craigslist | science/biotech jobs in chicago

Team Leader Quality (Carol Stream, IL)

2009-12-23T00:08:27-06:00

As one of North America's largest packaged food companies, ConAgra Foods nourishes consumers with leading brands. More than 95 percent of American households shop for and enjoy our respected consumer brands, which include Healthy Choice, Chef Boyardee, PAM, Slim Jim, Hebrew National, Reddi-wip, Egg Beaters, Hunt's, DAVID, Marie Callender's, Orville Redenbacher's, and Banquet. With $11.6 billion in net sales, approximately 30,000 employees and a presence in more than 110 countries, ConAgra Foods is a Fortune 500 firm positioned to innovate and win, now and in the future.

Along with competitive salaries and benefits, our employees enjoy opportunities for professional growth and a workplace that encourages initiative, fresh ideas and working and winning as a team. We're looking for the best people with the best talent. Build your career with us and be a part of building the new ConAgra Foods.

Assists in the management of quality control activities for all phases of production, personnel and laboratory operations. Schedules and assigns workloads; and maintains close rapport with production to identify, solve and prevent problems affecting quality. Directs product quality surveillance of manufacturing areas with possible HACCP monitoring, conducts periodic facility inspections and may perform daily bacteriological environmental inspections in critical plant areas; supervises special inspections for incoming materials, end-of-run products, etc. Coordinates with production in the monitoring of packaging lines for effective control of weights, metal detection, codes and product/package integrity.

Qualifications:

Supervision of the central lab and/or inspection labs personnel at the facilities.

Assure the labs are staffed properly and test results are precise and accurate.

Provide technical assistance and training to labs personnel. Develop and implement written procedures for quality programs.

Monitor and verify the HACCP plan?s CCPs.

Conduct safety trainings and audits.

Conduct GMP and sanitation audits of operations and warehouse areas.

Work with operations personnel on quality and safety issues.

Verify operations control systems are functional and being followed.

Place product on hold or release as needed.

Maintaining laboratory equipment in good working order and standardized to ensure optimal performance.

Assure good laboratory practices are followed and documented.

Evaluate and disposition of returned and damaged products.

Maintaining budget within current guidelines.

Customer complaints coordination.

Benefits:

B.S. degree in Microbiology, Food Science, Chemistry or related fields.

5-7 years experience in Food or Pharmaceutical Industry with 3-5 years supervisory experience.

Knowledge of laboratory activities to include microbiological testing not limited to SPC, Coliforms/E.coli, Salmonella, Listeria, Yeast and Mold, analytical testing to include moisture, color.

Thorough knowledge: Good Sanitation Practices (GSPs) and Good Manufacturing Practices (GMPs).

Familiar with BRC Consolidated Standards and certification is a plus.

High level of competency with manufacturing/inventory/traceability systems with advanced skills in PC use including spreadsheets and database experience.

Understanding of Statistical Process Control and statistical analysis.

Good verbal and written communication skills.

Ability to work in a team environment.

Must have strong Microsoft Office skills.

Sanitation background is a plus.

As we build our brands, we're building the team that will take our business to the next level. Our high-performance culture is based on simplicity, accountability and collaboration and offers exceptional career opportunities throughout the organization. Challenging positions at all levels offer opportunities in sales, marketing, manufacturing, supply chain, IT, finance, R & D and other areas. All of our positions offer opportunity for personal growth and financial reward.

ConAgra Foods is an equal opportunity employer, and we place a high value on the diversity of our employees, customers, consumers and vendors. We're looking for the best people with the best talent. You can build your career and be part of building the new ConAgra Foods. Visit us at www.conagrafoods.com.

To Apply for this position, please CLICK HERE

Great Teaching Opportunity - Chemistry and other sciences (All Chicagoland)

2009-12-21T15:11:35-06:00

The Princeton Review, the world�s leader in test preparation services, is seeking instructors for our MCAT classes throughout Chicagoland. We want instructors who will excel at helping students prepare and succeed on the MCAT. We are looking for smart, dynamic, and energetic communicators who are interested in a great part-time job. Benefits of teaching with TPR include:

� Great teaching experience
� Starting pay rate of $20 per hour with opportunities to earn more
� Flexible schedules

The quality of our teachers is a huge reason for our success. Our instructors must be enthusiastic, energetic, and sympathetic. We don�t lecture; we interact with students to make teaching and learning as fun and engaging as possible. In order to ensure high-quality instruction, we�ve developed our own high-quality training and certification process. No prior teaching experience is required!

