Experience selling digital & wireless test products
Strong knowledge and Experience dealing with customers in the computer, wireless, and data networking industries
The candidate must live in close proximity to Portland, Oregon |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Mixed-Signal/RF IC Designer |
| Education:
Ph.D. in Electrical Engineering or closely related field with thesis work on mixed-signal IC design preferred. Candidates should have designed, have had fabricated and characterized a mixed-signal or RF integrated circuit as a central portion of their relevant thesis work.
M.S. in Electrical Engineering with experience in or substantial coursework related to mixed-signal IC design required. Candidates not possessing a Ph.D. degree must have completed the design, have had fabricated and characterized a mixed-signal or RF integrated circuit of complexity and performance commensurate with that of a Ph.D. thesis. In addition, two years relevant full-time employment experience or full-time graduate study is required post M.S. degree.
Qualifications:
Must have experience in the design of high-speed analog, mixed-signal or RF integrated circuits.
Substantial involvement in the design of transistor level circuits for inclusion on an IC, physical design of ICs, and the test and characterization of an IC.
Strong understanding of transistor physics and EM theory and their impact on circuits. Experience in 2-D and 3-D electromagnetic simulation of on-chip structures and derivation of a model for use in circuit simulators is highly desired.
Ability to synthesize multiple solutions to a given problem and the ability to critically analyze the strengths and weaknesses of each.
Experience with modern EDA tools used in IC design including simulation, schematic capture, physical layout and verification.
Familiarity with programming and scripting languages to enable automation in the design, simulation and testing of ICs.
Demonstrated ability to work well in a team environment is a must. Ability to document and present results.
Preferred Qualifications:
Experience with the use of both sub-micron CMOS and modern SiGe bipolar devices (fT > 150 GHz) in analog, mixed-signal, or RF integrated circuit design.
Experience with PLLs, clock-data recovery circuits, and data converters.
Experience with custom high-speed digital data paths.
Experience with a synthesized digital design flow, from a high-level HDL to transistor level artwork.
Experience with mixed-mode simulation of analog and digital blocks -- mixed-signal or behavioral modeling of analog circuits.
Experience with device modeling, thermal design, IC package design. |
| Agilent Technologies, Inc. US |
Cary |
NC |
9/4/2010
|
| Production Manufacturing Supervisor |
| ? Will have a bachelor?s degree in a technical or operational field.
? Will have a minimum of five years of experience as supervisor preferably in high precision technology product manufacturing.
? Extensive knowledge of lean manufacturing process activities and quality management system requirements.
? Proficiency with SAP or other ERP systems and Microsoft Office Applications.
? Proficiency in verbal and written English. |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| New Product Manufacturing Engineer |
| Position requires
? BS/MS in Electrical/Electronic Engineering
? 3+ years Experience in the design or manufacturing engineering of RF and Microwave (MW) test instrumentation
? 3+ years Experience with New product Introduction (NPI) of RF and Microwave (MW) test instrumentation products
? Experience creating electrical product design or manufacturing test processes and technical documentation of these processes
? Experience with evaluation of new product designs to ensure manufacturability
? Sound knowledge of equipment calibration standards
? Experienced in setting manufacturing product specifications and statistically analyzing product performance
? Sound understanding of instrument measurement uncertainty analysis in accordance to stringent calibration lab requirements eg. ISO17025
? Programming in one or more of the following
o Unix, Linux, RMB, VB, C, C++, VEE, Labview, .NET (dotnet)
? Ability to interact effectively with people at all levels
? Strong knowledge of test instrument application & usage will be an added advantage
? Knowledge or experience in project management will be an added advantage |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Associate Engineer, R&D |
| List minimum education, training and experience needed to perform this job:
1. BSEE/BSET or 3 or more years of related experience.
2. Proficient in RF circuits a plus.
3. Knowledge of Network Analyzer, Signal Generator, Oscilloscopes, etc?
4. Experience with vacuum and cryogenic equipment a plus.
5. Proficient in Excel, MS Word and knowledge of Unix/Linux.
6. Domestic/ International travel; valid passport required. |
| Agilent Technologies, Inc. US |
Boulder |
CO |
9/4/2010
|
| North American Pharmaceutical API Sales |
| ? BS/MS in Chemistry or a Life Sciences discipline, or equivalent.
