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!

Sr Engineer with experience in Manufacturing Operations 

Hands-on experience in process engineering, man

ufacturing 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.

• Doctorate or Masters + 2 years of Engineering experience or
  Bachelors in Engineering + 4 years of Engineering experience (Chemical, Mechanical, Industrial or Biotechnology Engineering)

• Strong communication, adaptability to change

   

• Bilingual (Spanish/English)​

Benefits

What We Offer

• Opportunities for learning, development, and professional growth.
• A collaborative and supportive work environment.
• The opportunity to work with industry-leading clients on impactful projects.

Your information will be kept confidential according to EEO guidelines.