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ECHO Consulting Group

Validation and regulatory documentation for pharma

Quality Engineer 2

Quality EngineeringConfirmed live in the last 24 hours
ContractHumacao, Puerto RicoNo salary listed

About the Job

Requirements

  • A bachelor's degree in Engineering.
  • Preferred: A bachelor's or master's degree in Mechanical, Industrial, or Electrical Engineering, or a related field.
  • Experience in FDA- or ISO-regulated manufacturing environments, including GMP compliance, inspection readiness, ISO 13485, CAPA, nonconformance management, change control, document control, and risk management.
  • Knowledge of validation and manufacturing processes, including equipment, process, product, and software validation (IQ/OQ/PQ), risk-based validation, and manufacturing controls.
  • Proficiency in problem-solving, risk assessment, and data analysis tools, including FMEA, 5 Whys, Fishbone, SPC, DOE, capability analysis, trending, and process monitoring.
  • Experience with quality and business systems such as Minitab, JMP, Excel, Power BI, and SAP.
  • Lean Six Sigma certification and automation or programming experience are preferred.
  • Works independently with general supervision on larger, moderately complex projects or assignments.
  • Sets objectives for own job area to meet project and assignment objectives, and contributes to completion of project milestones.
  • Addresses general problems and issues that may require understanding a broader set of issues or other job areas, but are typically not complex.

Responsibilities

  • Develop, modify, apply, and maintain quality standards and protocols for processing materials into partially finished or finished products.
  • Collaborate with engineering and manufacturing functions to ensure quality standards are in place.
  • Devise and implement methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
  • Design or specify inspection and testing mechanisms and equipment; conduct quality assurance tests; and perform statistical analysis to assess the cost of and determine responsibility for products or materials that do not meet required standards and specifications.
  • Ensure corrective measures meet acceptable reliability standards and documentation complies with requirements.
  • May specialize in design, incoming material, production control, product evaluation and reliability, inventory control, or research and development as they apply to product or process quality.
  • Make adjustments or recommend enhancements in systems and processes to solve problems or improve the effectiveness of the job area.

Desired Qualifications

  • Experience with FDA- or ISO-regulated manufacturing environments, including GMP compliance, inspection readiness, ISO 13485, CAPA, nonconformance management, change control, document control, and risk management.
  • Knowledge of validation and manufacturing processes, including equipment, process, product, and software validation (IQ/OQ/PQ), risk-based validation, and manufacturing controls.
  • Proficiency in problem-solving, risk assessment, and data analysis tools, including FMEA, 5 Whys, Fishbone, SPC, DOE, capability analysis, trending, and process monitoring.
  • Experience with quality and business systems such as Minitab, JMP, Excel, Power BI, and SAP.
  • Lean Six Sigma certification and automation or programming experience.

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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