Sr Engineer

ECHO Consulting Group; Puerto Rico; Sur place; USD 70 000 - 110 000; Plein temps

Résumé du poste

ECHO Consulting Group seeks an experienced engineer to lead pharmaceutical laboratory construction projects in Puerto Rico. You will drive design, execution, and commissioning, ensuring regulatory and quality standards are met.

The role requires a Bachelor’s in Engineering and 5 years of related experience, with strong leadership and communication skills to manage multidisciplinary teams and complex lab facilities.

Qualifications

• Bachelor's Degree in Engineering plus 5 years of engineering experience.
• Experience leading laboratory construction projects in pharmaceutical/biotech environments.
• Strong knowledge of GLP/GMP, validation, and regulatory compliance.
• Ability to coordinate multidisciplinary teams and communicate effectively.

Responsabilités

• Oversee full lifecycle of pharmaceutical laboratory construction projects from concept to handover.
• Develop engineering strategies focused on process optimization and compliance.
• Lead development and approval of engineering documents, drawings, and reports.
• Coordinate with consultants, architects, and internal stakeholders to integrate requirements.

Connaissances

Engineering leadership

Lab construction

Regulatory compliance

Cross-functional collaboration

Formation

Bachelor’s Degree in Engineering

Description du poste

ECHO Consulting Group is a leader in providing solutions for the pharmaceutical, biotechnology, medical devices, and food industries. ECHO Consulting Group delivers high-quality solutions in CQV, quality management, regulatory compliance, manufacturing support, and project management. We are committed to offering exciting career opportunities in a workplace that values trust, respect, teamwork, creative talent, enthusiasm, and diligence. We are looking for talented professionals who are passionate about quality, collaboration, and delivering results. We believe great talent deserves great rewards. That’s why we offer a competitive compensation package and professional development.

Summary of Role:

Independently leads and directs the engineering, design, and construction of laboratories within pharmaceutical or biotechnology facilities. Responsible for developing and optimizing processes and resolving operational challenges related to lab construction and fit-outs in cGMP-regulated environments. Applies advanced and diverse engineering principles to the design and implementation of lab facility projects of significant scale and complexity. Develops, organizes, and interprets technical data to ensure projects meet regulatory, quality, and operational standards.

Responsibilities:

• Oversee the complete lifecycle of pharmaceutical laboratory construction projects, from concept through design, construction, commissioning, and handover.

• Develop and implement engineering strategies focused on process optimization, compliance, and operational efficiency in laboratory environments.

• Drive the development of engineering policies and procedures to ensure all laboratory construction meets regulatory, industry, and corporate standards.

• Supervise, coordinate, and review work of engineers, associates, and technicians assigned to laboratory construction projects.

• Collaborate with internal stakeholders such as research, manufacturing, process development, quality assurance, validation, and facilities teams to gather requirements and translate them into project specifications.

• Serve as a subject matter expert for laboratory engineering methodologies, ensuring best practices and innovation in design and construction.

• Lead the development, review, and approval of detailed engineering documents, drawings, and technical reports related to lab construction.

• Coordinate the work of consultants, architects, and engineering firms, ensuring laboratory requirements and specifications are fully integrated throughout project phases.

• Develop and manage project budgets, schedules, and procurement strategies for lab construction and fit-out, ensuring delivery within scope, timelines, and financial plans.

• Ensure all construction activities support a safe work environment and compliance with cGMP, GLP, and other regulatory standards.

Shift: Administrative

Location: Manati, PR

Education:

• Bachelor’s Degree in Engineering + 5 years of Engineering experience

Preferred Qualifications:

• Proven experience leading laboratory construction or renovation projects within pharmaceutical or biotechnology facilities

• Deep knowledge of pharmaceutical/biotech facility and laboratory design, construction, and engineering standards

• Strong understanding of GLP/GMP, validation, and compliance in lab construction projects

• Hands-on experience selecting, installing, and qualifying specialized laboratory equipment and systems

• Advanced problem-solving skills related to technical challenges in lab environments

• Experience coordinating multiple projects and priorities in a regulated environment

• Strong vendor, contractor, and stakeholder management abilities, including negotiation and conflict resolution

• Excellent technical communication and report writing skills

• Demonstrated ability to lead multidisciplinary teams and foster collaborative project execution

Equal Employment Opportunity

ECHO Consulting Group, Inc. is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or membership in any other class protected by federal, state, or local law.

We assure you that your opportunity for employment with ECHO Consulting Group, Inc. depends solely on your qualifications.