Enter Job Description...
- Conduct routine preparations for stability, raw materials, in-process, microbiology / cleaning validation program and other requested testing according to Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements
- Complete projects with supervision and have a clear understanding of Good Laboratory Practices (GLPs), CGMPs, and other regulatory requirements
- Ability to exercise judgment and appropriately raises issues to QC management
- Key focus will be preparing solutions (mobile phase, diluent, etc) and standard / sample preparations
- Required to follow good documentation practices
- Works cross-functionally to complete projects and testing
The Ideal Candidate will have :
Bachelor s required in life scienceGenerally, requires minimal to no prior relevant work experienceDemonstrated knowledge of analytical equipment and instrumentation and working in a GMP environment is helpfulProven skills in coordinating and leading day to day tasks and working in collaboration to accomplish deadlines and objectivesEEO Employer
LanceSoft is a certified Minority Business Enterprise (MBE) and an equal opportunity employer. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. LanceSoft makes hiring decisions based solely on qualifications, merit, and business needs at the time.