In order to be considered for a position, candidates must:

� Have taken the MCAT and received qualifying scores; or have a verifiable mastery in one of the subject fields on the exam (Inorganic Chemistry, Organic Chemistry, Physics, Biology, and/or Verbal Reasoning)
� Attend an interview and demonstrate an outstanding teaching style
� Be available to teach evenings and weekends

Do not delay! Training and classes begin soon. Please send a current resume or CV that includes your MCAT scores or field of mastery to Troy Marshall at ChicagoTeachers@Review.com.

Manager Clinical Budget Analysis- Abbott Planning and Resource Group (Lake County, IL)

2009-12-21T12:42:01-06:00

At Abbott, we provide the perspectives and experience necessary to translate science into real solutions for patients in over 130 markets worldwide. Today, 72,000 Abbott employees are doing work that matters.

PRIMARY FUNCTION / PRIMARY GOALS / OBJECTIVES: Performs financial analyses and budgetary reconciliation of the clinical trial budgets for one or more Therapeutic Areas. Utilizes multiple financial and reporting systems including: contract database, budget database, payment tracking databases, and investigator budget determining software. Collects, summarizes, consolidates and verifies data from multiple sources for confirmation of budget source, variance from planned budget and resources, monthly budget tracking, reporting and reconciliation as well as regular aggregate review. Facilitates interpretation and understanding of data. Identifies issues, cost savings and adjustments and communicates to clinical study management scenarios for addressing them. Interfaces with Clinical Field Operations study management teams and Finance, Clinical Project Teams, CPRM, Abbott Affiliates, Clinical Research Organizations, and other functional areas to ensure full accountability of clinical study budgets and resource utilization.

ACCOUNTABILITY / SCOPE:
Responsible for managing assigned therapeutic area study budgets simultaneously. Accountable for meeting project objectives on schedule and within budget. Responsible for development and oversight of investigator grant budget process to ensure fair market value. Reviews key decisions impacting budget/timelines with senior CPRM Management, Finance, and GPT/study teams. Provides recommendations for resolution of budget variance issues. May manage other junior department members and oversee clinical analysis activities.

Basic Qualification:
- Minimum of 8 years combined experience in clinical research operations and/or financial analysis required.
- Familiarity with basic finance and accounting processes and techniques, as well as budgeting, contracting, and payment processes and systems for clinical studies.
- Expertise in clinical study costing, Investigator Grant budgeting systems, MS Office applications, including Excel, Word and PowerPoint required.
- Requires 1 to 2 years experience either supervising or managing people with demonstrated leadership skills.
- Candidates should be flexible, able to work with minimal supervision and have good analytical, organizational and team skills.

Preferred Qualifications: - Prefer Pharmaceutical or CRO experience. Requires ability to understand scientific, financial, business facts and metrics.

Through numerous local, national and international accolades, Abbott is regarded as an employer of choice for our commitment to workplace excellence. Our employees are given the tools to succeed, lead and grow, with challenging opportunities and work that makes a difference. Through our diverse healthcare businesses, we connect people and potential in ways that no other company can.

Discover a world of opportunities at Abbott.

EEO Statement:

At Abbott, we believe that diversity drives innovation. Innovative thinkers who are passionate about the work they do, Abbott employees are representative of the diversity of the patients we strive to serve every single day across the globe.

If interested, please apply online at http://track.jobviper.com/ViewJob.asp?id=654734-1660-5244

Project Associate (Northbrook)

2009-12-17T14:33:05-06:00

PROJECT ASSOCIATE

Summary: The Project Associate is an integral member of the Operations department, providing support and troubleshooting on various aspects of projects for the project teams.

Required Experience:
- Bachelor's degree preferred with one to two years of experience working in a client-based environment within the CRO, research or biopharmaceutical industries.
- This job requires a person to be highly customer focused with excellent computer skills, including proficiency with MS Office. This position requires organizational skills with a high attention for detail. The ability to work in a team environment, meet deadlines, and prioritize and balance work from multiple individuals is necessary.

