For more detailed program information and to apply please visit our website at: http://www.nycteachingfellows.org. ]]> 2009-11-02T14:50:14-05:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1448336563.html text 2009-11-02T14:50:14-05:00 http://philadelphia.craigslist.org/sci/1447294006.html

Article One Partners (www.articleonepartners.com) lists requests for articles, patents, research papers, product literature or any written information from anywhere in the world that describes particular technologies as of a historic date. Article One’s research projects are called Patent Studies.


There are over 20 studies listed for some of the most important technologies worldwide, such as pharmaceuticals (Lunesta, Levitra, Geodon etc.), telephone apparati (Speech Processing by RIMM), software (Twitter.com), wireless technology, and Blu-ray disc drives on the Playstation 3.


Article One Partners needs you to find documented information-- prior art. By searching for prior art, you gain the invaluable experience of researching scientific documents, earn profit-sharing points, and may earn up to $50,000 per study. More than twenty studies are currently offered for over $1,000,000 in compensation rewards. Rewards are distributed when Article One determines that the public written information you submit can show a patent to be invalid.


Begin work immediately, register at www.articleonepartners.com, browse the Studies (check your eligibility), and apply your knowledge, research and network to find Prior Art. Article One will review your submissions and tell you if you have earned the cash rewards. Your active participation in Article One will earn profit sharing points. (The profit-sharing plan is described in detail on our website.)


By joining and participating in the community, you earn profit-sharing points. To learn more, come visit us at articleonepartners.com and register for free as an advisor. Also, Article One Partners will soon be adding new studies soon, so by registering now, advisors can get a head start on submitting new prior art.


Article One Partners is a web-based patent research company that searches for prior art. Prior art refers to the entire body of publicly available information that can potentially invalidate a patent by showing that its ideas were known by the date of invention of the patent. Invalidating prior art shows that an invention described in the claims of a patent existed before a date of invention. Prior art can also be used to establish the strength of a patent.


The Studies list patents with a description of the technology and the historic date. Patents are granted because the U.S. Patent Office concludes that the description of the technology in the patent is the first in the world. But the Patent Office is limited in being able to research worldwide public information. Article One offers a citizen’s review to check whether the patent description is the first. If you show an earlier description, you can earn $50k and high profile press as a state of the art researcher for recognition in industry and career building.


The public written information is called Prior Art. The historic date by which the Prior Art must be dated is called “Latest Date for Prior Art.” Each Study links to a patent or patents, and provides a written description of the technology and the latest date for Prior Art.


- Reduce the monopoly pricing you pay for products covered by patents which should not have been granted, help to reform U.S. patent law – and get compensated for your efforts and the value of your knowledge!


****When you register at AOP, please use the registration code Craig.****]]> 2009-11-01T19:52:14-05:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1447294006.html text 2009-11-01T19:52:14-05:00 http://philadelphia.craigslist.org/sci/1442920072.html Position and Qualifications:

Amnis Corporation is looking for a field service engineer to support installations at customer sites for its ImageStream flow-based, high throughput, multi-spectral cell imaging instruments. The ImageStream product line is used by pharmaceutical and biotech companies as well as government and academic labs for cell-based research. The company is expanding its Customer Service operations and is currently looking for a skilled service engineer on the east coast of the United States.

This position requires a high level of proficiency with complex opto/electro/mechanical and fluidic systems. The individual must be well versed in operating, trouble-shooting and rectifying problems with complex instrumentation. Experience with flow cytometry, cell analysis instrumentation, biological samples, processing systems, reagents and protocols is very desirable. Outstanding interpersonal skills are essential. This position will involve travel, significant contact with customers. and necessitate the ability to maintain a calm and professional demeanor at all times. This individual must be well versed in translating and communicating customer needs to all facets of the Amnis organization including Research and Development, Applications Development, Production and Sales. A track record of at least five years, demonstrating a positive attitude and ability to work with customers to understand their needs to fix problems in an efficient manner, is required.

Send resumes to boster@amnis.com. Insert “Field Service Engineer: East Coast (your name)” in the SUBJECT line of the email.
Or send resume to:
HR Department
Attn: Field Service Manager
Amnis Corporation
2505 Third Avenue, Suite 210
Seattle, WA 98121
Or Fax your resume to: (206) 576-6895
]]> 2009-10-29T13:01:16-04:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1442920072.html text 2009-10-29T13:01:16-04:00 http://philadelphia.craigslist.org/sci/1442634071.html http://apply.dscience.com/videoanalyst]]> 2009-10-29T10:06:26-04:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1442634071.html text 2009-10-29T10:06:26-04:00 http://philadelphia.craigslist.org/sci/1441688924.html 2009-10-28T15:20:02-04:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1441688924.html text 2009-10-28T15:20:02-04:00 http://philadelphia.craigslist.org/sci/1441385922.html




