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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 listedIn-person

About the Job

Requirements

  • A master's degree, or a bachelor's degree in Engineering and 2 years of Engineering experience.
  • Provide problem-solving and applied engineering capabilities.
  • Have basic technical report-writing skills and verbal communication skills.
  • Have a comprehensive understanding of validation protocol execution requirements.
  • Provide basic technical presentations.
  • Have personal organization skills and validation protocol-writing skills.
  • Be able to deal with and manage change.
  • Have technical knowledge specific to equipment.
  • Have analytical problem-solving skills.
  • Have computer literacy.

Responsibilities

  • Provide solutions to technical problems of moderate scope and complexity.
  • Evaluate, select, and apply standard engineering techniques and procedures under general supervision, with assistance for unusual problems.
  • Perform assignments with clear and specific objectives that require investigation of a limited number of variables.
  • Initiate and complete routine technical tasks.
  • Troubleshoot operations as a technical expert for equipment or systems, becoming actively involved in daily operations as needed to meet schedules or resolve complex problems.
  • Routinely audit operational performance and regulatory compliance of a moderate number of significantly complex equipment items or systems.
  • 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 and 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 rudimentary project cost estimates and schedules.
  • Provide technical engineering support to continuous daily operations through troubleshooting, process optimization strategies, upgrades, replacements, and modifications to manufacturing processes or equipment.
  • Ensure operations comply with corporate policies, industry standards, and applicable regulatory requirements.
  • Support manufacturing operations on non-standard shifts, including nights and weekends, extended hours, and weekends as business needs require.
  • Function as a technical expert on processes, equipment, or systems during troubleshooting operations and cross-functional discussions.
  • Routinely supervise manufacturing processes for performance indicators and operations, suggest problem resolutions, and provide troubleshooting mentorship.
  • Support manufacturing and quality systems, including deviations, equipment qualification, process validation, procedures, training, and new product introductions.
  • Apply process, operational, and scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations.
  • Organize, analyze, and present interpretations of results for operational issues or engineering projects of moderate scope and complexity.
  • Apply basic engineering principles to the design and implementation of system modifications, experiments, or capital projects.

Desired Qualifications

  • Provide technical engineering support to continuous daily operations through troubleshooting, process optimization strategies, upgrades, replacements, and modifications to manufacturing processes or equipment.
  • Ensure operations comply with corporate policies, industry standards, and applicable regulatory requirements.
  • Support non-standard shift manufacturing operations, which may include nights and weekends.
  • Provide solutions to technical problems of moderate scope and complexity, evaluating and applying standard engineering techniques, basic principles, and procedures under general supervision, with assistance for unusual problems.
  • Function as a technical expert on processes, equipment, or systems during troubleshooting operations and multifunctional discussions.
  • Become actively involved in daily operations as needed to meet schedules or resolve sophisticated problems.
  • Routinely supervise manufacturing processes for performance indicators and operations, suggest problem resolutions, and provide troubleshooting mentorship.
  • Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance, and validation departments to develop requirements and recommendations for process or system modifications.
  • Support manufacturing and quality systems, including deviations, equipment qualification, process validation, procedures, training, and new product introductions.
  • Apply process, operational, and scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations.
  • Organize, analyze, and present interpretations of results for operational issues or engineering projects of moderate scope and complexity.
  • Apply basic engineering principles to the design and implementation of system modifications, experiments, or capital projects.

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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