Essential Duties and Responsibilities:
- Deliver a positive, memorable and meaningful service which exceeds the expectations of both the internal and external customer.
- Attend local investigator and project specification design meetings.
- Participate in study design meetings along with the Project Manager, including teleconferences and in-person client meetings.
- Liaise with UK and inter-departmental colleagues on project-related issues.
- Provide backup to the Project Managers (PMs) on project-related duties.
- Troubleshoot on live study issues for the Project Managers.
- Create end-user documentation, call flow charts and other study-related documents as necessary.
- Create unit testing for test plans and execute testing.
- Prepare and collate completed study validation packages for transfer to the UK for the Project Managers.
- Support the client testing process by being available to assist clients with any issues.
- Update Specifications and other study-related documentation as necessary.
- Communicate with clients as necessary on any aspect of the projects

Clinical Statistician for Exploratory Statistics (North Chicago, IL)

2009-12-16T11:57:17-06:00

Hello,

My name is Britt Kilgrow and I represent The Fountain Group. We are a staffing firm and we are currently seeking a Clinical Statistician for a very prominent client of ours. The position is located in Northern Chicago, IL.

If you are interested e-mail a Word version of your resume to: britt@thefountaingroup.com

The details for the position are as follows;

Statistician for Exploratory Statistics in AP Educational Qualifications:
Masters or Ph.D. in statistics and related disciplines, with coursework/experience in biochemistry Primary Function: Provide statistical consulting and computing support for projects in areas such as drug discovery, pre-clinical and clinical biomarker research (genomics, imaging, etc.), and for biomarker, PK and immunogenicity assays used in preclinical and clinical studies.

Basic Qualifications:
At least two years of related experience with demonstrated skills/accomplishments as a statistician. Applications are also welcome from recent Ph.D. graduates that have done research on some of the topics noted above, with training and practical experience during school work.
Expertise in statistical methodologies such as nonlinear regression, mixed effects models, multivariate analysis, robust statistics, predictive modeling, machine learning methods, etc.
Strong school work (e.g., dissertation topic) and/or relevant academic/industry experience on topics related to drug discovery, genomics and other applications mentioned above. Strong computing skills in R, SAS and other programming languages.

Preferred Qualifications:
Familiarity in web-based tool development, JAVA, Perl, Visual Basic, etc. Background in bioinformatics, biochemistry, and related subjects.
If you are interested in hearing more about the position please respond to this email with a Word version of your resume and a copy of your references.

Regards,

Britt Kilgrow
The Fountain Group
10012 North Dale Mabry, Suite 211, Tampa, FL 33618
britt@thefountaingroup.com
www.TheFountainGroup.com
NOTICE TO RECIPIENT: The contents of this e-mail message and any attachments are intended for the addressee(s) named in this message. This communication is intended to be and to remain confidential and may be subject to applicable client/employee and/or work product privileges. If you are not the intended recipient of this message, or if this message has been addressed to you in error, please immediately alert the sender by reply e-mail and then delete this message and its attachments. Do not deliver, distribute or copy this message and/or any attachments and, if you are not the intended recipient, do not disclose the contents or take any action in reliance upon the information contained in this communication or any attachments

Sr. Manager, Pharmacoepidemiology & Epidemiology (Deerfield Park, Illinois)

2009-12-15T10:40:48-06:00

The Sr. Manager provides consultation for and facilitating the systematic planning, collection, and synthesis of global pharmacoepidemiology information for all Takeda products in collaboration with among others Pharmacovigilance, Clinical Sciences, Regulatory Affairs, Medical Affairs etc. The following are key elements of the position's objectives:
� The incumbent provides global strategies and pharmacoepidemiology research plans to further the commercial and clinical objectives for the therapeutic area or product
� The incumbent directs globally the designs and conduct of qualitative and quantitative analyses of pharmacoepidemiology studies (cohort studies, case-control studies etc.) to generate data that are important for decision-making in each stage of a product's lifecycle