WHAT WE OFFER

Team-based and scientifically exciting environment

Easily accessible by train and highway

Medical and dental insurance

Flexible Spending Accounts, health and dependent care

Short- and long-term disability insurance

401(k) plan with immediate vesting of employer contribution

24 days off plus 7 holidays; time off is immediately available

Company-provided laptop; you may occasionally telecommute





JOB DUTIES

Work with pharmaceutical clients, authors, and key opinion leaders

Write/edit medical communications and publications including manuscripts, posters, slide kits, and product monographs

Work with an account manager to coordinate activities with client and internal teams

Help implement publication planning strategy and implementation

Ensure your writing/editing is medically and scientifically accurate and meets client objectives, timelines and budgets

Develop and edit content at direction/guidance of authors

Assist with reference gathering and literature searches

Combine review comments into subsequent revisions

Circulate drafts for further review/finalization





REQUIREMENTS/MUST HAVES

PhD in biology, pharmacology, biochemistry, biomedicine, bioengineering or medically related field (MD or PharmD)

Medical writing experience directed to scientists and physicians

Experience working with pharmaceutical clients, thought leaders, and authors

Superlative communications skills

Excellent project management skills

Familiarity with writing and publication guidelines, journal requirements, and other publications¡¦ standards

Knowledge of American Medical Association (AMA) guidelines and Good Publication Practice (GPP) for pharmaceutical companies





HOW TO APPLY

To apply, please send your curriculum vitae and cover letter to: cynthia.kabbe@ubc-envisiongroup.com. For further information, please visit our website at www.envisionpharma.com.









]]> 2009-10-28T12:35:33-04:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1441385922.html text 2009-10-28T12:35:33-04:00 http://philadelphia.craigslist.org/sci/1441221831.html

Location Ft. Lauderdale, FL
Department Technical Ops
Job Description Under general direction, directs and oversees all aspects of manufacturing operations; ensures that all phases of manufacturing activities are performed in a safe manner and in compliance with cGMP and SOP's; and ensures that Company and government policies and procedures are adhered to involving all aspects of the job including EHS, Fianance and Human Resources responsibilities. Applies lean Six sigma practices.Reports to the site General Manager and is accountable for meeting the goals and objectives of the Manufacturing Operations Management team.

• Carries out managerial responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws.
• Assures a timely and efficient flow of manufactured products.
• Assists Director of Manufacturing with department structure, development of manufacturing budget and long range plans to meet the required production levels of the manufacturing area; controls and manages the operating budget.
• Conducts performance evaluations for exempt direct reports; assists supervisors with subordinate performance evaluation process for their areas; applies effective implementation of employee disciplinary corrective action programs.
• Reviews procedures on an on-going basis seeking ways to improve the efficiency of manufacturing operations; ensures compliance with all company equipment and safety rules and regulations.
• Evaluates existing and recommends new equipment, which will enhance/improve the manufacturing process.
• Executes process validations of new and existing products following written protocols.
• Ensures that the implementation and documentation of manufacturing SOP and safety training are performed properly and on a timely basis.
• Ensures that SOP’s are reviewed and updated as needed; and that all manufacturing processes are performed in compliance with cGMP, SOP, and OSHA requirements.
• Interfaces with scheduling personnel to meet product forecast requirements and to trouble-shoot capacity constraints; works closely with subordinate supervisors to ensure that department meets scheduled forecasts and manufacturing plans.
• Supports and works closely with Technical Services Department for process definition scale up and transfer.
• Keeps Director of Manufacturing apprised of all current manufacturing process issues; troubleshoots and resolves production and equipment problems.
• Creates and maintains a working environment that stimulates innovative ideas and change, and manages implementation of the same in a timely manner; maintains management presence in the manufacturing area through the monitoring and control of manufacturing process.
• Assures the timely and thorough completion of processing paperwork and MRP entries.
• Control departmental spending based on approved annual expense budget.
• May meet monthly/annual plan attainment to assure customer service is satisfied.
• Performs related duties as assigned.
"Immediate opportunities available on second and third shift. The position requires the flexibility to work first, second or third shifts according to the demands of the business."


This position is to cover 2nd and/or 3rd shift.
Qualifications Required Knowledge and Skills:
Knowledge of:
• Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), DEA, and other regulatory requirements.
• Manufacturing processes, equipment procedures and systems.
• Principals of safety, workers’ compensation, OSHA, and related principals/practices.
• Principals of mathematical and statistical computations.
• Current Company policies and procedures, including safety rules and regulations.
• Pharmaceutical principals, practices, and their application.
• Principals and practices of budget preparation and administration.
• Proper English, grammar, spelling, and punctuation.
• Basic computer programs and applications.

