1. Examining and analyzing cells, tissues and blood by collecting samples. For example, collecting blood samples to conduct blood tests.

2. Performing tests to look for microorganisms, parasites or bacteria in body fluids and blood.

3. Matching blood for blood transfusions.

4. Making specimens or samples to examine the count of cells in blood and abnormal cells in blood or body fluids.

5. Using microscopes and other sophisticated laboratory equipment to conduct tests.

6. Maintaining the laboratory equipment and ensuring that the laboratory is stocked well with all the necessary instruments.

7. Interpreting results and submitting the initial tests to the superior for further analysis.

8. Procuring up-to-date knowledge on technical developments in medical science.

9. Following science lab safety rules.

10. Performing laboratory tests in order to produce reliable and precise data to support scientific investigations.

11. Carrying out routine tasks accurately and following strict methodologies to carry out analyses.

12. Preparing specimens and samples.

13. Constructing, maintaining and operating standard laboratory equipment, for example centrifuges, titrators, pipetting machines and pH meters.

14. Ensuring the laboratory is well-stocked and resourced.

15. Recording and sometimes interpreting results to present to senior colleagues.

16. Using computers and performing mathematical calculations for the preparation of graphs.

17. Keeping up to date with technical developments, especially those which can save time and improve reliability.

18. Demonstrating practical procedures if working in education.

19. Conducting searches on identified topics relevant to the research.

20. Following and ensuring strict safety procedures and safety checks.

21. Analyze and record test data to issue reports that use charts, graphs and narratives.

22. Perform medical research to further control and cure disease.

Job Description 

CDL Truck Driver with C.R. England

 

Increase the size of your paycheck! C.R. England CDL Truck Driving Jobs Hiring Now!

Is your career in a slump?

Are you ready to get on the fast track?

Get started today in a new career as a CDL Truck Driver!

C.R. England, Inc. is NOW HIRING NATIONWIDE for over-the-road truck drivers to keep our company ranked #1 in the trucking industry! C.R. England is currently hiring individuals with no truck driver experience, experienced truck drivers and graduates from other truck driving schools.

C. R. England, Inc. is the nation’s largest refrigerated carrier and has been in business for over 90 years. We are well respected in the industry and known for our long length of haul and great equipment. C.R. England provides a safe, positive environment that fosters personal, career and financial success for driving professionals.

C.R. England offers:

 


Great Training

Top Pay

Top of-the-line Equipment

Strong Driver Support Program

Graduated pay scale -- experienced drivers earn higher base pay

Mileage, Safety and Fuel Saving Bonus Programs

Awards for safe driving

Liberal family rider policy

Health and life insurance

Vacation pay

Retirement plan 401k w/company participation



If you want an exciting career as a truck driver, C. R. England, Inc. is the place for you.

 

This established tannery group sells over 100 million square feet of leather throughout the world and is seeking to expand sales in the China region for domestic consumption.  Experienced and highly motivated individuals are welcome to forward CV to PrimeAsia at the following e-mail address; brightlee@yyhj.com.cn

 

Requirement:

a) Bachelors Degree and minimum 5years directly relevant work experience of leather 
b) Requires in-depth knowledge and experience in China domestic leather sales market
c) Uses best practices and knowledge of internal or external business issuesto improve products or services 
d) Solves complex problems, takes a new perspective using existing and creative solutions 

e) Work independently, receives minimal guidance 
f) Effective oral and written communication skills (Conversant in English Language). 
g) Computer skills

Our client is a very profitable, pharmaceutical company who is looking for a QA Supervisor to come in and make an impact. You will need to help hire, train, manage and coach assigned QA employees. You will also approve various documents and records. Ensure compliance with cGMP and company procedures. Communicate potential problems to senior management. Review and execute Batch Records as required, as well as review validation documents and control non-conforming materials. Ensure cGMP compliance in manufacturing, packaging and warehouse through informal and formal audits. You will communicate to senior management about supplier quality and production related issues as well as others that could potentially affect the safety, identity, strength, quality or purity of any product. Candidates must posses a BS degree. Solid dosage experience is also preferred.

Chemist/Microbiologist Needed in Waco, TX
  Kelly Scientific Resources is currently recruiting for several positions in Waco, TX QC Chemist – Contract Microbiologist – Direct HireChemist – Direct Hire Education and Experience:BS in Chemistry/Microbiology or related field is requiredWet Chemistry/HPLC Experience To apply please email your resume to lopezda@kellyscientific.com. Contact Information:Kelly Scientific ResourcesCentral TX210-384-8290lopezda@kellyscientific.com EOE