ACCOUNTABILITES:
� Direct comprehensive pharmacoepidemiology strategies to help achieve product strategic targets and objectives (includes Clinical, Pharmacovigilance, Regulatory and Commercial).
� Oversee natural history of disease studies to understand the inherent risks associated with the indications for which medications are approved or under development
� Translate the vision of pharmacoepidemiology in cross-functional objectives and activities
� Manage the use of longitudinal databases, SRS databases and literature
1) to develop an understanding of potential safety issues for new compounds and new indications, based on experience with related compounds, and
2) to contribute to position papers relative to marketed products
� Effective communication of pharmacoepidemiology plans and deliverables in U.S. and globally, both to internal and external audiences.
� Present pharmacoepidemiology data and evidence to regulatory agencies and advisors/opinion leaders and convey logic
� Partner with Clinical Sciences and Pharmacovigilance in clinical trial planning, creation and conduct of risk management strategies utilizing pharmacoepidemiology research techniques.
� Provide pharmacoepidemiology expertise during due diligence and make recommendation based on the findings
� Represent, Takeda at pharmacoepidemiology meetings, and relevant Regulatory Agency meetings
� Be an advocate for pharmacoepidemiology activities
� Set goals, supervise, and evaluate performance of staff as well as planning growth of personnel.
Qualifications
EDUCATION, EXPERIENCE AND SKILLS:
Education:
� Required: Masters in Pharmacoepidemiology, or Epidemiology, with minimum 8 years experience in the pharmaceutical industry, CRO health-related consulting company, or academia (or a combination of afore-mentioned)
� Preferred: PhD in Pharmacoepidemiology, Epidemiology, or MD with a Masters in Pharmacoepidemiology or Epidemiology, or PharmD with a Masters in Pharmacoepidemiology or Epidemiology with minimum 5 years experience in Pharmacoepidemiology, or Epidemiology, in the pharmaceutical industry, CRO health-related consulting company, or academia (or a combination of afore-mentioned).
Experience:
� Experience with risk management planning is desired.
� Ability to follow scientific arguments, identify pharmacoepidemiology scientific data needs
� Extensive experience with observational database analyses and methodologies
� Ability to obtain pharmacoepidemiology regulatory opinions, assimilate data effectively define an epidemiology regulatory strategy and communicate with FDA and other Health Authorities in meetings as required
� Ability to understand the market and regulatory challenges for Takeda products; and to critically review competitors' data and assimilate pharmacoepidemiology strategies that take such environments into consideration.
� Excellent qualitative and quantitative pharmacoepidemiology skills, including with regards to study design and analysis of health insurance claims and other automated healthcare databases.
� Familiarity with SAS or similar software for data manipulation and data tabulation
� Excellent problem-solving and interpersonal skills are required, as are a high degree of self-motivation, initiative and attention to detail.
� Ability to work independently as well as in a team, and to manage multiple projects under tight deadlines are also essential.
� Setting goals, supervising, and evaluating performance of staff as well as planning growth of personnel.
� Excellent scientific writing, technical skills.

TRAVEL REQUIREMENTS:
30% Required Domestic and International travel.

Quality Control/Food Production (Chicago, Near West)

2009-12-14T16:34:18-06:00

Our near west side fresh food production company is currently seeking a Quality Control Manager to evaluate, revise and manage our Quality Control plan. This position requires:
� MS degree in Food Science, Food Technology, Microbiology, Chemistry, Biology or related Science degree
� 4+ years QC Management role preferably in a fresh-food manufacturing environment
� Food manufacturing experience
� Demonstrated knowledge of USDA, FDA regulations
� Demonstrated experience in implementing quality tools, HACCP, GMP, SSOP
� Knowledge of AIB, sanitation and pest control principles, Fresh Food Production, MAP
� Laboratory testing and knowledge of shelf life and environmental test procedures
� Experience in supervising, coaching, and training of others required
and a minimum of four years experience.

The QC manager will be responsible for developing, implementing and monitoring the methods and procedures for continuous quality improvement in our fresh food production facilities. The QC manager will create and implement quality inspection and testing criteria and procedures, and establish the programs that monitor compliance with customer�s specifications, company policies and regulatory agencies. The incumbent supervises the company�s laboratory and monitor data on plant sanitation, pest control, GMP and SSOP

Bilingual in English and Spanish is not required, but would be considered a plus.
The employer offers health, dental, accident, short and long term disability and life insurance as well as a 401k plan, vacation and paid holidays.