? 5+ years related direct sales experience selling Life Sciences products/services
? A demonstrated track record of successfully selling against a quota.
? High level of experience interacting with senior level customers from biopharma companies.
? Knowledge of drug development and CMC processes
? Working knowledge of competitive products (services, value propositions, price points).
? Demonstrated commercial selling skills. Strong business development and sales closing skills
? Effective interpersonal communication and telephone sales skills.
? Knowledge of DNA/RNA manufacturing and analysis technology highly desired
? Must be able to travel up to 50% of the time. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientific Associate II |
| Minimum Education Requirements:
Bachelor?s degree in science or engineering field. Internship or undergraduate research project involving analytical laboratory work strongly preferred.
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 |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Formulation Development Scientist |
| - A degree in pharmaceutical sciences, chemistry, chemical engineering, materials science or related field
- PhD (or equivalent degree) and 4+ years of productive, relevant work or postdoctoral experience
- M.Sc. (or equivalent degree) and 7+ years of productive, relevant work experience.
- B.Sc. (or equivalent degree) and 10+ years of productive, relevant work experience.
- Proven ability to apply the principles of the basic sciences such as physical and organic chemistry, thermodynamics, and materials science, to formulation and process development, using a rational, scientific approach.
- Demonstrated ability to develop solutions to complex problems with creativity and innovation
- Formulation development experience on solid oral dosage forms is preferred, especially experience with small molecule NCEs and poorly soluble compounds
- Experience with a range of dosage forms, including liquids, solids and oral, iv formulations, controlled release and pediatric applications would be advantageous
- Expertise in process scale-up and optimization from laboratory scale to pilot scale and registration scale as well as familiarity with engineering scale-up principles, i.e., dimensional analysis.
- Experience applying statistical approaches in the design and analysis of experiments would be advantageous
- Experience working with and managing interactions with contract manufacturing vendors
- Inventive and innovative, self-starter who is comfortable and successful working in a multi-disciplinary team under defined timelines
- Proven teamwork, leadership and collaboration skills, with a demonstrated ability to interact and influence manage all levels of business
- Excellent verbal and written communication skills
- Demonstrated strategic planning, and organizational skills
- Supervisory experience would be a plus but not necessary
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 |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Formulation Development Scientist II |
| A PhD or MS degree (educational concentrations in chemistry, pharmaceutics or engineering preferred)
?Pharmaceutical industry experience of 2-5 years for PhD and 5+ years for MS
?Experience working with small molecule new chemical entities (NCEs) and exposure to early phase formulation development activities
?Experience with a range of dosage forms, including liquids, solids and oral. Experience with IV formulations as well as formulation development for poorly soluble compounds would be advantageous
?Proven experience managing the scale-up and manufacturing of solid oral dosage forms
?Proven ability to apply the principles of the basic sciences, such as physical and organic chemistry, thermodynamics, and materials science, to preformulation and formulation development, using a rational, scientific approach.
?Experience applying statistical approaches in the design and analysis of experiments would be advantageous
?A history of success working in environments defined by innovation and initiative
?Ability to work effectively and comfortably in a multi-disciplinary team under defined timelines
?Excellent leadership, teamwork and organizational skills
?Solid verbal and written communication skills
?Supervisory experience would be a plus but not necessary
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 |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Database Developer/Engineer |
| Desired Skills:
MySQL, Linux, bash,
Nice to have:
Perl, Python, ColdFusion, Java, TalenD, ETL
Experience in working in all phases of the development cycle.
Experience maintaining and developing high availability MySQL RDBMS with replication.
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 |
CA |
9/4/2010
|
| Sr. Auto & Controls Engineer |
| ? Requires a Bachelors degree in an engineering or related discipline. Equivalent experience may be accepted.
? Requires a minimum of 8 years industry work experience.
? Must be very comfortable with 21 CFR Part 11 and GAMP.
? Must have 5 years experience in a GMP pharmaceutical manufacturing environment or other regulated environment.
? Experience with computer-assisted engineering and design software, CAD and graphics skills are a plus.
? Batch processing and/or filling/packaging controls experience are a must.
? BMS experience is a plus.
? Must possess sound technical judgment and use structured decision-making techniques.
? Good oral and written communication skills are a must.
