Validation Engineers/Specialists, Scientist, Quality Resources

ECHO ConsultingGroup; Caguas (PR); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Professional development

Collaborative work environment

Competitive compensation

Job summary

ECHO Consulting Group, located in Caguas, Puerto Rico, is seeking Validation Engineers/Specialists to join their dynamic team. The role involves integrating into cross-functional teams to support project activities, developing protocols, and analyzing data for client presentations.

The ideal candidate will have a Bachelor's degree in a related science, experience in FDA regulated environments, and excellent communication skills. ECHO offers competitive compensation and a supportive work culture.

Qualifications

• A minimum Bachelor's degree in a related science.
• Experience working in a FDA Regulated environment.
• Excellent verbal and written communication skills.

Responsibilities

• Integrate into a dynamic cross‑functional team.
• Develop and execute protocols following plant procedures.
• Analyze data and present conclusions to clients.

Skills

Good Documentation Practices

Technical writing

Analytical skills

Interpersonal skills

Project management

Education

Bachelor's degree in Engineering, Chemistry, Biotechnology or Life Science

Tools

Validation equipment

Job description

Validation Engineers/Specialists, Scientist, Quality Resources

ECHO Consulting Group is a highly successful and growing consulting company for the Healthcare industry for the last 12 years. ECHO offers professional development, training, competitive compensation, and a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in a work environment that values trust, respect, teamwork, creative talent, enthusiasm, and diligence.

Responsibilities

• Able to integrate into a dynamic cross‑functional team responsible for supporting/implementing activities.
• Develop and execute protocols and prepare final reports following plant procedures and regulatory requirements.
• Analyze data, and present conclusions and recommendations to clients.
• Organize, schedule and track projects in order to meet client requirements within agreed timelines.

Qualifications

• A minimum Bachelor's degree in a related science (Engineering, Chemistry, Biotechnology or Life Science).
• Experience working in a FDA Regulated environment.
• A thorough knowledge of Good Documentation Practices (cGDP), excellent verbal and written communication skills.
• Experience in writing technical documents, including validation documents (protocols and reports), assessments and investigations.
• Excellent interpersonal skills, coupled with a superb attention to detail, excellent review and analytical skills.
• Must have strong ability to organize and manage multiple tasks in a fast‑paced environment. The ability to work effectively with team members and work under minimal supervision.
• File experience in validation equipment.