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Form of workQuality Assurance Specialist
WHY DO YOU WANT TO WORK AT LIVEO RESEARCH?
- Career stability and opportunities for advancement
- Complete Benefit Package, medical, dental, vision, 401K with company match, Short Term Disability, Employee Life
- Generous 401K Match
Liveo Research is a global manufacturer of rigid packaging solutions with five locations worldwide. Our pharmaceutical manufacturing plant in Delaware City, Delaware is looking for a Quality Assurance Specialist.
Do you have experience in QA/QMS support functions and projects, well then, we have a position for you. Come join our team!
Key Accountabilities:
General QA Lab Responsibilities include:
Coordinates and supports QA / QMS Support functions and projects, including:
- Document Control Program (maintenance of, review and update of site Document Control activities; maintenance and update of Document Control Systems)
- QA Training requirements (Quality System and GMP / GDP Awareness and Communication – Onboarding, Annual and/or as required)
- QA Process Support (including updating / troubleshooting the Delaware OCS defect detection system, Pest Control Reviews and Support)
- Corporate Regulatory / Sustainability programs (Ecovadis)
- Supplier Management Support (NCRs – tracking, communication, root cause and CAPAs, close out and effectiveness follow up)
- Site Auditing activity support – including pre-prep, CAPA finding tracking, investigation-Root Cause—CAPA generation where needed and follow up tasks for:
- External based Customer / ISO related Audits
- Internal based ISO / Corporate Audits
- Site Internal Auditor participation
QA laboratory support (serve as a Backup in daily QA testing when needed)
Qualifications:
- Bachelor’s degree in a Science (Chemistry) or Engineering related discipline preferred
- Minimum of 1-3 years of experience in Quality Assurance / Quality Control / Quality Engineering / Production Management in a fast-paced GMP / GDP environment (Pharma Packaging experience would be a plus)
- Previous experience in Pharma related Quality Programs including GMP / GDP, ISO QMS systems (9001, 13485), Customer Support / Audits, Continuous Improvement, Regulatory, Compliance, Sustainability and Internal Auditing
- Previous demonstrated experience leading Root Cause – CAPA investigations
- Excellent organizational skills – ability to multitask, and develop, assign and follow up on quality related tasks with QA team members as well as carry out tasks as assigned – train other team members as needed.
- Demonstrated ability to work independently with minimal supervision and works well with other team members in team projects/ activities.
- Previous experience and solid understanding of QA test equipment preferred.
- Ability to create, read, train, and follow required QMS documentation (specifications, SOP / work instructions and test methods.)
- Strong working knowledge of mathematical concepts (including fractions, ratios, and proportions) and the ability to apply these in lab / practical situations.
- Demonstrated ability to analyze and interpret information.
- Available to work 8 to 12 hour shifts as well as cover overtime and weekend requirements as business needs dictate.
- Desire and capability to learn new tasks.
Background Check required
Drug Testing required
Drug Testing required
Liveo Research is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, genetic information, or any other characteristic protected by law.