? Strong computer skills are required.
? Must have an ability to provide technical engineering support in a collaborative, team-oriented project environment.
? Strong project management skills are required.
? Project management skills are a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| siRNA Chemistry Associate Scientist (BS/MS) |
| ? BS or MS degree in chemistry
? 5+ years of experience in medicinal or
synthetic chemistry
? Is a creative, flexible, open minded, and
curiosity-driven scientist
? Has the ability to work effectively both
independently and with a multidisciplinary
team of medicinal chemists, biologists,
pharmacologists, engineers, and external
collaborators
? Flexibility to work in a fast-paced,
dynamic environment
? Has excellent oral / written
communication and presentation skills |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior Business Analyst, Bioinformatics |
| Qualifications:
? Idea candidate should have an advanced degree in biology and/or B.S in Computer Science
? At least 3-5 years experience in a scientific or biotech environment
? Strong communications and interpersonal skills
? Proven capabilities interacting with scientists and being customer service oriented
? Ability to work independently and/or as part of a team
? Extensive knowledge in the biology, working experience related to the drug metabolism and pharmacokinetics research process will be strong plus
? Good understanding and practical experience in data management and data analysis tools to support research process
? Solid understanding of relational databases and familiarity with Oracle and/or SQL server
? Strong software engineer knowledge and extensive practical experience |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientist, Translational Safety Biomarker Lab |
| Educational requirements:
BS/MS degree in Biochemistry or Molecular
and/or Cell Biology, Biomedical engineering,
or related fields.
Experience:
5 or more years of practical experience in
assay, reagent, and technology development
in the life sciences industry. The successful
candidate will have experience in molecular
and/or chemical approaches to affinity-
reagent generation. It would be beneficial to
have experience working with biomarker
development, exposure to in vivo studies
both preclinical and/or clinical. The
preferred candidate will have expertise in
data summarization and analysis, oral and
written communication skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Safety Toxicologist |
| ? BS or MSc degree and major in physiology, pharmacology, biomedical engineering or related field.
? Prefer 5 ? 10 years experience in cardiovascular physiology and/or pharmacology research.
? Prefer minimum of 2 years experiences in cardiovascular safety pharmacology research.
? Experience in setting up, conducting and reporting of telemetry studies in dog and monkey.
? Familiar with EMKA jacket system or other external jacket telemetry system and have experience in EMKA ECGAuto computer software (or similar computer software) to analyze cardiovascular telemetry data.
? Experience in using Excel and SAS macro to analyze and report cardiovascular parameters in telemetry.
? Experience in ECG analyses including ECG interval measurements and waveform abnormalities screening in dog and monkey. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Associate, Molecular Imaging, PET/SPECT/CT |
| The ideal candidate will have a BS/MS in Biology, Biochemistry, Animal Sciences, Bioengineering, Biophysics or related field, and 3+ years of hands-on experience with PET/SPECT/CT imaging is a requirement, ideally in a drug discovery environment. Good organizational, interpersonal skills, and excellent communication and presentation skills are desirable.
Skills required: Technical proficiency in all aspects related to PET and extensive hands-on experience with small animal handling (including tail vein injection, catheter placement, perfusion, microdissection), and in vivo pharmacology. Strong computer/computational skills in data analysis. Creativity and the ability to work independently. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| R&D Quality Engineer |
| Education Requirements:
Bachelor of Science degree in Reliability, Quality, Mechanical, Electrical Engineering, Math, Physics or equivalent.
Experience Requirements:
Minimum 5 to 10 years experience in Reliability engineering and testing. Medical Device experience preferred.
Ability to interpret, analyze, and present technical information using practical judgement.
Capable of functioning effectively in a team environment.
Proficient in Excel pivot tables and charting.
Excellent written and oral communication skills.
Demonstrated problem solving skills.
Ability to organize and manage concurrent activities.
Knowledge of advanced data gathering and analysis techniques, including statistical analysis.
Knowledge of standard quality and reliability tools such as FMEA (Failure Modes Effect Analysis), Root Cause Analysis, DOE and Statistics.
Proven ability to communicate effectively and manage relationships at all levels of the organization as well as cross-functionally to achieve reliability goal.
