About this role
Sr. Compliance Specialist at Grand River Aseptic Manufacturing, Inc.. Location: Grand Rapids, Michigan, United States. Role: maintaining compliance, conducting audits, monitoring metrics Requirements: Bachelor's in Life Sciences; 10+ years QA/QC experience in pharma/biopharma/biotech manufacturing (or 5+ years plus GMP certification); proficient with Microsoft Word, PowerPoint, Excel, Outlook; technical writing; FDA regulatory knowledge; experience with electronic quality systems. Category: Quality Assurance Seniority: Senior Level Tools: Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook Certifications: gmp, asq, nsf Commitment: Full Time Workplace: Onsite Languages: English