Quality Manager (Pharma Packaging) at Liveo Research – New Castle, Delaware
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About This Position
Why Join Liveo Research?
- Career stability with opportunities for advancement
- Comprehensive benefits package: medical, dental, vision
- 401(k) with generous company match
- Short-term and long-term disability, company-paid life insurance
About Liveo Research
Liveo Research is a leading global manufacturer of rigid packaging solutions, with five strategically located facilities worldwide.
Our pharmaceutical manufacturing site in Delaware City, Delaware is seeking a Quality Manager to join our growing team.
Position Summary
The Quality Manager is responsible for ensuring compliance with quality systems, regulatory requirements, and continuous improvement initiatives.
This role maintains a strong presence on the manufacturing floor, leading the development and execution of systems that prevent deviations and ensure consistent product quality.
The Quality Manager ensures all packaging materials meet customer expectations and comply with cGMP and regulatory standards, supporting business growth within the pharmaceutical sector.
Key Responsibilities
- Lead and execute quality strategy aligned with company and customer expectations
- Oversee day-to-day quality operations, ensuring compliance with cGMP, FDA, and ISO standards
- Maintain a strong floor presence to monitor, review, and improve quality systems and processes
- Lead investigations into deviations, complaints, and nonconformances; implement effective CAPA
- Ensure timely review and release of batch records, test results, and finished materials
- Develop, maintain, and continuously improve SOPs, policies, and quality systems
- Drive initiatives to reduce defects, complaints, and process variability
- Mentor, develop, and manage Quality team performance and training programs
- Ensure laboratory and testing practices meet global pharmaceutical standards
- Partner cross-functionally to support regulatory compliance and operational excellence
Minimum Qualifications
- Bachelor’s degree in Science, Pharmacy, or related field
- 7+ years of experience in pharmaceutical or biotech manufacturing within Quality
- Strong knowledge of cGMP, FDA regulations, ISO standards, and CFR requirements
- Proven ability to manage multiple priorities and meet critical timelines
- Excellent written and verbal communication skills
- Demonstrated leadership experience with team development and performance management
- Proficiency in Microsoft Office (Excel, Word, Project)
Preferred Qualifications
- Certified Quality Engineer (CQE) or equivalent certification
- Experience with Lean Manufacturing and/or Six Sigma methodologies
- Track record of driving cost savings and scrap reduction initiatives
- Experience in a multi-site or global manufacturing environment
Additional Requirements
- Background check required
- Drug screening required
Equal Opportunity Employer
Liveo Research is an equal opportunity employer and considers all applicants without regard to race, color, religion, sex, national origin, age, disability, veteran status, genetic information, or any other legally protected characteristic.