Engineer

QRC; Juncos (PR); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Learning and development

Collaborative work environment

Work with industry-leading clients

Job summary

QRC Group, LLC is seeking an Engineer to provide technical support for continuous daily operations in a regulated manufacturing environment. You will troubleshoot, optimize processes, and upgrade equipment to sustain compliant operations, including nights and weekends as needed.

The role requires collaboration with manufacturing, QA, validation and other teams, ensuring adherence to corporate policies and regulatory requirements. Bilingual English/Spanish is essential.

Qualifications

• 2+ years of engineering experience in a regulated environment.
• Experience troubleshooting equipment and manufacturing processes.
• Knowledge of GMP and pharmaceutical/biotech manufacturing.

Responsibilities

• Provide solutions to technical problems of moderate scope and complexity.
• Function as a technical expert during troubleshooting and cross‑functional discussions.
• Supervise manufacturing processes and mentor operators.
• Collaborate with manufacturing, maintenance, QA and validation teams on upgrades and modifications.
• Support deviations, equipment qualification, process validation and training.
• Apply engineering principles to design and implement system changes.

Skills

Troubleshooting

Process optimization

Technical writing

Documentation

Cross-functional collaboration

Bilingual English/Spanish

Education

Engineering degree (Mechanical, Electrical or Chemical)

Job description

Company 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.

Job Description

We are seeking an Engineer that will provide technical engineering support to continuous daily operations by performing troubleshooting activities, process optimization strategies, upgrades, replacements, and modifications to the process or equipment in the manufacturing operations.

The professional must ensure that all operations are accomplished in a compliant manner consistent with current corporate policies, industry standards, and applicable regulatory requirements. This role will support non-standard shift manufacturing operations that may nights and weekends.

Specific responsibilities include but are not limited to:

• Provide solutions to a variety of technical problems of moderate scope and complexity. Under general supervision, will evaluate, select and apply standard engineering techniques, basic principles and procedures. Assistance given for unusual problems.


• Function as a technical expert to process, equipment and/or systems during troubleshooting operations and multi-functional discussions.


• Frequently become actively involved in daily operations when required to meet schedules or to resolve sophisticated problems.


• Routinely supervise manufacturing processes for performance indicators and operations. Suggest problem resolution and provide troubleshooting mentorship.


• Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for process and/or system modifications.


• Support the execution of manufacturing/quality systems such as deviations, equipment qualification and/or process validation, procedures, training, and new product introductions.


• Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations.


• Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of moderate scope and complexity.


• Apply basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects.

Qualifications

• Bachelor’s or Master’s degree in Mechanical, Electrical, or Chemical Engineering.


• Minimum of 2 years of engineering experience.


• Experience troubleshooting equipment and/or manufacturing processes within a regulated environment.


• Working knowledge of pharmaceutical or biotechnology manufacturing processes and GMP operations.


• Strong organizational, technical writing, and documentation skills.


• Excellent verbal, written, presentation, and communication skills in both English and Spanish.


• Ability to effectively communicate technical information and collaborate across multidisciplinary teams.

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.