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ECHO Consulting Group

Validation and regulatory documentation for pharma

Engineer

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
ContractJuncos, Puerto RicoNo salary listed

About the Job

Requirements

  • A Master's degree, or a Bachelor's degree in Engineering and two years of Engineering experience.
  • Experience in biotechnology processes, specifically purification operations, is preferred.
  • Knowledge of chromatography and ultrafiltration/diafiltration techniques is preferred.
  • Skills in problem-solving and applied engineering are required.
  • Basic technical report-writing skills, verbal communication, and a comprehensive understanding of validation protocol execution requirements are required.
  • Basic technical presentation skills are required.
  • Personal organization and validation protocol-writing skills are required.
  • Ability to deal with and manage change is required.
  • Equipment-specific technical knowledge is required.
  • Analytical problem-solving skills and computer literacy are required.

Responsibilities

  • Provide solutions to technical problems of moderate scope and complexity.
  • Evaluate, select, and apply standard engineering techniques and procedures under general supervision, seeking assistance for unusual problems.
  • Perform assignments with clear, specific objectives that require investigation of a limited number of variables.
  • Initiate and complete routine technical tasks.
  • Serve as a technical expert for equipment or systems, troubleshoot operations, and become actively involved in daily operations when needed to meet schedules or resolve complex problems.
  • Routinely audit operational performance and regulatory compliance for equipment items or systems of significant complexity.
  • Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance, and validation departments to develop requirements and recommendations for system modifications.
  • Complete design, engineering, and construction projects under direct supervision of project managers, within schedule and budget constraints.
  • Work with consultants, architects, and engineering firms to develop standard design documents.
  • Obtain and critique quotes for equipment modifications or installations.
  • Generate basic project cost estimates and schedules.

Desired Qualifications

  • Experience in biotechnology processes, specifically purification operations.
  • Knowledge of chromatography and ultrafiltration/diafiltration techniques.

About the Company

ECHO Consulting Group

Validation and regulatory documentation for pharma

Echo Consulting Group provides specialized validation and regulatory documentation services for the healthcare, pharmaceutical, and biotechnology industries. Its offerings include process, cleaning, equipment, and computer systems validation, paired with regulatory compliance work and audit-ready documentation that meets cGMP and FDA requirements. The firm differentiates itself through long-standing expertise since 2002 and its integration into PharmaLex, which expands access to global resources while keeping its technical focus. Its goal is to help life-sciences organizations achieve regulatory success and efficient validation by delivering reliable documentation and support for validation efforts.

Company size
Not listed
Company stage
Not listed
Total funding
Not listed
Headquarters
Caguas, Puerto Rico
Founded
2002

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