JT783 - MANUFACTURING ENGINEER II

Posted 2 Days Ago
Be an Early Applicant
Hiring Remotely in Villalba, PRI
Remote
Junior
Food • Healthtech • Biotech • Consulting
The Role
Designs and improves pharmaceutical manufacturing processes, production layouts, equipment installations, material handling, and operational procedures. Leads process validation, equipment IQ, and computer software validation activities. Inspects machinery performance, investigates deficiencies, conducts root cause analysis, incorporates inspection requirements, and supports corrective actions and statistical process control. Requires strong technical writing, communication in English and Spanish, collaboration, problem-solving, and continuous improvement skills.
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: 
  • In charge of Process Validation, Equipment IQ and Computer software validation.
  • Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.
  • Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.
  • Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
  • Adapts machine or equipment design to factory and production conditions.
  • May incorporate inspection and test requirements into the production plan.
  • Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
  • Develops manufacturing processes that are applicable to statistical process control and may develop those techniques. 

Qualifications:
  • Bachelor’s degree in Engineering 
  • Minimum of 2 years of relevant experience.
  • Process Validation, Equipment IQ and Computer software validation knowledge.
  • Technical writing knowledge and Communication skills
  • Experience in Investigation and root cause analysis
  • Collaboration and Teamwork with adaptability project tasks requirements.
  • Communication skills (English / Spanish)
  • Problem-Solving Skill and Continuous Improvement Mindset
  • Attention to details
  • Shift: 1st shift

Skills Required

  • Bachelor's degree in Engineering
  • Minimum of 2 years of relevant experience
  • Knowledge of process validation, equipment IQ, and computer software validation
  • Technical writing knowledge
  • Communication skills in English and Spanish
  • Experience in investigation and root cause analysis
  • Collaboration and teamwork skills with adaptability to project task requirements
  • Problem-solving skills and a continuous improvement mindset
  • Attention to detail
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The Company
HQ: Guaynabo, PR
23 Employees
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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