This is a primarily onsite role aligned to North Carolina Location.
Local Candidates Only, No relocations. Role will be supporting standard business hours, 8 AM - 5:00 PM, EW to work 8 hour day
Oversight and management of analytical method validation, transfers and verifications. Individual will be responsible for working in all scientific areas of Quality Control to support method implementation for GMP use.
Position requires a high level of organizational and visual project management skills.
Individual will author and own documentation related to tasks such as SOP's, Protocols and project timelines. Knowledge of QC electronic systems, laboratory equipment and current GMP regulations for pharmaceuticals a must. Individual must be able to work independently.
Preferred individual will have experience working collaboratively in a global environment
Basic Qualifications
Doctorate degree OR Master degree and 3 years of experience OR Bachelor degree and 5 years of experience OR Associate degree and 10 years of experience OR High school diploma / GED and 12 years of experience
Top 3 Must Have Skill Sets:
Knowledge of method validation and transfer ownership
Clear and concise communication (written and spoken) including project Gantt tables
Knowledge of GMP QC ICH guidance
Pay Rate between $36 - $42/Hr on W2 based on experience.
"This posting is for Contingent Worker, not an FTE"