This position will perform in a cGMP environment following FDA and ICH guidelines. Duties include but are not limited to method development, method and instrument validation, raw material, components, drug substance, finished product, and stability testing in accordance with cGMP regulations, regulatory filings and approved procedures.
* Perform analytical testing (40%) * Operate and maintain equipment (20%) * Participate in special projects, as necessary (20%) * Prepare and maintain reagents and reference standards (10%) * Record, report, and verify data as well as writing procedures (10%)
Location: US - Fort Worth, TX
Education: Bachelor of Science in Chemistry or related scientific discipline
Licenses/ Certifications: N/A
Experience: 3-5 years in a laboratory, GMP preferred
Competences: Ability to work and prioritize independently; strong computer and organizational skills; excellent oral and written communication; self-motivated; adaptable to changing priorities; positive attitude; quick learner; familiar with good documentation practices
Physical Demands: able to life 25-30 lbs; able to stand 3-4 hours at a time