Quality Assurance Compliance Specialist
Kelly Science Engineering Technology Telecom · Clearwater, Florida, United States
FULL TIMEpermanent
Job Description
Quality Assurance Compliance SpecialistKelly® Science & Clinical is seeking a Quality Assurance Compliance Specialist for our client, a leader in the medical device industry, in Clearwater, Florida. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.Schedule: On-site Monday through Friday 8am to 5pmLength of assignment: until end of 2027Pay: $33-35 an hour
Below, you will find a complete breakdown of everything required of potential candidates, as well as how to apply Good luck.
Roles and ResponsibilitiesInspection Coordination: Prepare and execute inspections by regulatory agencies, consultants, and third parties.Organize CAPA Review Board meetings and Quarterly Management Review meetings.Regulatory Compliance Assessment: Identify improvement projects or CAPA through continuous assessment of the compliance environment.Regulatory Action Support: Assist with market actions, field alert reports, and other regulatory activities.Record Maintenance: Maintain thorough records of inspections, audits, and CAPAs, including root cause analysis and effectiveness checks.Quality Indicator Reviews: Provide documented reviews and recommend changes in product or process specifications.Quality Change Requests: Coordinate both temporary and permanent quality change requests.Internal Audits: Participate actively in internal audits.Administrative Support: Assist the Quality Department with various administrative tasks.Qualifications & SkillsEducation: Preferred Bachelor’s degree Life Sciences, Interdisciplinary Science, or Engineering.Experience: Minimum of 3 years in a GMP facility.MUST have experience in medical device industry and CAPA experienceIndependent and efficient work capabilities.Strong organizational and investigational skills.Ability to follow detailed procedures and multitask.Excellent analytical, problem-solving, and interpersonal skills.Proficiency in Microsoft Office (Word, Excel, PowerPoint).Exceptional written and verbal communication skills.
What happens nextOnce you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. xzbcwsv That means all of our recruiters will have access to your profile, expanding your opportunities even more.Helping you discover what’s next in your career is what we’re all about,#P1
Below, you will find a complete breakdown of everything required of potential candidates, as well as how to apply Good luck.
Roles and ResponsibilitiesInspection Coordination: Prepare and execute inspections by regulatory agencies, consultants, and third parties.Organize CAPA Review Board meetings and Quarterly Management Review meetings.Regulatory Compliance Assessment: Identify improvement projects or CAPA through continuous assessment of the compliance environment.Regulatory Action Support: Assist with market actions, field alert reports, and other regulatory activities.Record Maintenance: Maintain thorough records of inspections, audits, and CAPAs, including root cause analysis and effectiveness checks.Quality Indicator Reviews: Provide documented reviews and recommend changes in product or process specifications.Quality Change Requests: Coordinate both temporary and permanent quality change requests.Internal Audits: Participate actively in internal audits.Administrative Support: Assist the Quality Department with various administrative tasks.Qualifications & SkillsEducation: Preferred Bachelor’s degree Life Sciences, Interdisciplinary Science, or Engineering.Experience: Minimum of 3 years in a GMP facility.MUST have experience in medical device industry and CAPA experienceIndependent and efficient work capabilities.Strong organizational and investigational skills.Ability to follow detailed procedures and multitask.Excellent analytical, problem-solving, and interpersonal skills.Proficiency in Microsoft Office (Word, Excel, PowerPoint).Exceptional written and verbal communication skills.
What happens nextOnce you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. xzbcwsv That means all of our recruiters will have access to your profile, expanding your opportunities even more.Helping you discover what’s next in your career is what we’re all about,#P1
Details
| Company | Kelly Science Engineering Technology Telecom |
| Location | Clearwater, Florida, United States |
| Type | FULL TIME |
| Niche | healthcare |
| Experience | permanent |

