Engineer at QRC Group, Inc

Juncos, Puerto Rico, United States -

Full Time

Start Date

Immediate

Expiry Date

18 Dec, 25

Salary

0.0

Posted On

19 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Engineering, Pharmaceutical Processes, Biotech Processes, Validation Processes, Technical Writing, Computer Literacy, Problem Solving, Process Optimization, Equipment Maintenance, Reliability Engineering, Environmental Compliance, Data Analysis, Project Management, CAPA Management, Manufacturing Equipment Ownership, Troubleshooting

Industry

Staffing and Recruiting

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. Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions! Job Description As an engineer working within regulated manufacturing environments, you will be expected to apply technical expertise and problem-solving skills to support operational excellence and compliance. Under general supervision, provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects. Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of minor scope and complexity. Responsibilities •Manufacturing Equipment ownership at CMMS system (Work orders approval, closing, PM strategy, spare parts' definition/accuracy/updates), reliability and change control assessments and requirements. •Collaborate with Engineering Staff to ensure the best maintenance strategy on manufacturing equipment operations. •Responsible for enhancing system reliability focusing on equipment availability, downtime reduction and maintenance optimization. • Develop equipment performance metrics (availability, downtime, etc.) with emphasis on identifying equipment performance improvement opportunities. • Lead the implementation of equipment improvements project.s • SME (Subject Matter Expert) for systems regarding design, maintenance and point of contact during compliance operations. • Support equipment troubleshooting within the functional area or in the scope of technical expertise. • Support deviation process and define, Implement and own CAPAs associated to equipment within area of expertise Drives Environmental, Health and Safety compliance within the organization. Qualifications Master's degree or Bachelor's degree in Engineering & 2 years of Engineering experience Knowledge of pharmaceutical/biotech processes Familiarity with validation processes Bilingual (Spanish/English) Technical Writing Computer Literacy Additional Information All your information will be kept confidential according to EEO guidelines.

Responsibilities

The engineer will support operational excellence and compliance in regulated manufacturing environments by applying technical expertise and problem-solving skills. Responsibilities include equipment ownership, reliability assessments, and leading equipment improvement projects.