The responsibilities of the Quality Director are:
Oversees all aspects of QA/QC.
Oversees implementation and evaluation of quality assurance policies and procedures.
Oversees that current and new policies and procedures are carried out.
Oversees quality lab operations.
Assists in other duties as designated by the Company President.
Continuously evaluates pharmacy operations and determines need for change in procedures.
Serves as Management Representative in ISO Quality Assurance System.
Established in 1997, UPI has evolved into a leading compounding pharmacy providing high quality preparations to hospitals and surgery centers across the United States. Located in Temple, Texas, UPI has built a strong reputation on high standards of testing, quality and personal service provided to its clients.
Send resume and salary requirements to kwilson@upisolutions.com or fax to 254-933-0111.
Two years of tissue culture experience is required, no exceptions will be made. Preference will be given to those with retroviral or lentiviral vector experience.
Please visit the following link for job description and to apply.
Please do NOT contact the investigator directly.
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 Ones 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 citizens 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!
MS degree or a BS degree in Medical Technology or other science-related major
2+ years of direct experience in project management in a clinical laboratory setting, or equivalent combination of education, training, and professional experience that provides the individual with the required knowledge, skills, and abilities.
Excellent written and verbal communication skills.
Ability to work well in a team environment.
Superior time management, planning, and organizational skills.
Demonstrated analytical and technical writing skills.
Working knowledge of MS Office applications.
This is a full-time position with benefits. Qualified candidates should send their resume with salary requirements to jobs@rulesbasedmedicine.com. Please put Project Manager in the subject line.
Responsibilities
The responsibilities for this position include, but are not limited to, the following areas:
Record test sample information from customers
Run cell-based assays
Enter experimental data to our database
Write summary reports for test samples
Manage day-in and day-out for laboratory supplies and equipment
Maintain GLP documents
Record and update company policies
Responsibilities
The responsibilities for this position include, but are not limited to, the following areas:
Write and submit grants to government agencies
Run existing cell proliferation assays
Design and execute new assays or other experimental procedures
Assist in writing reports to contractors and government agencies
Manage laboratory activities
* 3 - 5 years with the OEM
* Capable of Software/Hardware/Wafer Handling systems repair, preventative maintenance & training
* Ability to work confidently independently without close day to day supervision
* Excellent customer service and customer satisfaction skills
* Ability to pass a complete background check and drug screening without failure
* Ability to work as a 1099 or full time employee
* 2 or 4 year degree in electromechanical systems or electronics
Responsibilities: Conduct a series of experiments to supply scientific information as a part of larger project. Experimental procedures include Western blot analysis (including Bradford assay and Coomassie staining), gel electrophoresis, maintenance of cell lines, DNA and RNA isolation, PCR, RT-PCR, protein isolation and purification.
Qualifications:
Work History: 1 to 3 years of molecular biology laboratory work experience
Laboratory Skills: Skills required in general molecular biology, cell culture and biochemistry techniques, including SDS-PAGE gel electrophoresis, Imumunoblot analysis, PCR, protein and RNA isolation, and ability to work with small laboratory animals.
Education/Certification: B.S. or equivalent in a life science discipline.