Chemist I

Description:
RESPONSIBILITIES:
Maintains and supports the production schedule

Investigates problem areas and areas of desirable improvement
Undertakes new procedures and observes proper safety precautions
Responsible for in-process QC testing of manufacturing material as it relates to
qualifications, quality inspections and titration.
Maintains quality systems and proper GMP/GLP
Creates and follows protocols designed around product improvement
Responsible for making critical and non-critical bioreagents for use in product and
manufacturing processes using Standard Operating Procedures (SOPs).
Works in a team setting and coordinates manufacturing efforts based upon a set
production schedule and maintaining the raw bioreagent supply as needed to support
this schedule.


BASIC QUALIFICATIONS | EDUCATION:
Bachelor's Degree in a Chemistry, Life Sciences, or related field or equivalent
combination of education and experience.
Prior Experience in the following areas:
o Pipette
o Spectrophotometry
o HPLC
o pH meters
o Gel Electrophoresis o SDS Page
o ELISA assays

COMPETENCIES:
Ability to work successfully as a member of a team and independently with moderate
supervision.
Skill in using computer applications including spreadsheet, database, manufacturing, and
word processing software.