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Manufacturing Engineer

EQVAL
Posted 15 days ago, valid for 16 days
Location

Ponce, PR, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • EQVAL Group, Inc. is seeking Manufacturing Engineers with a minimum of three years of experience in the Medical Device or Pharmaceutical industries.
  • The role involves executing validation protocols (IQ, OQ, PQ), troubleshooting, and optimizing manufacturing processes.
  • Candidates must hold a Bachelor’s Degree in Engineering and possess experience in developing validation documentation and conducting investigations.
  • The position is full-time and requires bilingual proficiency in English and Spanish, along with good technical writing skills.
  • Competitive compensation and benefits are offered, with the job located 100% on-site in South, Puerto Rico.

EQVAL Group, Inc. is a company that provides services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies, others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.

We are seeking Manufacturing Engineers with at least three (3) years of experience in Medical Device or Pharmaceutical industries. The role will focus on executing validation protocols (IQ, OQ, PQ), troubleshooting, and optimizing manufacturing processes.

Responsibilities:

  • Develop and execute validation activities for equipment and process changes (IQ, OQ, PQ) and associated documentation.
  • Optimize manufacturing processes, ensuring efficient production layouts, material handling, and tool fabrication.
  • Troubleshoot and improve production equipment and processes to enhance operational efficiency and product quality.
  • Collaborate with cross-functional teams to support investigations (NCRs, Complaints) and implement corrective actions.
  • Ensure compliance with regulatory standards (cGMP) in all manufacturing processes and validation activities.

Minimum Requirements:

  • Bachelor’s Degree in Engineering.
  • Experience in developing and executing validation documentation (Validation Plans, URS, FRS, IQ, OQ, PQ).
  • Experience in investigations (NCRs, Complaints, CAPA), Lean Manufacturing, and Six Sigma tools.
  • Experience with pFMEA (analysis and development) and its application.
  • Fully bilingual (English and Spanish) spoken and written.
  • Good technical writing skills.

*This opportunity will be full-time 100% on site in South, Puerto Rico.

*Remote and hybrid work arrangements are not available for this positions.

We offer competitive compensation, benefits, and opportunities for career growth. If you are a motivated individual with passion and ready to represent EQVAL Group, we would love to hear from you. Apply now!!

EQVAL Group is an EEO. We comply with all federal, local, and state laws regarding non-discrimination.




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