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 |
GA |
9/4/2010
|
| R&D Quality Engineer |
| Education Requirements:
Bachelor of Science degree in Reliability, Quality, Mechanical, Electrical Engineering, Math, Physics or equivalent.
Experience Requirements:
Minimum 5 to 10 years experience in Reliability engineering and testing. Medical Device experience preferred.
Ability to interpret, analyze, and present technical information using practical judgement.
Capable of functioning effectively in a team environment.
Proficient in Excel pivot tables and charting.
Excellent written and oral communication skills.
Demonstrated problem solving skills.
Ability to organize and manage concurrent activities.
Knowledge of advanced data gathering and analysis techniques, including statistical analysis.
Knowledge of standard quality and reliability tools such as FMEA (Failure Modes Effect Analysis), Root Cause Analysis, DOE and Statistics.
Proven ability to communicate effectively and manage relationships at all levels of the organization as well as cross-functionally to achieve reliability goal.
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 |
CA |
9/4/2010
|
| Mfg Process Engineer - Vacaville, Calif |
| BS in Chemical, Biochemical, or Mechanical Engineering, preference in Chemical/Biochemical Engineering.
Written and spoken English
Up to 5 years in a commercial manufacturing environment |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Manager Engineering Systems |
| BS/MS in Engineering (Biomedical/ Bioengineering, Mechanical, Electronic, Chemical, Systems) with minimum of 7 years experience in Life sciences or medical device development.
In-vitro molecular diagnostics experience essential. Familiar with regulatory and compliance requirements for diagnostic tests. Experience in engineering design, optics, hardware, system architecture, application support, and disposables. Minimum 2 years in role as systems engineer or system analyst. Experience working on multi-disciplinary projects. Strong knowledge of assay chemistry for diagnostic tests/molecular biology. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Knowledge Engineering/Text Mining Expert |
| Qualifications:
? Higher education, such as an advanced degree in a business discipline related to life sciences (e.g. biology, bio-informatics, genetics). In-depth knowledge of automated information extraction and/or text mining techniques, computational linguistic analysis and their application to scientific textual data, computational lexicons.
? Concrete experience of problems associated with biomedical and pharmaceutical terminology and data
? Web-oriented technologies and programming languages (Java, Perl, XML, HTML, JavaScript, CGI, etc.)
? 5 years of Knowledge Engineering or Text Mining working experience.
? Recognized Knowledge Engineering/Text Mining Expert.
? Understand the business environment of the business areas to be supported within and outside of NIBR. The business environment includes knowledge of business strategy, objectives, capabilities, processes, data, information, roles fulfilled during drug development, and organizational structures, understanding of influences external to a business organization, such as competitors, regulatory requirements, best in class practices and economic factors.
Reporting
The candidate will be part of the Text Mining Services Group, one of the IS (information services) groups in NITAS and will report to the Head of Text Mining Services located in Basel. The role is based in Cambridge, Massachusetts. The candidate will be member of the team of Knowledge Engineers. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| IS Business Process Analysis Site Lead, (Account Management) |
| -BSc in scientific or IT-related discipline; advanced degree preferred
-Proven senior stakeholder relationship management skills in a complex, geographically distributed organization
-Experience and knowledge in document, information lifecycle, knowledge and records management systems
-Strong operational (managing projects/services) and vendor & supplier management skills
-Evidence of business systems strategy development & execution
-Excellent people, leadership, analytical, written/verbal/presentation communication skills
-Experience with agile software development methodology
-Minimum 3 years management experience in an IT role of similar size & complexity; 7-10 years total experience
-Experience in life sciences industry desirable |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Director Regulatory Affairs |
| Advanced degree in life-sciences, engineering or public health.
1. Greater than 7 years work related profession experience in diagnostic regulatory affairs
2. 3+ years experience in drug/diagnostic regulatory affairs.
3. 5+ years multi/cross functional leadership experience in clinical development, preferably in molecular diagnostics
4. Knowledge of drug development and regulation affairs requirements
5. Familiar with regulatory issues and challenges associated with Drug/Diagnostic co-development and companion diagnostics.
