QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusias...
Tittle: Senior Specialist QA – ProQN-711 Location: Juncos, Puerto Rico Work Schedule: On-site | Administrative Shift Shift Requirements: Must be available to work different shifts and/or weekends based on business needs Position Ava...
SUMMARY: Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies adva...
For validation services area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with two (2) years of experience as a Engineer within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skil...
Job Description: Under general supervision, this role provides engineering support across operations, manufacturing, pilot plant, and capital project environments. Responsibilities include process optimization, troubleshooting operational...
US - Puerto Rico - Juncos JOB ID: R- LOCATION: US - Puerto Rico - Juncos WORK LOCATION TYPE: On Site DATE POSTED: Sep. 14, **** CATEGORY: Maintenance Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of so...
mîrus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts ...
*Education:* -Doctorate + 2 years of Project Management experience OR -Masters + 4 years of Project Management experience OR-Bachelors + 6 years of Project Management experience OR -Associates + 10 years of Project Management experience...
The Sr Specialist, Quality Assurance serves as a technical expert supporting quality systems, validation activities, and compliance within a regulated manufacturing environment. This role is responsible for reviewing and approving product d...
*Education: * -Doctorate + 2 years of directly related experience OR -Masters + 4 years of directly related experience OR -Bachelors + 6 years of directly related experience OR -Associates + 10 years of directly related experience OR ...