QA Tech – 2nd
Perrigo Company plc
full-time
Posted on:
Location Type: Office
Location: Allegan • Missouri • United States
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Job Level
About the role
- Respond to quality events and complete related documentation
- Determine immediate physical containment and remediation
- Assist in identifying, assessing, and containing defects
- Conduct ASP's and manage the rework process
- Provide rework instructions
- Review documentation and perform auditing of manufacturing and packaging processes for cGMP compliance
Requirements
- High school diploma or GED required, preference for advanced education
- Minimum of 2 years experience in an FDA regulated industry preferred, 6 months required
- Understanding of and ability to apply cGMPs
- Working knowledge of SOPs
- Strong analytical skills
- Excellent oral and written communication skills
- Strong interpersonal skills
- Ability to work independently against multiple deadlines
- Understanding of equipment operation and manufacturing/packaging processes
Benefits
- Competitive compensation
- Benefits tailored to supporting you and your family
- Career development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
cGMPSOPsquality event documentationdefect assessmentrework process managementauditingmanufacturing processespackaging processesequipment operation
Soft Skills
analytical skillsoral communicationwritten communicationinterpersonal skillsindependent worktime management
Certifications
high school diplomaGED