JT473 - PROCESS ENGINEER I

Posted 5 Days Ago
Be an Early Applicant
Ponce
Junior
Food • Healthtech • Biotech • Consulting
The Role
As a Process Engineer I, you will recommend and implement modifications to equipment and processes to enhance quality and production efficiency. You will integrate equipment capabilities with process specifications, conduct statistical analyses, and ensure compliance with manufacturing regulations. You will also develop and validate manufacturing processes, support equipment installation, and collaborate with design teams to align processes with product needs.
Summary Generated by Built In

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

  • Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies, manufacturing techniques as well as production yields for existing or new products.
  • Integrates equipment and material capabilities to meet process module target specifications and technology target specifications.
  • Reviews product development requirements for compatibility with processing methods to determine costs and schedules.
  • Interacts with product design and development personnel to ensure that processes and designs are compatible.
  • May develop and conduct statistical analysis or recommend additions to document work.
  • Leads the innovation, development and/or optimization of new manufacturing concepts, processes and procedures for transfer to manufacturing operations
  • Develop, execute, and close protocols required as part of the validation lifecycle.
  • Supports equipment installation and assessment of inputs, outputs and alignment to requirements.
  • Ensures processes and procedures are in compliance with regulations.
  • Develops manufacturing processes that are applicable to statistical process control and may develop those techniques including the measurement systems.

Qualifications:

  • Bachelor’s degree in engineering
  • 2 years of relevant experience
  • Investigation and root cause analysis skills
  • Technical writing knowledge
  • Process Validation and Computer software validation knowledge
  • Equipment Validation
  • Fully Bilingual
  • Troubleshooting skills
  • Validation lifecycle
  • Availability for 1rst shift 

Top Skills

Engineering
The Company
HQ: Orlando, FL
23 Employees
On-site Workplace
Year Founded: 2011

What We Do

The Quality Consulting Group is a pharmaceutical, biotechnology, food and medical device specialty consultant that supports the manufacturing industry; services are provided in multiple areas including: Regulatory Compliance, Quality Operations, Validation, Manufacturing, Training and Technical Support. Starting, as individual services provider since 2002, Quality Consulting Group has supported clients implementing the latest standards such as Validation Guidance, ICH Guidelines, and Process Excellence and Risk Management tools.
Quality Consulting Group has provided expertise in such areas as: business, operational, quality, regulatory and manufacturing strategies; organizational structures; management controls; manufacturing and quality systems methodologies and practices; compliance programs; and accuracy reviews; FDA, EMEA and other regulatory matter

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