MindMed
MindMed is a clinical-stage biopharma company developing novel products to treat brain health disorders
51 - 200
QA Specialist
August 14
🏡 Remote – Anywhere in California
MindMed
MindMed is a clinical-stage biopharma company developing novel products to treat brain health disorders
51 - 200
Description
• Reports directly to the Head of Quality Assurance (QA), supporting QA needs for GCP, GLP, GMP, and GVP areas of the business • Manages GMP Vendor Document archival • Manages routing of GMP controlled documents for review and approval in the electronic quality management system (eQMS) • Utilizes eQMS for quality workflows and for the effective tracking, trending, and reporting of quality data and information • Prepares agenda and minutes for Quality Assurance meetings and Information Systems Steering Committee meetings, as assigned • Performs other document organization and archival tasks as assigned • Assists with tracking and managing non-GMP external, internal, investigator site, CSR and TMF audit activities
Requirements
• Required: Associate’s Degree or higher. Preference will be given to applicants with Bachelor’s Degree or higher • Experience and expertise in document management and control • Proficient written and verbal communication skills • Proficient in use of Microsoft Office applications and email. Preference will be given to applicants experienced with electronic quality management systems and project management applications • Ability to collaborate effectively with cross functional team members and external partners • Ability to manage multiple QA activities across multiple programs and studies • A can-do attitude and excellent attention to detail
Benefits
• 100% paid health benefits including Medical, Dental and Vision for you and your dependents • 401(k) program with company match and immediate vesting • Flexible time off • Generous parental leave and some fun fringe perks!
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