6. Have a track record in successful FDA and ROW premarket submissions and registrations
7. Solid understanding of molecular technologies and the impact on outcomes and diagnostic results
8. Leadership capabilities working across varied cultures, expertise and backgrounds
9. Excellent negotiation skills with regulatory staff on various levels of hierarchy
10. Outstanding interpersonal and communication skills for bridging scientific and business participants, for negotiating timelines and for effective international collaboration. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Dir IT Program Manager |
| Masters degree in computer science or related discipline, at least ten, typically twelve or more years of solid, diverse work experience in IT, or an equivalent combination of education and work experience. 8+ years of pharmaceutical industry especially within R&D, and 6-8 years of experience in drug regulatory publishing and document management. Experienced program manager of large scale multi-year program with estimated team size 75+ associates (IT, business, externals), and program budget approximately 50-75M USD.
? Strong problem solving capabilities: ability to define approach to any type of problem in a pro-active way
? Leadership skills:
o ability to lead a ?virtual? team in a matrix organization and to interact at management and operational level,
o credibility in both business and IT
o address significant business challenges
? Financial skills: business case follow up and financial reporting
? Experienced working in matrix, multi-disciplinary organization driving significant change and business process transformation and working with many stakeholders on all levels (Pharma Global, Development, Corporate); business consultancy engagements a plus
? Previous background/experience in program management ? at least 10 years ? with track record of results (on time, on budget, on customer satisfaction)
? Experienced with management of project teams globally situated
? Strong knowledge of document and submission management business processes and document standards for regulatory submissions particular to the FDA or other Health Authority new drug product applications.
? Excellent Presentation & communication skills: executive board level
? Strong organization and negotiation skills
? Must have a broad industry knowledge, preferably in Health Care/Pharmaceuticals
? Must have excellent understanding of IT and Computer System Validation in a regulated industry
?Previous experience working on Documentum projects is a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Developmental and Molecular Pathways Assay Development Scientist |
| The candidate should have a B.S. or M.S. degree or equivalent in biochemistry, cell biology, engineering or similar with 3+ years of industrial or academic research. Must be highly collaborative, self-motivated, results focused, team-oriented, and have excellent communication and computer skills. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Bioinformatics, Business Analyst (Translational Sciences/ETL Tools) |
| ?Bachelor's degree in computer science and/or advanced degree in biology
?At least 3-5 years experience in application development in a drug discovery, scientific or biotech environment
?Basic understanding of regulatory requirements/compliance policies (e.g. GLP)
?Strong communications and interpersonal skills
?Solid understanding of ETL tools
?Proven capabilities interacting with scientists and being customer service oriented
?Ability to work independently and/or as part of a team
?Knowledge in biology, biological research processes, and applications
?Good understanding and practical experience in fundamentals of software engineering
?Solid understanding of relational databases and familiarity with Oracle and/or SQL server |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Bioinformatician/Translational Sciences (CONTRACT) |
| The successful candidate will have a Ph.D. in bioinformatics, engineering, physics, statistics, applied mathematics, or a related field with a strong computational background. The successful candidate will have experience (2+ years) analyzing genome-scale data sets and a working knowledge of molecular biology. Fluency in at least one statistical package (R/Bioconductor preferred) and one programming or scripting language (e.g. Perl, Ruby, Java, Python) is a must. Experience in Linux environments and clusters is also required. Familiarity with software packages such as Bowtie, Partek, Bfast, GATK, Velvet, Galaxy, IGV, Partek, and Matlad is also required. The successful candidate will be a team player with good communications skills, capable of discussing complex computational concepts with scientists from a variety of backgrounds. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Drexel Co-Op - Maintenance Engineering |
| Minimum Requirements · Engineering major. (Mechanical, Architectural or Electrical) · Completion of the first year of study is required. · Proficiency with Microsoft Windows Word, Excel and familiarity with Project. Skills and Competencies · The intern must have good interpersonal skills to work with design, construction, operational and maintenance personnel. The intern will also be required to interact with tenants. · An understanding of basic engineering concepts. |
| GE Healthcare |
na |
CA |
9/3/2010
|
| Product Specialist ? Filtration and Single-Use |
|
* This is a home office based sales position and as such the candidate must reside within their territory in order to support this role.
* Bachelor?s degree in chemical engineering or mechanical engineering.
* 3+ years of hands-on experience with BioProcess filtration and/or fluid-handling technologies
* Excellent oral presentation and technical writing skills.
* Overnight travel, up to 50%, is required.
