Industrial Production Managers jobs

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.

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