Iwona Normyle
Director, Analytical, Small Molecule AR&D, Microbiology at Merck
- Role
- Director, Analytical, Small Molecule Ar & d at Merck
- Location
- Bangor, PA, US
- LinkedIn followers
- 500 followers
About Iwona Normyle
Quality Control & Compliance Leader | 20+ yrs in QC, cGMP & GxP | Driving Excellence, Innovation & Digital Transformation | Building High-Performing Teams & Delivering Continuous ImprovementQuality Control professional with 20+ years of experience in QC, cGMP compliance, and GxP-regulated environments. Proven track record of leading cross-functional teams, managing labs and facilities, and implementing robust quality systems that meet global regulatory requirements. I am skilled in driving process optimization, automation, and digitalization to improve efficiency, reduce defects, and future-proof compliance.Recognized as a strategic and collaborative leader, I excel in aligning quality goals with business objectives, fostering a culture of innovation, accountability, and inclusion, and delivering measurable results in fast-paced, highly regulated industries.Core Competencies:• Strategic program & project leadership in dynamic environments• Critical decision-making aligned with compliance & business goals• Building, mentoring & transforming high-performing, diverse team• Empowering, people-first leadership that fosters collaboration and innovation• Driving accountability, ownership, and a culture of continuous improvement• Operational excellence with proven execution of strategic goals
Experience
Director, Analytical, Small Molecule Ar & d
Feb 2026 — Present · US
Education
UTP University of Science and Technology Bydoszcz, Poland, 1997
Masters Engineer’s Degree , Plant Pathology/Phytopathology
1992 — 1997
Skills
- Life Sciences
- Biotechnology
- Research and Development (R&D)
- Management
- Gmp
- Photoshop
- Leadership
- Powerpoint
- Microsoft Excel
- Medical Devices
- Capa
- Validation
- Research
- Microsoft Word
- Laboratory
- Gcp
- U.s. Pharmacopeia (Usp)
- Glp
- Usp
- Corrective and Preventive Action (Capa)
- Good Laboratory Practice (Glp)
- Training
- Microbiology
- Standard Operating Procedure (Sop)
- Microsoft Office
- Sales
- Pharmaceutical Industry
- Sop
- Fda
- U.s. Food and Drug Administration (Fda)
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