Skill in:
• Implementing goals, objectives and practices for effective, efficient and cost effective management of allocated resources.
• Communicating clearly and concisely, both orally and in writing.
• Effectively speaking and presenting professional training sessions, one-on-one or with a group of employees.
• Analyzing and trouble-shooting problems, identifying solutions, recommending and implementing methods, procedures and/or techniques for resolution.
• Establishing and maintaining cooperative working relationships with individuals contacted in the course of work.
• Responding to common inquiries, complaints, conflict/resolution situations from subordinates or other employees in the work area.
• Selecting, training, supervising, and evaluating department subordinates.
• Functioning as a team leader, coach and mentor, and managing, directing, and coordinating the work of professional, technical and clerical personnel.
• Allocating limited resources in a cost saving, efficient manner.
• Handling multiple projects, duties and assignments.

Physical Requirements and Working Conditions: Incumbents in this class are subject to regular and/or routine periods of sitting, standing, walking and visual acuity to monitor. Work is performed in office and manufacturing environments. Exposure to noise levels will vary from moderate to loud depending upon production machinery usage.


Education
Minimum Qualifications: Bachelor's degree from an accredited college or university, and five (5) – seven (7) years experience or an equivalent combination of education and experience in addition to four (4) or more years of progressively more responsible manufacturing management experience, preferably in pharmaceutical, food, or cosmetic industry.]]> 2009-10-28T11:02:36-04:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1441221831.html text 2009-10-28T11:02:36-04:00 http://philadelphia.craigslist.org/sci/1439793227.html
Gamry Instruments is a manufacturer of electrochemical laboratory instruments and software. Founded in 1989, Gamry develops and markets equipment worldwide to end users in various industries including batteries & fuel cells, corrosion prevention, materials, metals, biomaterials, sensors, and paints & coatings, to name a few. Gamry is a small, closely held corporation. ]]> 2009-10-27T11:52:19-04:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1439793227.html text 2009-10-27T11:52:19-04:00 http://philadelphia.craigslist.org/sci/1438369814.html 2009-10-26T13:13:44-04:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1438369814.html text 2009-10-26T13:13:44-04:00 http://philadelphia.craigslist.org/sci/1438069389.html
Qualifications: The ideal candidate will possess experience in research and development of fuel cells and/or batteries. A PhD is required. The candidate will be expected to develop experimental protocols, conduct research, manage data and report results. This position is located in Cheyenne, WY.

Technical Expertise: Candidates should have a strong background in the electrochemical characterization of fuel cells and batteries, including appropriate analysis techniques, such as:

Electrochemical Impedence Spectroscopy
Cyclic Voltammetry
Linear Polarization Techniques
Spectroscopy tools
Project Delivery
Strong chemistry background and intuition

The following are desired but not required:

Experience with Direct Liquid Fuel Cell Technology
Experience with passive fuel system design
Experience with techniques for enhancing catalyst performance

Compensation: DOE
Title: DOE

www.ndcpower.com]]> 2009-10-26T10:37:22-04:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1438069389.html text 2009-10-26T10:37:22-04:00 http://philadelphia.craigslist.org/sci/1437955552.html DEPARTMENT: Chemical Development
REPORTS TO: Senior Radiochemist


Description:

Design and execute synthetic schemes for development and optimization of radio-labeled drug molecules candidates for research and commercial purposes.

Duties include:

• Development of radiosynthetic processes for production of radiolabeled drug molecules
• Optimization and scale up of chemical processes for transfer to manufacturing
• Documentation of chemical processes and controls
• Development, execution and review of batch records
• Maintenance of the chemistry laboratory, corresponding equipments and purchase of equipment and reagents as necessary

Qualifications:

• BS degree or equivalent in chemistry or a related field with preferable 2+ years of experience
• Working knowledge of organic chemistry is highly desirable
• Working knowledge of HPLC and related analytical techniques such as LC/MS, GC, and NMR is highly desirable
• Ability to work independently in a highly focused manner
• Good organizational skills
• Excellent written and verbal communication skills
• Familiarity with radiochemistry desirable but not required
• Ability to travel as needed
]]> 2009-10-26T09:11:25-04:00 en-us Copyright © 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1437955552.html text 2009-10-26T09:11:25-04:00 http://philadelphia.craigslist.org/sci/1434747398.html DEPARTMENT: Chemical Development
REPORTS TO: Senior Radiochemist


Description:

Responsibilities include the manufacture and process development of radioactive drug products for support of clinical and non-clinical studies. Preparation and maintenance of cGMP manufacturing equipment and cGMP production facilities. Execution of manufacturing processes in accordance to applicable regulatory requirements. As necessary support non-clinical radioactive drug product development and manufacturing for preclinical pharmacology studies.


