Catalent

Pharmaceutical

Director,QualityEngineering

St. Petersburg, Florida, United States FULL TIME
The Brief

“Director, Quality Engineering at Catalent. Skills: Quality Engineering, GMP Compliance, Regulatory Affairs, Leadership. Lead GMP quality engineering strategies. Provide quality engineering oversight for manufacturing”

What You'll Achieve.

Ensure product quality; Ensure patient safety; Ensure regulatory compliance; Deliver regulatory confidence; Achieve operational excellence; Improve product quality; Improve operational efficiency

Industry & Context.

Pharmaceutical
Problems you'll solve

root cause analysis

What They're Looking For.

Must Have

Bachelor's degree in Engineering (Biomedical, Mechanical, Electrical, Industrial) or a related scientific discipline, Minimum of 10 years of progressive experience in a quality role within the pharmaceutical or biotech industry, at least 5 years in a leadership role, Deep technical expertise in GMP-compliant manufacturing environments, Thorough understanding of global regulatory requirements and standards (FDA, EMA, MHRA, PMDA), Experience leading quality transformation initiatives that deliver regulatory confidence and operational excellence, background in drug product manufacturing, preferably oral solid dosage forms, Ability to manage multiple projects and prioritize tasks in a dynamic environment, Excellent communication skills, both verbal and written, ability to write concise technical documentation

Nice to Have

Master's degree, Experience with PowerBi, CoPilot Studio, Agentic AI, Experience in softgel technology, Experience in ISO 13485, FDA 21 CFR Part 820, ASQ Certified Quality Engineer, Prior experience with BMRAM, Trackwise, Solid dosage or small molecule experience other dosage forms with relevant experience acceptable

What You'll Do.

Lead GMP quality engineering strategies

Provide quality engineering oversight for manufacturing

Apply Quality Risk Management principles

Oversee enhancement of change control system

Support deviation investigations

Strengthen data integrity controls

Develop risk-based monitoring and metrics

Drive digitalization and automation initiatives

Lead and mentor quality engineers

Drive continuous improvement initiatives

How You'll Work.

Team & Collaboration

Partner with cross-functional teams; Lead a group of quality engineers and validation specialists

Communication Scope

Excellent communication skills; verbal communication; written communication; write concise technical documentation

Process & Methodology

Manage multiple projects, Prioritize tasks

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