TekniPlex Benefits Overview

Ensures product quality and regulatory compliance in a medical-device manufacturing environment. Leads quality issue, customer complaint, and NCMR investigations; supports CAPA, NPI, product transfers, process validation, audits, operator training, risk management, and continuous improvement. Analyzes quality metrics and collaborates with Engineering, Production, Regulatory, and Supply Chain teams to resolve issues and maintain compliant, capable manufacturing processes.

Join TekniPlex's talent community to stay connected for future opportunities across various fields, contributing to innovative material solutions.

Leads global strategic accounts for TekniPlex MedTech Solutions, owning account strategy, revenue growth, retention, profitability, pipeline, executive relationships, and major commercial negotiations. Expands customer engagement across products, regions, business units, and manufacturing locations while coordinating cross-functional teams. Requires strong medical device or engineered manufacturing experience, commercial and financial acumen, technical understanding, negotiation skills, and the ability to influence global stakeholders. Travel of approximately 30–50% domestically and internationally is required.