Duties include:

• Production of radiopharmaceuticals for clinical and non-clinical use
• Execution and review of batch records
• Preparation of production reagents and components
• Provide quality control support as needed
• Maintenance and cleaning of production and related equipment
• Compliance to regulatory (USP <823>)
• Write Standard Operating Procedures (SOPs) and technical reports
• Maintain a well-organized data filing system

Qualifications:

• BS degree or equivalent in a scientific field with preferable 2+ years of experience in a cGMP production environment is highly desirable
• Working knowledge of HPLC and other analytical techniques such as LC/MS, GC, and NMR is desirable
• Strong desire to work independently in a highly focused manner
• Good organizational skills
• Excellent written and verbal communication skills
• Experience with pharmaceutical cGMP/GLP, ICH, FDA guidelines desirable but not necessary
• Knowledge of synthetic organic chemistry desirable but not necessary

Located in University City, Philadelphia, team members enjoy competitive pay, benefits package and the opportunity to be part of our revolutionary science. If you are interested in joining our team, we encourage you to provide a cover letter indicating why you are the ideal candidate for this position. Qualified candidates may forward their resume, cover letter and salary requirements to kruzik@avidrp.com. Please, no phone calls. Recruiters, please do not contact this job posting. EOE.


]]> 2009-10-23T16:31:17-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1434747398.html text 2009-10-23T16:31:17-04:00 http://philadelphia.craigslist.org/sci/1434600550.html Requirements
Demonstrated technical proficiency with cell culture and various cell-based bioassays. Outstanding organizational skills. Ability to multi-task, work independently and work in a team environment. Excellent oral and written communication skills. Ability to work in a dynamic fluid environment.

Areas of expertise desired: Cell Biology, Cell Culture, Bioassay Development]]> 2009-10-23T15:08:06-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1434600550.html text 2009-10-23T15:08:06-04:00 http://philadelphia.craigslist.org/sci/1433500019.html United BioSource Corporation (www.unitedbiosource.com) is a global pharmaceutical services company with a strong focus on customized technology solutions that have scientific validity for the drug development and commercialization process. The Company has more than 1,300 employees and 20 offices worldwide. Our company is profitable, rapidly growing, and is the clear leader and innovator in bringing together science and technology solutions for clinical trials. We have a focused mission--to help reduce healthcare costs by making the drug development process more efficient and cost-effective for our clients through the use of technology.

UBC Clinical Technologies—a division of UBC with offices located in downtown San Francisco, Langhorne (Pennsylvania), and London, England—helps life sciences companies by providing highly-customized web-based software including electronic Patient Reported Outcomes (ePRO) and interactive voice and web response systems (IVRS/IWRS) that make the clinical development processes for new medicines and medical devices more efficient and more reliable. With a technology-oriented background, we work hard to maintain a casual, fun and motivated work culture globally.

Because of the success of our technologies we are experiencing rapid growth and currently have a technical IVRS Project Manager position open in the Langhorne, PA, office for candidates who like working in a fast-paced, entrepreneurial environment.

If this position sounds like a perfect fit with your experience and interests—and you want to be part of the excitement of leading technology company in the pharmaceutical industry—then we want to hear from you!

Important Notes:
----------------------------------------------
Send your resume and salary requirements to careers.technologies@unitedbiosource.com, and include the job title & job location in the subject line of your e-mail. We have multiple positions available across the country, and supplying this information will result in your resume being reviewed sooner!

Resumes sent without salary requirements may not be considered.

Although candidates from other locations may be considered, no relocation assistance will be offered for these positions.

Duties & Responsibilities:
----------------------------------------------
Serve as primary point of contact to the external client and to the internal development staff during the development lifecycle of a system.

Track and manage project schedules, status and issues.

Handle customer issues and proactively drive resolution.

Use project management skills to organize and lead client meetings, issue tasks, attend to details, and drive a project through a defined process to completion.

Gather and document all system requirements.

Manage project budgets and scope.

Identify and execute additional product enhancement/customer support opportunities with existing clients.

May be responsible for after-hours & weekend on-call technical support as needed, on a rotation basis.

All responsibilities should be carried out in a professional manner that supports the accomplishment of business objectives and encourages a positive team-oriented work environment.


Required Skills & Experience:
----------------------------------------------
Bachelor's degree plus five years of overall experience in managing team projects with at least 2 years experience in the Pharmaceutical/Biotech industry preferred. Further years of work experience may be considered in lieu of educational requirements.

Experience working in Clinical Trial environment highly desirable.

Strong technical skills including knowledge of software development process.

Superior verbal and written communication and interpersonal skills including the ability to deliver effective training programs and large group presentations including facilitating team processes in person and via telephone or e-mail.

Ability to quickly learn and apply new skills, procedures and approaches.
Demonstrated ability to meet very short deadlines & multi-task in an extremely fast-paced work environment with little direct supervision.

