Investigations Lead

QRC Group; Manatí (PR); On-site; USD 85,000 - 120,000; Full time

Job summary

QRC Group in Manatí, Puerto Rico, seeks an Investigation Lead to provide operational and scientific expertise in support of manufacturing sterile and non-sterile operations. The role manages manufacturing investigations (Quality Events) and coordinates information to support these investigations.

You will work on QE and CAPA trend evaluations, review regulatory submissions, and assist with regulatory inspections.

Qualifications

• Bachelor's degree in Science, Pharmacy, and/or Engineering.
• Five years of experience in a parenteral manufacturing facility.
• At least one year of experience in the investigation process.
• Strong technical writing and presentation skills.
• Ability to interpret and analyze statistical data.
• Knowledge of cGMPs, OSHA, EPA, and other regulatory standards.
• Proficiency with Microsoft Word, Excel, and PowerPoint.
• Excellent interpersonal skills and a teamwork-oriented approach.
• Excellent written and verbal communications skills in Spanish and English.

Responsibilities

• Ensure that all QEs, NTRs, and NOEs are completed and closed within the established timeframe, using the appropriate tools to prevent recurrence.
• Review and provide input to regulatory submissions applicable to the area of responsibility.
• Lead QE and CAPA trend evaluations.
• Participate in regulatory inspections when necessary.
• Support site initiatives and other assignments based on business needs.

Skills

Technical writing

Presentation skills

Statistical data analysis

Bilingual English/Spanish

Interpersonal skills

Teamwork

Education

Bachelor's degree in Science/Pharmacy/Engineering

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

Manati, Puerto Rico | Posted on 08/27/2026

We are seeking an Investigation Lead to provide operational and scientific expertise,together with compliance knowledge, in support of manufacturing sterile and non-sterile operations. The resource will execute manufacturinginvestigations (Quality Events, or QEs) and facilitate the collection andcoordination of information required to support those investigations.

Responsibilities

• Ensure that all QEs, NTRs, and NOEs arecompleted and closed within the established timeframe, using the appropriatetools to prevent recurrence.
• Review and provide input to regulatorysubmissions applicable to the area of responsibility.
• Lead QE and CAPA trend evaluations.
• Participate in regulatory inspections whennecessary.
• Support site initiatives and other assignmentsbased on business needs.
  

Requirements

• Bachelor's degree in Science, Pharmacy, and/orEngineering.
  
• Five (5) years of experience in a parenteralmanufacturing facility .
  
• At least one (1) year of experience in the investigation process .
  
• Strong technical writing and presentationskills.
  
• Ability to interpret and analyze statisticaldata.
  
• Knowledge of cGMPs, OSHA, EPA, and otherregulatory standards.
  
• Proficiency with Microsoft Word, Excel, andPowerPoint.
  
• Excellent interpersonal skills and ateamwork-oriented approach.
  
• Excellent written and verbal communicationskills in Spanish and English.