Reqd BS chemistry, pharmacology or related. Knowledge of organic, inorganic analytical chemistry; biochemisty; drug design evaluation development; advanced drug delivery systems; advanced PK and Tox; medicinal chemistry. MF, 95.
Must have knowledge of Human Physiology, Forensic Pharmacy, Pharmacognosy, Phytochemistry Applied Biochemistry.
High School Diploma, or foreign equivalent, plus two 2 years of laboratory technician experience or bench work.br br The experience, which may be gained concurrently, must also include each of the followingbr br 2 years of supervisory experience;br 2 years of experience with laboratory sample preparation and processing, setting up Read more…
Must have good writing skills. Must have overseen other legal personnel and worked with international legal teams. Must be familiar and have worked with the civil law system of law.
Minimum requirements Bachelors degree in Mechanical Engineering, Industrial Engineering, Quality Engineering, or related field of study plus 2 years in quality control, manufacturing supervision or related experience.br br Must have knowledge or experience with ISO9001, ISO9000, or ISO14000; Reading mechanical drawings with geometric dimension and tolerance; Supplier quality system auditing; Read more…
In lieu of 6 month work experience in the job offered, the employer will accept a 3 credit hours academic coursework related to Communication Theory and a 3 credit hours academic coursework related to Data Acquisition.
exp. must be progressive include Exp. must include digital logic design; simulation, LINT, logic equivalency checking, clock domain cross checking, synthesis, static timing analysis, DFT support; ASIC SoC development flow; Verilog; C or C; scripting languages, VCS compiler, Synopsys Cadence EDA tools; FPGA simulation; written and oral reportspresentations. Will accept Read more…
Requires a Bachelors degree in Industrial Engineering or related field plus four years of quality engineering experience. Four years of experience must include four years of experience with each of the following 1 FDA Quality System Regulation, ISO 13485, and the Medical Device Directive; 2 ISO 14971, experience in risk Read more…
requires knowledge of GDT training, PPAP process, and APQP process