Proven ability to work in a team-oriented environment, providing back-up support to team members & establishing/maintaining effective work relationships with co-workers within and across functional areas.

Ability to apply extreme attention to detail and organization in all aspects of work.

Previously demonstrated proactive and positive approach to tasks and projects overall, as well as to the types of scheduling & process changes that are inherent in a fast-paced business.

Ability and willingness to occasionally travel nationally and internationally. Some travel does take place on/over weekends. ]]> 2009-10-22T19:51:47-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1433500019.html text 2009-10-22T19:51:47-04:00 http://philadelphia.craigslist.org/sci/1431506037.html
We offer excellent benefits and a profit-sharing program that rewards performance and results. Our comprehensive benefits program includes: medical, dental, vision, prescription card, 401k with 50% company match, tuition assistance, bonus plan, and more. REPSG is an equal opportunity/affirmative action employer that strongly values diversity. EOE/AA/M/F/V/D
Requirements
This position requires a B.S. Degree in Geology or similar Environmental discipline.

Strong writing skills required.

Prior experience in environmental consulting preferred.

Candidate must be authorized to work in the United States without requiring the company to sponsor a visa.

Job location is Philadelphia, PA
Compensation
Competitive with excellent benefits
]]> 2009-10-21T14:28:07-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1431506037.html text 2009-10-21T14:28:07-04:00 http://philadelphia.craigslist.org/sci/1431322643.html Integral Molecular is a Biotechnology Company that provides innovative solutions for scientific research and drug discovery applications involving cellular and viral integral membrane proteins. Visit Integral Molecular at http://www.integralmolecular.com/

Job Title: Research Associate (Permanent, Full time)
Job Description:
This position will involve conducting laboratory research and supporting general R&D operations at Integral Molecular. The position will involve both research and production of biomedical research products. You will be working with a dedicated group of scientists on the development and commercialization of biomedical technologies. Projects may involve cell culture, virology, DNA preparation, liquid handling automation, and cell-based assays (western blot, ELISA, immunofluorescence, flow cytometry).

Qualifications:
The position requires a Bachelor's degree in biology, bioengineering, or a related field. 1-2 years of laboratory and cell culture experience is desired. Candidates must have a demonstrated ability to learn quickly and follow protocols, and must be attentive to detail.

Application Instructions:
Please submit your resume and cover letter to careers@integralmolecular.com with Job ID# 090306 in the Subject title]]> 2009-10-21T12:49:56-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1431322643.html text 2009-10-21T12:49:56-04:00 http://philadelphia.craigslist.org/sci/1431231040.html .
ESSENTIAL DUTIES AND RESPONSIBILITIES
Responsibilities will include, but are not limited to, assisting in preparing or updating departmental procedures related to data management , training junior associates in data management procedures and systems, preparing and/or presenting data management related trainings at Investigator’s Meeting, including CRF and completion guideline, coordinating with CRF designer on CRF development and approval, ensuring study quality of document control, Data Management Project Files, and information on the shared drive, updating planning documents or reports in a timely manner, providing quality and timely review on Data Management documents, preparing and updating of clinical data management documents on study level, including but not limited to Data Management Plans, Data Entry Guideline, Edit Check Specifications, Self-Evident Change, note to file, SAE Reconciliation plan and other documents, reviewing and ensuring that the following documents are up to date: medical coding guideline, Data Specification/CRF annotation, external data specification, electronic transfer specification, and quality control documents, coordinating database development, validation programming, merging programs, external data loading or conversion, data access (e.g. I-review) and all associated testing with Data Management team, testing reports, performing pass 2 database testing if dedicated CDA is not available, discrepancy management, overseeing data quality in a timely fashion, ensuring that other routine Data Management activities and deliverables are implemented and maintained including data inflow, medical coding guideline, Data Specification/CRF annotation, external data specification, electronic transfer specification, and quality control documents, coordinating database development, validation programming, merging programs, external data loading or conversion, data access (e.g. I-review) and all associated testing with Data Management team, testing reports, performing pass 2 database testing if dedicated CDA is not available, discrepancy management, overseeing data quality in a timely fashion, ensuring that other routine Data Management activities and deliverables are implemented and maintained including data inflow, medical coding, external data coordination, and conversion/uploading/extraction/access/data transfer, facilitating change management for study related data management activities, e.g, CRF, database, validation programming, labs, merging program, etc, data quality and consistency, responsible for providing responses/corrective actions to audit reports and other quality initiatives, database closure activities for internal databases, including coordination of listing reviews and SAE reconciliation, among other database closure activities, travel to the study sites for query resolution if needed, performing vendor audits for external data sources, ensuring that the SOP of Database Closure is followed for database closure activities, managing deliverables of clinical data management outsourced partners, communicating with other team members, reporting issues, and coordinating team meetings, tracking data management study performance and and providing project tracking reports to routine or ad hoc request, assisting in the contract and budget/expense tracking related to data management on the study level, performing other data management functions as necessary, support departmental initiatives and assisting in other tasks as needed.

