Sr. Quality Engineer

Marc Jacobs International, LLC; Juncos (PR); On-site; USD 65,000 - 90,000; Full time

Job summary

Marc Jacobs International, LLC is seeking an experienced quality engineering professional for manufacturing services in the medical devices sector. The role emphasizes developing and maintaining quality standards, collaborating with engineering and manufacturing, and leading inspection and testing programs.

The ideal candidate has a mechanical/biomedical/industrial/chemical engineering background, 5 years in medical devices, and is bilingual (Spanish/English).

Qualifications

• Bachelor’s Degree in Mechanical, Biomedical, Industrial or Chemical Engineering, and five years of exposure within the Medical Devices Industry.
• Bilingual: Spanish and English
• Soft Skills: Excellent teamwork skills

Responsibilities

• Develops, modifies, applies, and maintains quality standards and protocol for processing materials into finished products.
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
• Devises and implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
• Designs or specifies inspection and testing mechanisms and equipment.
• Conducts quality assurance tests.
• Performs statistical analysis to assess cost and responsibility for products or materials not meeting standards.
• Ensures corrective measures meet reliability standards and documentation is compliant.
• May specialize in design, incoming material, production control, product evaluation and reliability, inventory control, and/or research.
• Expertise in validation strategies and equipment qualification (IQ/CSV/OQ/PQ), process validation, cleaning validation, and cleanroom qualification in GMP environments.
• Strong knowledge of Quality Management Systems (QMS), including change control, risk management, nonconformance investigations, and assessment of quality impact from changes.
• Experience evaluating regulatory impact with facility modifications, equipment relocations, and process changes, ensuring FDA/ISO 13485 compliance.

Skills

Teamwork

Bilingual Spanish-English

Education

Bachelor’s in Mechanical/Biomedical/Industrial/Chemical Engineering

Tools

IQ/CSV/OQ/PQ

Job description

For engineering services in the Manufacturing area.

WHAT MAKES YOU A FIT:

The Technical Part:

• Bachelor’s Degree in Mechanical, Biomedical, Industrial or Chemical Engineering, and five(5)years of exposurewithin the Medical Devices Industry.
• Bilingual: Spanish and English
• Soft Skills: Excellent teamwork skills
• Shift: 1st and according to business needs.
• Experience in:
  • Equipment & Process Validation
  • Quality Systems & Change Control
  • Regulatory Compliance & Manufacturing Change Management

The Personality Part:

• Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients, and team members. In other words, being a customer service pro is one of your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to Be The Piece?

AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)

• Develops, modifies, applies, and maintains quality standards and protocol for processing materials into partially finished or finished materials products.
• Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
• Devises and implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
• Designs or specifies inspection and testing mechanisms and equipment.
• Conducts quality assurance tests.
• Performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards.
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
• May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control, and/or research.
• Expertise in developing, reviewing, approving and executing validation strategies and deliverables associated with equipment qualification (IQ/CSV/OQ/PQ), equipment decommissioning, process validation, cleaning validation, and cleanroom qualification activities in GMP-regulated environments.
• Strong knowledge of Quality Management Systems (QMS), including change control, risk management, nonconformance investigations, and assessment of quality impact resulting from equipment, facility, and process changes.
• Experience evaluating regulatory impact associated with facility modifications, equipment relocations, and process changes, ensuring compliance with FDA, ISO 13485, and applicable global regulatory requirements.

WHO WE ARE:

We are a Service Provider companydifferent from the rest. We pride ourselves on how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities, and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented, and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industryclients with top-notch quality talent.We're FITS!

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