To the extent that you are applying for a position that requires you to operate a GE owned/leased, privately owned/leased or rental vehicle for company business, you must have a valid drivers license and be willing to submit to a check of your driving records.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Working knowledge of UNICORN
* Hands-on experience in process development for sizing and optimizing filtration processes
* Strong background in the use of single-use products for normal-flow filtration, cross-flow filtration and fluid handling.
* Technical sales or sales support experience or direct employment in a biotech or pharmaceutical production or process development environment.
* This position requires a high degree of self-motivation and prioritization skills. The candidate must also have a talent for getting along with and working productively with a variety of highly motivated sales personalities.
|
| GE Healthcare |
Westborough |
MA |
9/3/2010
|
| Project Leader, Black Belt |
|
Education/Knowledge:
* Degree in Mechanical engineering, plastics engineering, or a related field
* BS with a min of 10 years relevant industry experience or MS with a min. of 6 years of relevant industry experience
* Strong analytical and quantitative statistical skills; facility with Six Sigma concepts and tools
* Working understanding of regulatory issues related to Biopharmaceutical manufacturing and licensure related to medical devices
Skills:
* Negotiation, communication, presentation and listening skills
* Fluency in written and spoken English
Standard Microsoft Office packages and statistical software
Basic project management
Experience:
Work in a regulated environment (e.g., GMP or ISO quality system)
Other:
Authorization to work in the USA
Ability to travel domestically and internationally on an occasional basis
Ability to perform physical tasks that require mobility, manual dexterity, and visual acuity
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Change agent with strong credibility and influence in the organization
* Masters degree in business related field
* Demonstrated ability to motivate others and achieve results
* Demonstrated commitment for process improvement and product quality
* Customer-focused in defining quality and establishing priorities
Strong oral and written communication skills
Strong interpersonal and leadership skills
Executive level presentation skills
|
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Sr. Scientist/Scientist, Cell Culture Process Development - Agensys, Santa Monica, CA |
| ? Ph.D. in a scientific discipline (Chemical Engineering, Biochemical Engineering or biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of cell culture processes is a necessity. Direct experience with mammalian cell culture process development and process transfer for clinical or commercial manufacturing of biopharmaceutical product(s) highly preferred.? Knowledge in the use of DOE to conduct experiments? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation,centrifugation, clarification, and filtration.? Process validation and cGMP experience is desirable.? Supervisory experience preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Scientist, Process Development in Antibody Drug Conjugates - Agensys, Santa Monica, CA |
| ? Ph.D. in a scientific discipline (Chemistry, Chemical Engineering, and Biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of organic synthesis processes. ? Direct experience in protein purification, conjugation of monoclonal antibodies to small molecules, and process scale-up. ? Experience with HPLC, LC/MS-ESI, chromatographic techniques and immunologic assays including ELISA and immunoblotting? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation, chromatography, UF/DF, and filtration? Supervisory experience and experience with coordinating activities with CMOs are preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Director / Senior Director, Discovery - Agensys, Santa Monica, CA |
| ? Advanced degree (Ph.D., or equivalent) with at least 10 years? experience in an industry setting in Drug Discovery and related areas with an emphasis on target discovery and validation, and monoclonal antibody discovery and engineering. ? Strong background in Oncology drug discovery, evidenced by involvement in development of product candidates from initiation to clinical stage, some experience with biologics is preferred.? Demonstrated record in driving scientific and technical innovations, as evidenced by first or senior authored publications in top-tiered journals.? Demonstrated successful program leadership and multi-project coordination. ? At least 5 years of management experience of multiple groups. ? Proven track record in leading programs to achieve goals and timelines.? Ability to perform successfully in a cross-functional team environment.? Excellent written and verbal communication skills. |
| Astellas Pharma, Inc. |
Oklahoma City |
OK |
9/3/2010
|
| Manager, Engineering |
| ? BS in chemical or mechanical engineering or equivalent relevant pharmaceutical science field required. Advanced degree preferred.? A minimum of 5 ? 8 years experience in solid dosage pharmaceutical manufacturing including packaging required.? A minimum two years management of engineers experience required.. ? Additional knowledge in at least one of the following areas is beneficial: Statistical Inference, SPC, Process Capability, DOE, Sampling plan or Risk Assessment.? Must be able to read, write and understand the English language (statement common to all Job Descriptions) ? Must be able to work to meet deadlines, and utilize problem solving skills. Must be able to gather and evaluate complex data to make effective decisions to accomplish work. Strong communication, prioritization and organizational skills. Attention to detail required. Ability to work independently and as a team member. Accurate record keeping.? Minimum supervision required |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| CMO Manager |