TECHNICAL SKILLS REQUIRED
• Bachelor’s degree is required, graduate degree preferred. Nursing, PA, other clinical education or computer science is highly desirable.
• Minimum of 5 years in Data Management
• Clinical Operations experience a plus, strong knowledge of medical terminology and clinical trial process is required.
• Working knowledge of Oracle Clinical database and SAS dataset structure, MedDRA and WHO drug coding dictionaries
• Excellent writing skills
• Must be detail oriented and possess superior organizational and project management skills.
• The incumbent must be computer literate in MS Windows-based applications, possess excellent communication skills, including the ability to speak, write and understand English to comply with written procedures, instructions, SOPs and other documents.

Resume must include salary requirements for consideration
]]> 2009-10-21T12:01:07-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1431231040.html text 2009-10-21T12:01:07-04:00 http://philadelphia.craigslist.org/sci/1431208646.html

WHAT WE OFFER
Team-based and scientifically exciting environment
Easily accessible by train and highway
Medical and dental insurance
Flexible Spending Accounts, health and dependent care
Short- and long-term disability insurance
401(k) plan with immediate vesting of employer contribution
24 days off plus 7 holidays; time off is immediately available
Company-provided laptop; you may occasionally telecommute


JOB DUTIES
Work with pharmaceutical clients, authors, and key opinion leaders
Write/edit medical communications and publications including manuscripts, posters, slide kits, and product monographs
Work with an account manager to coordinate activities with client and internal teams
Help implement publication planning strategy and implementation
Ensure your writing/editing is medically and scientifically accurate and meets client objectives, timelines and budgets
Develop and edit content at direction/guidance of authors
Assist with reference gathering and literature searches
Combine review comments into subsequent revisions
Circulate drafts for further review/finalization


REQUIREMENTS/MUST HAVES
PhD in biology, pharmacology, biochemistry, biomedicine, bioengineering or medically related field (MD or PharmD)
Medical writing experience directed to scientists and physicians
Experience working with pharmaceutical clients, thought leaders, and authors
Superlative communications skills
Excellent project management skills
Familiarity with writing and publication guidelines, journal requirements, and other publications¡¦ standards
Knowledge of American Medical Association (AMA) guidelines and Good Publication Practice (GPP) for pharmaceutical companies


HOW TO APPLY
To apply, please send your curriculum vitae and cover letter to: cynthia.kabbe@ubc-envisiongroup.com. For further information, please visit our website at www.envisionpharma.com.




]]> 2009-10-21T11:48:44-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1431208646.html text 2009-10-21T11:48:44-04:00 http://philadelphia.craigslist.org/sci/1431128898.html
Responsibilities include:
• Providing technical assistance in biological laboratory research in the area of cell-cell signaling;
• Utilizing basic techniques in the following areas:
o Molecular biology, i.e., DNA cloning
o Biochemistry, i.e., protein purification and enzyme assays
o Cell biology, i.e., immunostaining and microscopy
o Genetics, i.e. maintenance and handling of Drosophila stocks
• Assisting in laboratory organization and support, including ordering and making reagents; and
• Other duties as assigned.
Preferred Qualifications:
• Bachelor’s Degree in an appropriate field of science or technology or equivalent in education and experience;
• Two-four years of related research experience, or an advanced degree in an appropriate area of science or technology and one or more years of related laboratory experience;
• Strong organizational and communication skills;
• Highly self motivated and able to work in a diverse laboratory environment; and
• Able to interact well with others and work as part of a team.
Please send your resume, cover letter, and salary requirements to pohld@hhmi.org. We are an equal opportunity employer.

]]> 2009-10-21T11:03:06-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1431128898.html text 2009-10-21T11:03:06-04:00 http://philadelphia.craigslist.org/sci/1429715807.html
A Philadelphia based chemical manufacturing company is seeking an individual to manage all production operations. This is a high profile position reporting to the President/Chief Operating Officer of the company.
Key functions include (are not limited to):

