Our unwavering commitment to quality ensures the delivery of safe and effective products to patients through a flexible, innovative, and customer-oriented culture rooted in science and risk-based compliance
Job Summary
Our unwavering commitment to quality ensures the delivery of safe and effective products to patients through a flexible, innovative, and customer-oriented culture rooted in science and risk-based compliance.
In this role, you will perform analytical method transfer, validation, verification, and support regulatory submissions while ensuring adherence to GMP and GLP standards.
You will contribute to continuous improvement initiatives, conduct training for colleagues, and participate in laboratory investigations to uphold a high-quality culture that adapts to meet patient needs.
Matching Summary
Our unwavering commitment to quality ensures the delivery of safe and effective products to patients through a flexible, innovative, and customer-oriented culture rooted in science and risk-based compliance.
Skills & Requirements
Must-have
Analytical Method Transfer and Validation
Good Manufacturing Practices compliance
Laboratory Investigations and CAPA
Analytical Testing using QC Instruments
Regulatory Submission Support
Data Integrity and ALCOA Principles
Nice-to-have
Experience with HPLC and GC techniques
Lean manufacturing and Six Sigma knowledge
Continuous Improvement Project Leadership
Strong problem-solving and attention to detail
Adaptability and willingness to learn
Use of AI tools for productivity
Effective interpersonal communication
Key Requirements
Bachelor's degree or equivalent experience
Demonstrated technical skills in method transfer and validation
Knowledge of Good Manufacturing Practices
4+ years relevant experience with Associate degree or 6+ years with high school diploma