Specialist Manufacturing - Juncos, PR - 35601

Integrated Services for Productivity & Validation, Inc

Juncos (PR)

On-site

USD 90,000 - 120,000

Full time

14 days+

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Job summary

Integrated Services For Productivity & Validation, Inc in Juncos, Puerto Rico is seeking a contract Manufacturing Operations Engineer. The role requires hands-on process engineering, manufacturing support, or production systems experience within regulated environments such as biotech or pharmaceutical sectors.

Applicants should have familiarity with automation systems, process equipment, and continuous improvement methods (Lean Six Sigma, Kaizen, CAPA).

Qualifications

  • Doctorate or Master's with 2+ years of Manufacturing Operations experience.
  • Bachelor's degree with 4+ years of Manufacturing Operations experience.
  • Associate's degree with 8 years of Manufacturing Operations experience.
  • High school/GED with 10 years of Manufacturing Operations experience.

Responsibilities

  • Hands-on engineering experience in manufacturing operations within regulated environments (biotech, pharmaceutical, or similar).
  • Familiarity with automation systems, process equipment, and continuous improvement methodologies (Lean Six Sigma, Kaizen, root cause analysis).
  • Troubleshoot manufacturing issues, implement CAPA, and drive process optimization.
  • Collaborate with operations, quality, and maintenance teams to deliver results in a fast-paced environment.
  • Understanding of cGMP, compliance, and documentation practices for regulated industries.
  • Strong communication and adaptability to change.

Skills

Engineering experience
Lean Six Sigma
CAPA
Process optimization
Regulatory/GMP knowledge

Education

Doctorate or Master's with 2+ years Manufacturing Ops
Bachelor's with 4+ years Manufacturing Ops
Associate's with 8+ years Manufacturing Ops
High school/GED with 10+ years Manufacturing Ops

Job description

Integrated Services For Productivity & Validation, Inc | Contract

Juncos, Puerto Rico | Posted on 08/05/2026

We provide the industry with a platform of solutions designed to their actual needs. We share and implement leading edge technology and methods that exceed customer expectation and deliver a one-stop provider of services focus on the well-being of the company and the employees.

Job Description
  • Engineering Experience in Manufacturing Operations – Hands-on experience in process engineering, manufacturing support, or production systems within a regulated environment (biotech, pharmaceutical, or similar).
  • Technical Knowledge – Familiarity with automation systems, process equipment, and continuous improvement methodologies (Lean Six Sigma, Kaizen, root cause analysis).
  • Problem-Solving Skills – Demonstrated ability to troubleshoot manufacturing issues, implement corrective/preventive actions (CAPA), and drive process optimization.
  • Cross-Functional Collaboration – Proven experience working with operations, quality, and maintenance teams to deliver results in a fast-paced environment.
  • Regulatory / GMP Knowledge – Understanding of cGMP, compliance, and documentation practices for regulated industries.
  • Additional Strengths – Strong communication, adaptability to change
Requirements

Candidates must have education, years of experience/expertise as follows;

  • Doctorate,or a Master's degree with 2 years of Manufacturing Operations experience
  • Bachelor's degree with 4 years of Manufacturing Operations experience
  • Associate's degree with 8 years of Manufacturing Operations experience
  • High school/GED with 10 years of Manufacturing Operations experience.

Preferred: Academic background in Engineering disciplines, particularly Chemical Engineering, Mechanical Engineering, Industrial Engineering, or Biotechnology.

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