1.Logistics
• Coordinate in-bound and out-bound shipments with Sales dept.
• Maintain inventories of raw materials and finished products at set points.
• Perpetual inventories: monthly, quarterly and annual physical inventories.
2. Production
• Coordinate most cost effective and timely process.
• Ensure the proper resources are used in manufacturing
• Provide process & equipment training of all plant personnel and maintain training records.
3. Personnel
• Optimize man-power usage
• Maintain attendance and demerit schedules for union plant personnel.
4. Maintenance and Engineering
• Oversee all maintenance operations including: Preventive maintenance schedules and records. Work order schedules and records. Maintenance personnel demands and scheduling.
• Provide engineering oversight of all major plant expansion/design projects.
• Maintain facility plant boiler operation.
5. Security
• Manage all security staff. Develop and implement a security operations program.
6. Environmental and Non-environmental Regulatory Compliance
• Monthly sampling and testing. Semi-annual compliance reporting.
• Manage all compliance matters related to PA DEP, EPA, OSHA, Philadelphia L&I, etc.
• Compile and submit TRI, TIER II/III reports.
• Provide all environmental and safety training of facility personnel.
7. Quality Assurance
• Oversee all aspects of QA, including raw material, in-process and finished goods testing. Maintain calibrations of all laboratory and plant personnel.
8. Other duties as may be appropriate for this position.

Experience
The ideal candidate will have a BS Chemical Engineering (MS preferred) and a minimum of 8 years chemical plant management experience. Candidates should also have a strong understanding of reaction chemistry, specifically esterification/condensation chemistry, as well as a strong working knowledge of environmental compliance requirements.

Compensation
Salary will be commensurate with candidate’s qualifications. The company currently offers benefits, including medical, dental, vision, short term disability and life insurance plans as well as a 401K and AFLAC participation.

Please forward your resume to Sandi King @ sandi.king@phila.gov or fax it to (215) 683-2141!
]]> 2009-10-20T12:12:40-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1429715807.html text 2009-10-20T12:12:40-04:00 http://philadelphia.craigslist.org/sci/1429155823.html
SUMMARY
In coordination with the R&D Scientists, perform procedures and analyses required for development of commercial immunoassay kits.

ESSENTIAL DUTIES AND RESPONSIBILITIES
-Proficient in aseptic technique
-Experience working with biological fluids (blood, sera, etc..) and universal precautions
-Familiarity with cGMP guidelines
- Maintaining inventories
- Prepare solutions/reagents following standardized formulas or written protocols
- Complete other related duties and responsibilities as assigned
- ELISA and chemistry experience preferred


QUALIFICATIONS
- Bachelor of Science or Associates degree in Biological Sciences
- Experience in immunoassay development and/or formulation chemistry preferred
- Show strong desire for working in the research lab

]]> 2009-10-19T22:45:52-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1429155823.html text 2009-10-19T22:45:52-04:00 http://philadelphia.craigslist.org/sci/1426619009.html
QualTek is a contract research biomedical laboratory that works with major pharmaceutical and biomedical companies in the areas of oncology, inflammatory diseases and neural and eye disorders. QualTek’s expertise in immunohistochemistry, a method of visualizing and localizing proteins in tissues, has uses in almost all areas of biomedical research from basic R&D, to product inception, and through clinical trials and advanced patient diagnosis of disease. We are at the forefront of the effort assisting our customers in identifying new biomarkers for disease diagnosis, disease detection and treatment.

The candidate should have a minimum of a Masters degree with emphasis in molecular biology, cell biology, and/or pathology. Work experience is a plus but newly degreed candidates will be considered as well. Immunohistochemistry experience is also a plus but we will train the successful candidate in all aspects of immunohistochemistry.

You should be a person who is intelligent, creative, pays attention to detail and can handle more then one task at a time. You should also have good communication skills, a solid scientific knowledge base and be able to write detailed reports in a clear and concise manner. You should also be willing to work to meet deadlines and stay on top of all projects you are responsible for. QualTek is a small company that prides itself on teamwork, thus good interpersonal skills are a must.

Please send your resume with a cover letter. The cover letter is important. We want to see your writing skills and style and understand how you as a candidate can fit in with our growing organization. Salary history and references will be required for the successful candidate.

For more information about QualTek please see our website: http://www.qmlabs.com

]]> 2009-10-18T10:32:23-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1426619009.html text 2009-10-18T10:32:23-04:00 http://philadelphia.craigslist.org/sci/1421021954.html
Are you noted for extraordinary attention to detail? Do you have 100% on-time attendance? Do you have great hand skills with small things like needlepoint or miniature model building? This might indicate you are a candidate for a career in high tech manufacturing at Clear Align.

Clear Align is the fastest growing company in the Mid-Atlantic Region as ranked #1 by Inc Magazine on the Inc. 500 list and #135 in the Nation. The company designs, prototypes and manufactures custom imaging, sensing and fiber optic systems for defense, aerospace and commercial customers. Clear Align’s imaging expertise spans the UV, visible, NIR, SWIR, MWIR, and LWIR portions of the spectrum, delivering both narrow- and wide field-of-view systems. Fiber-optic and sensing expertise includes optical integration for communications, remote sensing and targeting, as well as medical fiber optics.

