I must really be dumb

I must really be dumb. I get a couple of emails a day with a message similar to the one copied in below. I must be missing something; I don't understand this at all.

Make recommendations to Corporate Drug Safety Committee, as required.
Good communication skills.
Those who have interest in doing quality projects and expand their carrier growth are welcome. Interact with pharmacovigilance units in countries.
Perform black-box, guerilla, and regression testing of software products as required.
Interprets and prepares virology data for regulatory submissions. Then they are transform into the rice plant for the transgene expression and finally their analysis.
Ability to read a lot of material and condense the information.
Prepare reports of PMS studies for regulatory submission. After the constructs are clone into the suitable vectors they are mobilised into the Agrobacterium Strain.
Those who have interest in doing quality projects and expand their carrier growth are welcome.
Candidates well versed with GLP, FDA and other regulatory requirements will be preferred. Incumbent will work closely with Sales and Manufacturing Departments, as well. The candidate will perform data entry, data clean up, and data loading to maintain and expand a commercially successful database of available chemicals.
After the constructs are clone into the suitable vectors they are mobilised into the Agrobacterium Strain.
Degree: Life science degree expected with particular focus on virology.
Experience in sterile cell culture procedures, cell processing is needed.
Ensure that the global pharmacovigilance database is updated periodically.
A HO licence is preferred. Solids and liquid dosage form experince.
Board certified or board eligible is preferred.
Solids and liquid dosage form experince. This position will be responsible for production of analysis datasets and specifications, well documented code, summary tables and some statistical analysis of data. Participate in company core data sheets and product label changes and medical interpretation of safety data for regulatory documents. Provide pharmacovigilance input on designated products. Apply results to bug tracking system. Those who have interest in doing quality projects and expand their carrier growth are welcome. Responsible for supporting pre-clinical and clinical development of HCV compounds. Interact with pharmacovigilance units in countries.
The job requires: Independent working to develop processes and molecules within challenging time targets. D in pharmaceutical sciences.
Manages clinical staff and clinical projects, including CROs and contract labs. Experience of setting up facilites for sterile and cytotoxic products.
Board certified or board eligible is preferred. To produce and manage material for a variety of scientific disciplines. Interact with bug tracking system to monitor fixes and retests.


Until Next Time
Fai Mao
The Blogger who Receives lots of Spam