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, plus a stimulating and collaborative work environment. We are committed in providing exciting career opportunities in a work environment that values trust, respect, teamwork, creative talent, enthusiasm and diligence.

• 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 time lines.
  

• 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.
• Filed experience in validation equipments.
  

Interested send your resume to [email protected]