We can teach you about this market and technology and open up a niche career in a growing market if you are hard-working and willing to take on challenges. No task can be beneath you. You should bring a bubbly positive attitude to work every day and enjoy being part of a fast moving organization. This position will allow the individual to work closely with our laboratory technicians, and the right candidate will have the ideal opportunity to grow into a position in high-tech operations and assembly.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following:
• Ensure the entire facility passes in depth cleanliness audits and is in top condition for tours and visits by our high profile clients including congressman, senators, military officials and defense contractors (3 hrs per day).
• Performing basic laboratory procedures under the supervision and instruction of a supervisor (5 hrs per day).
• You will be expected to learn new skills quickly and be good at visualizing assembly and 3D images.
• You should be interested in learning to work with sensitive equipment and devices.

The candidate should have the following attributes:
• Punctuality and attendance are key to this individual’s success.
• Professional cleaning experience and work with a floor buffer a plus.
• Previous experiences in a high-tech manufacturing environment with detailed hand work a plus.
• Valid drivers license and US Citizenship required.
• Candidates will be tested for proficiency in mathematics, Excel and Microsoft Word.
• *If you don’t have direct experience, please take the time to explain in your cover letter why you would be good for this position and could be trained.*

This is a full time job, but part-time applicants will be considered. Full time employees enjoy medical, dental benefits, life insurance, and a generous vacation policy. Eight hour schedule is flexible, but candidate must be willing to start early or end late to accommodate office/laboratory cleaning outside of working hours. To apply, e-mail your resume to careers@clearalign.com and be sure to put “Job 01209” in the subject line or you will not get considered for the job.

Clear Align is an equal-opportunity employer
Clear Align
www.clearalign.com
2550 Boulevard of the Generals, Suite 280,
Eagleville, PA 19403
484-956-0510
]]> 2009-10-14T11:52:27-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1421021954.html text 2009-10-14T11:52:27-04:00 http://philadelphia.craigslist.org/sci/1420815712.html http://www.ansp.org/research/biodiv/.

Working as a database administrator, the database developer will share responsibility for maintaining the integrity of the databases and will work closely with curatorial and research staff to develop informatics tools for efficient data capture, quality control, visualization and analysis, and web-based data access. This is an ideal position for a programmer that is interested in both biodiversity research, full life-cycle development, and working closely with end users to develop creative database solutions.

Required Skills:
• B.Sc. in Computer Science or equivalent experience
• Interest in biology and biodiversity
• Programming in a LAMP environment (Linux, Apache, MySQL, PHP)
• Database administration using Filemaker and MS Access
• Linux server administration
• HTML/CSS and basic web design
• Good communication skills and ability to work closely with end users

Desired Skills:
• Advanced degree and/or 2-3 years experiences with biodiversity databases
• Training and/or experience in zoology or botany
• Experience with some of the following: a portal engine/CMS like Joomla, a PHP-based application framework like Prado; qmail/ezmlm, ImageMagick, MapServer, DiGIR/TAPIR
• Ability to assist with proposal development

To Apply:
Send resume, statement of interest (including desired salary range) and the names and email addresses of three references to: hrjobs@ansp.org. Job #995 must appear in the subject line.

The Academy of Natural Sciences is an Equal Opportunity Employer. Minorities, women and veterans are encouraged to apply.
]]> 2009-10-14T09:40:24-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1420815712.html text 2009-10-14T09:40:24-04:00 http://philadelphia.craigslist.org/sci/1419698939.html As a Marketing Manager you will be responsible for identifying and pursuing methods to create awareness of Company’s products and services to the market place. Specifically you will be:
• Planning, scheduling, and coordinating webinars
• Identifying, planning, and attending relevant tradeshows
• Identifying optimal print and web based advertizing channels and working with designers for product advertizing campaigns
• Managing web site design and content
• Responsible for design and production of all product collaterals such as fliers, white papers, etc.
• Responsible for coordination of product training sessions and workshops
• Interact with company partners in co-marketing activities.
• Responsible for product training materials as well as documentation
Qualifications:
• MS or PhD in a Life Science discipline.
• Minimum of 2 year previous marketing experience
• Strong knowledge of microarray data analysis (Copy Number, Expression, etc.) market is a MUST
• Excellent verbal and written communication skills, with the ability to clearly communicate highly technical information to both a technical and non-technical audience.
• Strong self motivation and personal organization skills. Ability to organize time and efforts to maximize results.
• Team player with an ability to work well independently with minimal supervision
• Travel less than 15%

This position can be home based. If you meet the qualifications above, please send CV and cover letter.]]> 2009-10-13T14:06:58-04:00 en-us Copyright &copy; 2009 craigslist, inc. http://philadelphia.craigslist.org/sci/1419698939.html text 2009-10-13T14:06:58-04:00