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ECHO Consulting Group

Validation and regulatory documentation for pharma

Senior Engineer

Process EngineeringConfirmed live in the last 24 hours
ContractJuncos, Puerto RicoNo salary listedIn-person

About the Job

Requirements

  • A doctorate, or a master's degree with at least two years of engineering experience, or a bachelor's degree in engineering with at least four years of engineering experience.
  • Strong knowledge of pharmaceutical and biotechnology processes, production, and engineering science.
  • Expertise in writing, executing, and managing validation protocols under GLP/GMP standards.
  • Hands-on operation and expertise in laboratory equipment and specific processes.
  • Ability to solve technical issues from routine to highly complex using scientific theory, calculations, and data analysis.
  • Ability to identify and deploy internal or external resources to resolve issues independently.
  • Experience managing project schedules and costs through execution and completion.
  • Ability to manage multiple projects and priorities simultaneously.
  • Experience supervising third-party contractors and vendors.
  • Track record in delegation, teambuilding, and collaboration across diverse working styles.
  • Skills in negotiation, persuasion, facilitation, and conflict resolution.
  • Proficiency in technical report writing and professional presentations.

Responsibilities

  • Independently characterize process optimization strategies and troubleshoot operational issues in operations, manufacturing, pilot plant, or capital projects environments.
  • Apply advanced and diverse engineering principles to design and implement major system modifications, experiments, processes, and capital projects.
  • Develop, organize, analyze, and present interpretations of results for operational issues or engineering projects of significant scope and complexity.
  • Complete complex or novel assignments requiring development of new or improved engineering techniques and procedures.
  • Develop engineering policies and procedures that affect multiple organizational units.
  • Supervise, coordinate, and review work of a small staff of engineers, associates, and/or technicians on an ongoing and project basis.
  • Employ advanced engineering techniques or modify advanced techniques within the area of engineering expertise.
  • Apply engineering principles and practices outside the area of discipline expertise to a broad variety of related assignments.
  • Determine methodologies as a peer-recognized engineering technology specialist in at least one area.
  • Apply mature engineering knowledge in planning and conducting projects.
  • Develop technical solutions to complex problems requiring ingenuity and creativity.
  • Work with research, manufacturing, process development, utilities, facilities, quality assurance, and validation departments to develop requirements and recommendations for large or highly complex system and facility modifications.
  • Work with project managers to complete design and engineering projects within schedule, budget, and quality constraints.
  • Coordinate consultants, architects, and engineering firms in developing standard design documents.
  • Develop departmental or project budgets encompassing multiple disciplines for an area within a project or an entire smaller project.

Desired Qualifications

  • Knowledge of packaging equipment.
  • Knowledge of designing new equipment processes.
  • Knowledge of engineering projects.
  • Knowledge of validations.
  • Experience in the medical device or pharmaceutical industry.
  • Bilingual ability in English and Spanish.

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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