QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Engineering with experience in Manufacturing Operations. Hands-on experience in process engineering, manufacturing support, or production systems within a regulated environment (biotech, pharmaceutical, or similar).

Technical Knowledge: Familiarity with automation systems, process equipment, and continuous improvement methodologies (Lean Six Sigma, Kaizen, root cause analysis).

Problem-Solving Skills:  Demonstrated ability to troubleshoot manufacturing issues, implement corrective/preventive actions (CAPA), and drive process optimization.

Cross-Functional Collaboration: Proven experience working with operations, quality, and maintenance teams to deliver results in a fast-paced environment.

Regulatory / GMP Knowledge:  Understanding of cGMP, compliance, and documentation practices for regulated industries.

Additional Strengths – Strong communication, adaptability to change

• Master's degree or Bachelor's degree in Engineering & 2 years of Engineering experience (Background in Engineering disciplines, Chemical or Industrial Engineering, Biotechnology, or a related technical discipline).
• Bilingual (Spanish/English)(Write/Speak)
• Technical Writing
• Computer Literacy 

All your information will be kept confidential according to EEO guidelines.