BASIC FUNCTION AND RESPONSIBILITY To participate in the design, execution and control of clinical research trials at the Clinical Trials Statistical & Data Management Center (CTSDMC); to coordinate the collection, analysis, processing, and reporting of data and to assist in judging the validity of test data obtained in the CTSDMC; to conduct on-site audits at participating centers worldwide; to develop new and/or revised CTSDMC procedures for clinical trial data management. CHARACTERISTIC DUTIES AND RESPONSIBILITIES Assist in the preparation of research papers and manuscripts for publication and presentation at conferences and workshops; assist in writing research progress reports, articles, and other documents, including summarizing recruitment and data collection results, adverse experiences, and safety issues. Coordinate design, development, and desktop publishing of newsletters for various trials; participate in writing and data reporting to be included in newsletters. Recommend data management areas to be explored, methods of analysis to be employed, and possible sources of data. Assist in design of data collection forms; prepare charts, graphs and other illustrations to facilitate the interpretation of clinical trial findings. Design and coordinate field tests for data collection forms and assist in design of certification procedures for participating clinical center staffs for designated trials. Develop procedures for and conduct on-site data audits at participating clinical centers worldwide; design and generate reports for use in data audits; summarize results of audits and write reports for the CTSDMC and funding agencies. Follow-up with centers to ensure corrective action post-audit has taken place. Coordinate meetings and training sessions for participating clinical center staff for designated trials. Prepare training materials and make presentations to clinical center staff for designated trials. Meet regularly with CTSDMC programming staff to explain specified trial design and to develop associated database design and data entry systems. Develop edit specifications for inter and intra case report form data checks for designated trials. Organize data search and analysis procedures associated with designated clinical trials; monitor patient recruitment and randomization in these trials; coordinate the processing of data from participating clinical centers; coordinate the processing of laboratory data from participating laboratories; coordinate and supervise central data entry and develop associated procedures. Responsible for the development and coordination of the processes of error resolution at participating clinical centers for designated clinical trials; develop and supervise error correction and documentation procedures at the CTSDMC. Develop CTSDMC procedures for various components of each trial's data management; document procedures for use in manuals, reports, or meetings. Participate in the development of general goals for designated clinical trials and in the planning of procedures for project completion. Monitor the progress of designated trials, identify potential problems, and recommend action. Plan and coordinate the work of graduate students, and other support personnel; and serve as a consultant to the project director, faculty and staff. Organize data for, and assist in writing of, proposals for new funding.

The assignment is flexible depending on capability and initial delivery on expectations.  Daily activities include batch weighing, batch making, stability testing, filling samples, getting raws, including proper documentation and control for raw materials and batches.
 
Scope
 
Assist in new product development for moisturizers within the skin care category. Develop and commercialize breakthrough exploratory products and bring them to a level of commercial preparedness so that they may be considered by the business.  Ensure physical and active stability, preservation, efficacy, consumer appeal, process ability, cost effectiveness, product/package compatibility.  Ensure formula complies with internal safety guidelines as well as external laws and regulations. Ensure Technology Transfer to design.
 
 
 
Challenges

- Multi-task management, ensure delivery of actions against aggressive timetables, achieve shared goals
- Maintain flexibility with respect to project directions
- Effectively manage information flow within the team
-Physical Requirements.
*Walking, standing for 3-5 hours continuously, light lifting (e.g. under 50 lbs).
*Operation of equipment (e.g. mixers, homogenizers).
 
 
 
 
 

This position is open as of 1/8/2010.

R&D Scientist - Food Microbiologist

R&D Scientist - Food MicrobiologistIf you are a R&D Scientist with food pathogen detection testing experience, please read on!We are one of the leading manufacturers of human rapid diagnostic tests and have expanded our products to include rapid tests of veterinary use and food pathogen detection. We have an immediate need for a PhD level microbiologist to lead the R&D development efforts on a new line of food pathogen detection tests.What you need for this position:- PhD in Microbiology or related- 5+ years of industry R&D experience in food pathogen detection testing- PCR-based food pathogen testing required- Loop-mediated isothermal amplification method experience preferred- AOAC testing/certification experienceWhat you'll be doing:- Responsible for R&D related to food pathogen detection testing- Identify new product opportunities- Collaborating with executive staff- Refining existing product lines based on market/client feedback- Managing the R&D process from concept to commercializationWhat's in it for you:- Competitive pay and benefits- Join a great company- Excellent career opportunities and potential for growthSo, if you are a R&D Scientist with food pathogen detection testing experience, please apply today!Required SkillsFood Microbiologist, PCR based food pathogen testing, Loop-mediated isothermal amplification, AOAC testing/certification,
If you are a good fit for the R&D Scientist - Food Microbiologist position, and have a background that includes:Food Microbiologist, PCR based food pathogen testing, Loop-mediated isothermal amplification, AOAC testing/certification, and you are interested in working the following job types:Science, Biotech, PharmaceuticalWithin the following industries:Biotechnology, Chemical, PharmaceuticalOur privacy policy: Your resume and information will be kept completely confidential.Looking forward to receiving your resume through our website and going over the job in more detail with you!

Sr. Polymer Chemist Needed for Direct Hire Position in East Tennessee! Kelly Scientific Resources is currently seeking a Sr. Polymer Chemist for a manufacturing company outside of Chattanooga, TN. The candidate will be responsible for product development including modifying existing formulations for improved performance and development of monomers and polymers for engineering applications. QUALIFICATIONS: - B.S. in Polymer chemistry with emphasis on organic synthesis or silicone chemistry. Advanced degree is preferred.- 5-10 years industrial experience in design and manufacturing of polymers.- Familiar with engineering polymers and structure/effects relationships.- Ability to support monomer and polymer production.- Must be team player and able to communicate with all levels of company personnel. If you meet the above qualifications, please APPLY now! Qualified candidates will be contacted immediately. Kelly Scientific Resources has grown into a $270 million global business as the scientific business unit of Kelly Services. Our staff of scientists provides scientific staffing to a broad spectrum of industries including: chemical, cosmetics, food, pharmaceutical, biomedical, consumer products, environmental, medical device, medical laboratory, petrochemical, and clinical research. We invite you to bookmark our Web site and encourage you to review it regularly for new opportunities worldwide: www.kellyscientific.com. Kelly Services is an Equal Opportunity Employer.

The Scientific Associate II will provide technical expertise in the R&D, design, measurement, installation, and commissioning of insertion devices for the National Synchrotron Light Source II Project.  Responsibilities will include designing and testing the electrical systems and controls interface for insertion device magnetic measurement facility.  Candidate will report to the NSLS-II Insertion Devices Group Leader.