Senior development engineering

Job Description 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. That’s why we offer a competitive compensation package and professional development.
To independently conceive, design, implement and advance scientific experiments, which contribute to the successful completion of goals and/or projects. Provides input to new processes to generate robust and reliable data. Functions as a lead scientific / technical resource or as a project leader.
Independently monitors or conducts experiments, studies, or a series of experiments/studies to advance projects or technologies
Provides advanced data analysis and interpretation, and assesses impact of data on the project and makes recommendations
Key contributor to an independent research/project team
May contribute to scientific journal articles or complex technical documents as lead author
Plans detailed procedures for defined projects, including timelines, milestones, methodological approaches, expected results and necessary resources.
Shift: Monday–Friday, 8:00 AM – 5:00 PM
Doctorate PhD OR PharmD OR -Master’s + 3 years of Scientific experience OR -Bachelors + 5 years of Scientific experience.
Experience supporting sterile drug product manufacturing within the pharmaceutical or biotechnology industry.
Hands-on experience with aseptic filling operations, process characterization, process validation (PPQ), technology transfer, and commercial process support.
Strong knowledge of GMP requirements, aseptic processing principles, contamination control strategy, and pharmaceutical quality systems.
Experience performing statistical analysis using JMP or Minitab and applying data-driven approaches to process optimization.
Ability to analyze manufacturing data, identify process trends, and recommend scientifically sound solutions.
Experience working in cross-functional teams with Manufacturing, Quality,
Engineering, Regulatory, and Technical Services.
Strong technical writing, communication, presentation, and project management skills.
Ability to independently manage multiple projects in a fast-paced manufacturing environment while supporting commercial readiness and continuous process improvement.
Experience with single-use technologies, filling equipment, and sterile manufacturing operations is highly desirable.
Be able to problem solve using the application of scientific theory.
Demonstrate skills in independently determining and developing scientific analysis and solutions.
Exercise considerable latitude in determining objectives of scientific work.
Demonstrate strong laboratory and project management skills.
Creative skills in the development of new hypotheses for scientific experiments.
Demonstrate knowledge of scientific relevance of targeted work.
Bilingual (English and Spanish).
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.