Investigation Specialist

Zohorecruit; Caguas (PR); On-site; USD 65,000 - 95,000; Full time

Job summary

Zohorecruit in Caguas, Puerto Rico, seeks an Investigations Specialist with experience in regulated industries to perform thorough, detailed investigations and generate high-quality reports. The ideal candidate has a science background and five years in manufacturing investigations, and is bilingual in Spanish and English.

Availability to travel to the United States is required. Responsibilities include understanding the investigation process for manufacturing issues, identifying root causes of

Qualifications

• Bachelor's degree in Science and five (5) years of experience in manufacturing investigations.
• Background in biology or chemistry and investigations.
• Available to travel to the United States immediately.

Responsibilities

• Understand the investigation process as itapplies to manufacturing issues and complaints.
• Understand the processes and systems involved inthe manufacture of biopharmaceutical products.
• Investigate process deviations andatypical/out-of-specification results and identify root cause.
• Conduct investigations with strict adherence tothe applicable quality and compliance standards.
• Develop and document corrective and preventiveactions (CAPA) and verify their effectiveness.
• Coordinate with Subject Matter Experts (SMEs)across functions to gather and verify the information required for theinvestigation.
• Exercise judgment in developing practices,techniques, and evaluation criteria for obtaining results.

Skills

Bilingual Spanish/English

Education

Bachelor's degree in Science

Job description

Caguas, Puerto Rico | Posted on 10/07/2026

Investigations Specialist with experience in regulatedindustries and strong knowledge of complaints and deviation processes. Thespecialist will be responsible for performing thorough, detailed, and timelyinvestigations and for the generation of high-quality, timely investigationreports. Must be available to travel to the United States immediately.

Responsibilities:

• Understand the investigation process as itapplies to manufacturing issues and complaints.
  
• Understand the processes and systems involved inthe manufacture of biopharmaceutical products.
  
• Investigate process deviations andatypical/out-of-specification results and identify root cause.
  
• Conduct investigations with strict adherence tothe applicable quality and compliance standards.
  
• Develop and document corrective and preventiveactions (CAPA) and verify their effectiveness.
  
• Coordinate with Subject Matter Experts (SMEs)across functions to gather and verify the information required for theinvestigation.
  
• Exercise judgment in developing practices,techniques, and evaluation criteria for obtaining results.
  

Requirements

Bachelor's degree in Science and five (5) yearsof experience in manufacturing investigations.

Background in biology or chemistry andinvestigations.

Bilingual (Spanish / English).

Available to travel to the United Statesimmediately.