Salary
💰 $119,200 - $186,250 per year
About the role
- Provide Quality oversight of validation programs
- Review validation documentation for compliance with procedural and cGMP requirements
- Collaborate with cross-functional teams to meet project timelines
- Provide Validation guidance and training to other departments
- Act as a validation subject matter expert for audits
Requirements
- Bachelor's or equivalent engineering or related life sciences field
- 8+ years of validation-related experience; or equivalent combination of education and experience
- Familiarity with GMP guidelines and international regulations for APIs and drug products
- Proficient with MS Word, MS Excel, and computerized statistical tools
- Ability to write reports, business correspondence, and procedures.
- Health insurance
- 401(k) matching
- Paid time off
- Flexible work hours
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
validationcompliancecGMPdocumentation reviewreport writingbusiness correspondenceprocedures writingstatistical tools
Soft skills
collaborationtrainingcommunicationproject management