Job Description
Note:
FULLY REMOTE -ANY WHERE IS US IS OKAY
Top 3 Must Have Skill Sets:
- Experience with complaint/ investigation process with medical devices***
- 4+ years of quality and manufacturing experience in biotech or pharmaceutical industry
- Bachelor’s Degree in a Science Field
- Ability to successfully manage workload to timelines
- Familiarity with basic project management tools
- Ability to negotiate a position after taking feedback from multiple sources
- Demonstrated ability to consistently deliver on-time, and high-quality results
- Ability to operate in a matrixed or team environment
- Quality and manufacturing experience in biotech or pharmaceutical industry
- Understanding of the applicable complaint processes
- cGMP Experience
Basic Qualifications
- High school/GED + 4 years [Job Code Discipline and/ OR Sub-Discipline] work experience OR ?-Associate + 2 years [Job Code Discipline and/ OR Sub-Discipline] work experience OR ?-Bachelor + 6 months [Job Code Discipline and/ OR Sub-Discipline] work experience?-Master  ?
Day to Day Responsibilities:
- Ensures quality of complaint records
- Execution of SOP requirements
- Evaluates subject matter expert assessments
- Escalates potential Quality issues to Management
- Ensure execution of applicable Systems and Processes is in alignment with Operating Standards
- Communicate and ensure alignment on priority decisions
PAY RATE : $32/hr. on W2
"This posting is for Contingent Worker, not an FTE"