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Sr Engineer - 35760
mîrus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved.
Position Summary
The Sr Engineer provides advanced technical support for commercial manufacturing operations within a GMP-regulated pharmaceutical, biotechnology, medical device, or combination product environment. This role is responsible for supporting process performance, packaging operations, product quality, investigations, validations, and continuous improvement initiatives. The Sr Engineer collaborates with cross-functional teams to ensure manufacturing processes remain compliant, efficient, and capable of consistently delivering high-quality products.
Key Responsibilities
Position Summary
The Sr Engineer provides advanced technical support for commercial manufacturing operations within a GMP-regulated pharmaceutical, biotechnology, medical device, or combination product environment. This role is responsible for supporting process performance, packaging operations, product quality, investigations, validations, and continuous improvement initiatives. The Sr Engineer collaborates with cross-functional teams to ensure manufacturing processes remain compliant, efficient, and capable of consistently delivering high-quality products.
Key Responsibilities
- Direct experience providing technical or process-development support to commercial pharmaceutical, biotechnology, medical-device, or combination-product manufacturing operations.
- Experience managing projects
- Experience with sterile injectable products, prefilled syringes, autoinjectors, pens, or other drug-device combination products.
- Direct knowledge of packaging operations, including primary and secondary packaging, labeling, cartoning, and packaging-line troubleshooting.
- Proven ability to investigate inspection rejects, packaging defects, yield losses, equipment alarms, and process deviations using structured root-cause-analysis tools.
- Experience authoring or reviewing technical protocols, study reports, engineering assessments, investigation reports, risk assessments, work instructions, and change controls.
- Knowledge of process qualification and validation activities, including equipment qualification (IQ/OQ/PQ), process performance qualification, test-method validation, and continued process verification or process monitoring.
- Basic experience using statistical and data-analysis tools to assess process performance, including trend analysis, control charts, process capability, variability assessments, and establishment of monitoring limits.
- Direct experience with GMP-regulated manufacturing and quality-system processes, including deviations, CAPAs, nonconformances, complaints, change controls, and data-integrity requirements.
- Experience collaborating cross-functionally with Manufacturing, Quality Assurance, Quality Control, Engineering, Validation, Maintenance, Automation, Supply Chain, and Regulatory Affairs.
- Experience supporting process improvements, equipment upgrades, new product introductions, technology transfers, or implementation of new inspection and packaging technologies in a commercial environment.
- Ability to provide effective on-the-floor support, communicate clearly with operations personnel, and make timely, data-driven technical decisions while maintaining compliance and product quality.
- Doctorate degree in Engineering; OR
- Master's degree in Engineering and 2 years of Engineering experience; OR
- Bachelor's degree in Engineering and 4 years of Engineering experience.
- Normally for the 1st shift or 8Am to 5pm.