Pay - $53.00/HRto $63.00/HR depending on experience.

Job Description:

• Looking for someone with BS/MS degree. The person should be flexible and able to learn fast. Previous experience in process validation and writing GMP documents is highly desirable (1-2 years). Good writing skills. Proficient in word and excel. Should be able to work with transversal team. Also willing to go on shop floor and execute the studies following GMP and good documentation practice. This role will need to work with a transversal team, so interpersonal skills are important. Also time management since this role will have to work under strict timelines to meet project schedule. Should be willing to work flexible hours including evening/weekend (when needed, not routinely). Onsite.

Qualifications:

• BS or MS in basic sciences, math, engineering or pharmacy with 2 years’ experience or PhD with experience in biological processes or analytics in a cGMP environment.

About the Company:
The Fountain Group LLC