Job Description
SUMMARY :
Quality Systems consultant needed to support Quality Systems initiatives for a thriving biotech organization
DUTIES & RESPONSIBILITIES :
- Set up, manage and maintain document control standards, quality and workflow
- Provide training for document control and other quality systems functions
- Vendor management and oversight
- eQMS Administration
- Other duties, as required
QUALIFICATIONS & REQUIREMENTS :
8 years of life sciences QA & QC experience, including extensive experience and proven expertise in biotech Quality Systems, including training, document control, document QC and other Quality Systems functionsSolid understanding of and compliance history with ICH guidelines, ISO 9001 and / or ISO13485 and GMPGood written, verbal, interpersonal and training communication skillsExperience as a MasterControl eQMS AdministratorVendor management experienceRelevant Bachelor's Degree