Microbiology Laboratory Manager (Northbrook, IL)

2009-12-10T10:14:52-06:00

Microbiology Laboratory Manager

Company: Northland Laboratories, Northbrook, IL 60062
Status: Full Time, Employee Job Category: Laboratory

Job Description

Northland Laboratories is a complete solution provider of Quality Assurance and Research & Development services for the food and pharmaceutical industries, including Microbiology Testing, Chemistry Testing, Nutrition Labeling, Shelf Life Studies, Validation Studies, Challenge Studies, Regulatory Support, Methods Development, Consumer Research, and Sensory Evaluation.

Northland Laboratories works with many top-100 Food and Pharmaceutical companies in various services concerning Quality Assurance and Research & Development.

As an important member of our Management Team, you will:

Manage and lead the Microbiology Laboratory Department for testing services performed, interact daily with Manufacturers of Products on their laboratory testing and results, Advise and Consult Manufacturers on their test results and products, manage various projects concerning Shelf Life and Challenge Studies, evaluate new technologies and validate new test methods, oversee Quality Assurance activities in your department, perform audits of manufacturing facilities, help manufacturers on solving problems and assuring their quality.

Bachelor's or Masters Degree in Biology, Microbiology, or Food ScienceHACCP certification required.
Minimum 2-3 years functional managerial experience required.
Experience in food industry.
Prior experience in Microbiology laboratory testing, GLP, Shelf Life Studies, Challenge Studies, and Validation Studies.
Effective written and verbal communication skills. Effective computer skills.

An Equal Opportunity / Affirmative Action Employer

Contact Information

Company: Northland Laboratories

Apply here: http://www.northlandlabs.com/northlands/home_career.aspx

Field Chemist (Gary, IN)

2009-12-07T15:56:03-06:00

Experienced Field Chemist needed to perform lab pack work in the Gary, IN area. Must have 4 year college in Science/Chemistry or related field. Assist in the Segregation of chemicals by hazard class; packing compatible materials in appropriate containers and preparing for transportation; completing necessary paperwork per job. CDL class A or B is highly preferred as Chemist will transport samples to various locations. Prior labpacking or environmental waste experience preferred.

Research Technologist 1 (Chicago)

2009-12-04T15:23:11-06:00

One of the top-ranked universities in the country, Northwestern University, combines innovative teaching and pioneering research in a highly collaborative environment that transcends traditional academic boundaries. Northwestern provides students, faculty and staff with exceptional opportunities for intellectual, personal, and professional growth.

Job Summary:
Under direction, performs standard to moderately complex basic laboratory research procedures to analyze chemical/biological materials following a detailed research protocol. Responsibilities include maintaining murine colonies, performing animal surgical procedures, in vitro and in vivo imaging and microscopy.

Specific Responsibilities:
Follows detailed technical instructions in setting up and conducting standard experiments, including biological assays, quantitative and qualitative analyses;
Maintains detailed records of results; May enter data into computer for further statistical analyses; Manipulates resulting data and presents it in a variety of ways;
Maintains and provide detailed records of murine colonies;
Performs scientific literature searches as required;
May direct or instruct other laboratory personnel or students in research techniques and procedures;
Performs general laboratory maintenance tasks and inventories laboratory supplies;
Performs related duties as required or assigned

Minimum Qualifications:
Bachelor's degree in a basic science or the equivalent combination of education and experience from which similar skills and abilities may be acquired;
Experience with murine models of disease and prior mouse surgical experience required;
Previous experience with standard laboratory procedures and standard biochemical laboratory equipment;
Manual dexterity is essential for pipetting and for manipulating small instruments or tools;
Knowledge of scientific terminology;
Bachelor's degree in biological science;
Minimum 2 years of laboratory bench-work experience;
The ability to learn new techniques quickly and a strong interest in doing science are also required;
Organizational Skills;
Problem Solving Capabilities;
Ability to Multi-Tasking;
Animal Handling experience.

