QRC Group, Inc

Pharmaceutical

SrEngineer

$105–145k ~AI est. Juncos, Puerto Rico, United States CONTRACT
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for executive candidates.

The Brief

“Sr Engineer at QRC Group, Inc. Skills: Manufacturing Operations, Process engineering, Regulatory compliance. Troubleshoot manufacturing issues. Implement corrective/preventive actions”

What You'll Achieve.

Deliver results

Industry & Context.

Pharmaceutical
Problems you'll solve

Problem-Solving Skills; Troubleshoot manufacturing issues; Root cause analysis

What They're Looking For.

Must Have

Bachelors in Engineering + 4 years of Engineering experience, Doctorate or Masters + 2 years of Engineering experience, Bilingual (Spanish/English)

Nice to Have

Chemical Engineering, Mechanical Engineering, Industrial Engineering, Biotechnology Engineering

What You'll Do.

Troubleshoot manufacturing issues

Implement corrective/preventive actions

Drive process optimization

How You'll Work.

Team & Collaboration

Operations teams; Quality teams; Maintenance teams

Communication Scope

Communication

Full Job Description

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. ## Qualifications * 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)​ ## Additional Information 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.

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