Supplier Quality Specialist

About LTS:

LTS Lohmann Therapy Systems is a premier, global Contract Development and Manufacturing Organization (CDMO) and partner the pharma industry trusts most to deliver innovative oral, transdermal, and intradermal drug delivery systems. From concept to market, launch to lifecycle management, we deliver single source oral and transdermal drug delivery solutions that power partners’ market advantage. Every one of our 1,000 plus members of the LTS family, across three continents, is focused on utilizing our collective strength and innovation to explore new therapeutic opportunities, maximize partner value and improve patient outcomes.

We Care.

We Create.

We Deliver.

Job Summary

Are you a detail-oriented Quality Assurance professional with a passion for ensuring product excellence?

Lohman Therapy Systems North America is seeking a dedicated Supplier Quality Specialist to join our dynamic Quality Assurance team. In this pivotal role, you'll be responsible for supporting the Supplier Quality Management team in ensuring that our suppliers meet the highest quality standards.

This is a full-time, on-site role that can be located in West St. Paul, MN or West Caldwell, NJ.

What You Will Do:

• Audit Support: Assist in the planning, coordination, and execution of customer and internal GMP audits.
• Supplier Qualification: Support the qualification and reassessment of suppliers, ensuring they meet our rigorous standards.
• Documentation: Maintain accurate and up-to-date documentation related to supplier quality, including audit reports, qualification records, and corrective action plans.
• Supplier Performance Monitoring: Track and analyze supplier performance data to identify trends and areas for improvement.
• Supplier Corrective Actions: Assist in the development and implementation of corrective action plans for suppliers who do not meet quality requirements.
• Quality Systems: Contribute to the maintenance and continuous improvement of our supplier quality management system.

Your Background:

• Bachelor's degree in science or related field
• 9+ years of experience in a Pharmaceutical or medical device environment, with at least 2 years in a QA/QC role
• Strong attention to detail and organizational skills
• Proficiency in Word, Excel, PowerPoint, and SAP
• Knowledge of industry standards, cGMP's, and regulatory requirements
• Excellent communication and interpersonal skills

We Offer

• Competitive compensation and benefits package
• Opportunities for professional growth and development
• A collaborative and supportive work environment
• The chance to contribute to improving patient lives

Join our team and make a significant contribution to product quality and regulatory compliance.

LTS is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.