Preferred Qualifications:
3 years laboratory bench-work experience including experience with molecular biology techniques and murine models;
Experience with maintaining murine colonies, mouse surgical techniques; immunohistochemistry/immunofluorescence, confocal microscopy and other imaging techniques.
Research experience at Northwestern University;
Excellent Communication, Oral and Written skills;
Computer Proficiency;
Experience with Lab Animal Care;
Research Regulations.

To Apply:
Northwestern University offers a comprehensive benefit plan, including tuition discounts. All resumes for this position must be received through the electronic recruiting system. For consideration, please click on the link below. You will be directed to Northwestern University's electronic recruiting system, eRecruit, where you will search and apply for current openings. To apply for this position in eRecruit, enter the Job Opening ID number 15304 in the appropriate search field. Once you apply, you will receive an email confirming submission of your resume. For all resumes received, if there is interest in your candidacy, the human resources recruiter or the department hiring manager will contact you. Job Opening ID number for this position is # 15304.

http://www.northwestern.edu/hr/careers

Northwestern University is an Equal Opportunity, Affirmative Action Employer.

Full Time Research Assistant in Behavioral Medicine (Downtown Chicago)

2009-12-03T10:20:41-06:00

This position will be responsible for assisting with the coordination of a clinical research program focused on improving intervention for depression and other mental health problems. Current studies include telephone and internet based interventions for depression as well as other uses of technology to improve mental health care. This position will also be required to perform daily tasks independently with general direction from the Project Coordinator. This position may require some flexibility on work hours to accommodate patients.

Specific Responsibilities:

Performing subject recruitment, including identification of potential participants and initial screening;
Performing subject assessments;
Performing data scanning/entry, data monitoring, data reduction;
Participating in weekly research meetings;
Assisting the PI with other projects, including literature searches, etc;
Performing other related duties as required or assigned.

Minimum Qualifications:

A bachelor�s degree in psychology or related field, or the equivalent combination of education, training and experience from which comparable skills can be acquired;
Excellent academic record: GPA of 3.0 or above.
Basic interviewing experience;
One year of experience in a clinical research environment;
Strong organization skills;
Excellent computer skills;
Strong writing skills;
Good interpersonal skills;
Data management ability.

While the following experiences and qualifications are not required, they could be useful:

Experience in HTML / CSS / JS / SQL
Experience conducting psychological assessments;
Experience working in a hospital setting;
Ability to learn online web-based data collection, database management, and data analysis techniques.

Interested applications: please forward resume AND cover letter to northwesternstudy@yahoo.com
**Due to the large number of submissions, we will only be able to respond to qualified applicants who have submitted a resume and cover letter.**

Northwestern University is an Equal Opportunity/Affirmative Action Employer and does not discriminate against any individual on account of that individual's sex, race, color, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran, or national or ethnic origin; nor does Northwestern discriminate on the basis of sexual orientation or gender identity or expression.

Laboratory Coordinator (Evanston, IL)

2009-12-02T10:19:27-06:00

The Laboratory Coordinator provides customer service and support to researchers utilizing the specialized equipment at the Keck Biophysics Facility at Northwestern University. Responsibilities range from instrumentation and computer maintenance, training researchers on equipment along with administrative tasks such as accounting, ordering, billing, and corresponding with vendors.

Minimum Qualifications:

A bachelor's degree in Science or Engineering
Experience of being main point person to trouble shoot computer issues
Experience with one or more of the following techniques: HPLC, Fluorescence, CD or Absorption Spectroscopy, RT-PCR, DLS, Gel imaging and scanning. AUC.
Strong interpersonal, communication and organizational skills

Preferred Qualifications
1-3 years of experience maintaining and repairing scientific instruments and computers
Demonstrated ability to work as part of a small team

Please submit CV ( including contact information of 3 references / supervisors) and cover letter ( including salary expectations and potential starting date).

Note: Only complete applications submitted via email will be considered.
No phone calls please.

Technology and Patent Literature Research

2009-12-01T21:07:37-06:00

Immediate, Part-time, full-time, virtual: Earn potential rewards for scientific technical documents and develop valuable experience in the exciting field of patent literature research.

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.****

Project Manager (Northbrook IL)

2009-11-30T11:42:26-06:00

PROJECT MANAGER

Summary: In this role, the Project Manager coordinates all project development activities. These activities range from overall timeline management to specification development, project validation and through to project go-live.