Education/Experience Qualified candidates must have a Master's degree in biology, microbiology, biochemistry, or chemical engineering with a minimum of 5 years experience, or a Bachelor's degree with a minimum of 8 years experience of hands on clinical and/or commercial industry experience in the manufacturing science of biologics (mAbs) and/or cell based therapeutics. Interaction with contract manufacturing organizations and biotech product companies is required and technology transfer and process scale-up are a plus. The skills needed for this position are adequate knowledge of cGMPs, regulatory requirements, and CMC operations in a biotech company; and excellent negotiation and communication skills. |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Assembly Technician I, Repair Center |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| BDM PS US Purchasing Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Biological Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Director of Manufacturing - Process Development |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Director R&D - Electrical and Software Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Director R&D - Systems Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Director, Global Medical Affairs, Advanced Treatment Technologies |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Director, R&D, WW Self Administration of Injectable Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Electrical Controls Technician I B/D Shift |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Instrument Assembly Associate III |
| See above |
| BD (Becton, Dickinson and Company) |
San Francisco |
CA |
9/3/2010
|
| Instrument Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| IT Programmer / Business Analyst - 1st shift |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Lead Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Manager R&D - Mechanical Engineering and Design |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Manager R&D - Software Development |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Manager Software Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Manager, Corporate Safety and Industrial Hygiene |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Manager, R&D |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Manager, R&D |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Manufacturing Director - Plastics/SAIS |
| See above |
| BD (Becton, Dickinson and Company) |
Canaan |
CT |
9/3/2010
|
| Manufacturing Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Manufacturing Integrator, Process Development |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Medical Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Molding Process Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Molding Technology Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Phone Support Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Plastics Molding Engineer - Injection Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Plastics Molding Engineer - Injection Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer Technical Lead |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer, Mechanical/Environmental |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer- Pen Injection Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Principal Polymer Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Process and Automation Development Engineer-PosiFlush |
| See above |
| BD (Becton, Dickinson and Company) |
Madison |
WI |
9/3/2010
|
| Process Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Product Manager - Software |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Production Operator II |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Project Engineer R&D |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Project Manager/System Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Project Statistician |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Quality Management Principal Engineer - Instruments |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| R&D Director, Preanalytical Diagnostics |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Senior Engineer - Process/Project |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Senior Engineer- Electrical/Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Senior Molding Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Senior Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
9/3/2010
|
| Senior Regulatory Compliance Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Senior Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Set Up - D Shift |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sr Systems Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Sr. NetWeaver Administrator |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sr. Optics/Laser Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Sr. Product Engineer (PVA Platform) |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Staff Engineer - Core Team Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Staff Engineer Core Team Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Staff Engineer or Scientist - Chemical Engineering and Biocompatibility |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Staff Engineer or Scientist - Optical Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Systems Validation Specialist II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Systems Validation Specialist II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Systems Validation Specialist II |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Validation Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Validation Engineer (Computer) |
| See above |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Senior SharePoint Engineer |
|
| HireLifeScience.com |
Somerset |
NJ |
9/4/2010
|
| The HireLifeScience.com Career Fair - 9/21/10 |
| Required qualifications to attend:
Candidates must possess a 4 year life science related degree and 2 years professional experience working for a Life Science related company. You may pre-register at http://career.hirelifescience.com/ An invitation to attend will be sent if the minimum qualifications are met. |
| openQ |
Charlottesville |
VA |
9/3/2010
|
| Data Services Project Manager |
| Skills:
• Understanding of, and comfort with, reading medical literature and performing information searches on medically-related topics
• Solid understanding and experience with spreadsheet programs
• Excellent verbal and written communication skills
• Strong analytical skills and technical understanding of data acquisition, data structuring and data quality control
• Prior experience interfacing with customers about data-related projects
• Strong team player and the proven ability to work independently
Education:
• Minimum of Masters level degree in life sciences field (PhD preferred) and at least 3 years relevant experience in a life sciences-driven data company.
|
