3d ago
New

Specialist Quality Control 35983

PRPR·Juncosmid
Manufacturing & ProductionQuality Manager
0 views0 saves0 applied

Quick Summary

Overview

Inteldot has over 15 years of experience in the life sciences industry, with allocations across Puerto Rico, the United States, Europe, and Japan.

Technical Tools
Manufacturing & ProductionQuality Manager

Inteldot has over 15 years of experience in the life sciences industry, with allocations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.

Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources.

Requirements

~1 min read
  • Experience in Microbiology, HPLC, and analytical methods.
  • Experienced in Method Validation, Method Transfer, Method Qualification.
  • Experience in project management.
  • Scientific Data Analysis.
  • Strong knowledge in Microsoft Excel as a Tool for Data Analysis.
  • Sample Management.
  • Basic Knowledge on equipment preventive maintenance and troubleshooting.
  • Agile on prioritization of critical tasks.
  • Ability to develop inspection or qualification protocols in a short timeframe period.
  • Strong negotiation skills.
  • Good communication skills.
  • Able to work with multi-functional Teams.
  • Able to communicate effectively in both English and Spanish.
  • Responsible for providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise.
  • Resolve technical issues and troubleshoot for assays as necessary
  • Ensure lab compliance which includes Implementing procedures that enhance GMP, GLP and safety.
  • Manage existing and/or develop and implement new programs, processes and methodologies.
  • Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact.
  • Approve lab investigations, Lead audit teams
  • May serve as subject matter expert to develop technical training.
  • May perform routine work in a specific area of responsibility as necessary.
  • Represents the department/organization on various teams, independently responsible for following through on multi-site action items.
  • May interact with regulatory agencies regarding area(s) of responsibility including written responses.
  • May resolve issues with outside resources.
  • Doctorate OR Masters + 2 years of directly related experience OR Bachelors + 4 years of directly related experience OR Associates + 8 years of directly related experience OR High school/GED + 10 years of directly related experience.


Location & Eligibility

Where is the job
Juncos, PR
On-site at the office

About this job

Posted
3 days ago
Employer
has 33 open jobs on Jobera in 3 countries.

Listing Details

Posted
November 11, 2026
First seen
November 12, 2026
Last seen
November 13, 2026

Posting Health

Days active
1
Repost count
0
Trust Level
58%
Scored at
November 13, 2026

Signal breakdown

freshnesssource trustcontent trustemployer trust
Newsletter

Stay ahead of the market

Get the latest job openings, salary trends, and hiring insights delivered to your inbox every week.

A
B
C
D
Join 12,000+ marketers

No spam. Unsubscribe at any time.

Specialist Quality Control 35983