The PM will oversee that projects are developed to the full satisfaction of our clients and in accordance with project timelines. The Project Manager is the primary client contact.

Required Experience:

- Project management experience working in the pharmaceutical or healthcare industry is required. Experience supporting clinical trials using IVRS technology is desirable.

- A strong client-focused attitude is required, along with strict attention to detail, the ability to work well under pressure, and excellent oral and written communication skills.

- Knowledge of systems development lifecycle and project planning concepts is key. Good computer skills, including use of Word, Excel, and PowerPoint are also essential, together with a working knowledge of databases.

Essential Duties and Responsibilities:

- Delivering a positive, memorable and meaningful service which exceeds the expectations of both the internal and external customer.

- Write the design specification and oversee the development of individual projects in accordance with client needs.

- Manage the project team�s activities and interact with Project Assistants, Technical Project Managers and Programmers in order to ensure quality, accuracy and the timely delivery of projects to clients.

- Guide the client to successful use of our product suite. Assist the client with any problems or questions they may have throughout the development phase, including implementing changes or suggesting necessary improvements to project specifications.

- Supervise the project testing and validation for quality control on assigned projects, adhering to our regulatory requirements at all times.

- Travel to client sites and investigator meetings to give presentations and/or training on our product.

- Ensure that documentation of validation is completed.

- Ensure that regular contact is made with the client to foster satisfaction with the product and the company.

- Support the training needs of the Project Associates.

- Communicate pertinent information with reference to design specification changes, ensuring an understanding of client requests across all team members.

- Develop a system that will create a timely and efficient workflow process, and identify and suggest necessary process improvements to fellow team members.

- Accountable for financial project tracking and control, including monitoring invoice actuals to contacted amount, change in scopes and monthly revenue recognition.

Please submit resume for immediate consideration

Chemical Engineer Wanted (Chicagoland Area)

2009-11-28T16:15:30-06:00

Chemical Engineer wanted for development of a product for a start-up company. Qualified candidates will be compensated immediatley following the finished product. Candidates must have knowledge of gels and chlorine - bleach reactions/testing.

Quality Control/Food Production (Chicago, Near West)

2009-11-26T09:25:05-06:00

Business development - Consultant in Medical Devices (Chicago)

2009-11-25T15:01:28-06:00

ORGANISATION
UBIFRANCE, the French Agency for international business development, is hiring a Business development consultant. Based in Chicago, he/she will be part of the US Life Sciences Team which is supervised by the Ubifrance San Francisco office.

We work in a fast paced, results oriented environment managed by a dynamic team. Our goal is to accelerate the development of French companies in the US by providing advice, access to market information and business leads to our clients. We are looking for a smart, passionate and driven individual to join our team in Chicago.

POSITION
You will be part of a consulting team of three who assists French companies and entrepreneurs to forge and develop their business in the US medical sector. You will focus primarily on the medical devices market.

Your responsibilities include:
- Providing French companies with information and advice about the US market (competition, regulatory environment, distribution networks, healthcare system, etc.);
- Assisting French companies in finding new partners/clients in the US;
- Organizing trade missions and seminars in the US to foster commercial and technological collaborations between US/French companies.

REQUIREMENTS
You should be confident in reaching and convincing decision makers to take action as you will work with entrepreneurs/companies CEOs. Strong analytical and project management skills are a must.

Skills and experience required:
- Bachelor's degree in a relevant field: medical, life sciences, healthcare, business administration or other majors that include courses in sciences and in business.
- An experience in sales/business development is a plus, ideally in a medical device environment. Knowledge of the regulatory requirements in the US market would also be a plus.

Qualities the candidate should have demonstrated:
- Strong ability to build a professional network;
- Excellent interpersonal and project management skills;
- Autonomous and pro-active but team player, client-centered, solid work ethic;
- Strong verbal and written communications skills;
- A good command of oral French required in order to communicate with French companies.

All applicants must be legally authorized to work in the United States (Green card or work permit). No exceptions.

CONTACT
Please send by email your cover letter and resume with �Business development - Consultant in Medical Devices� in the subject line for immediate consideration.