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1. C&Q Strategy & Planning • Develop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements. • Define system boundaries and identify direct/indirect impact systems. • Lead risk assessments (e.g., ISPE Baseline, ASTM E2500) to det

BioPharma Consulting JAD Group

The Senior Process & Systems Engineer independently leads and directs process optimization initiatives and the troubleshooting of operational issues across manufacturing, operations, pilot plant, and capital project environments. This role applies advanced and diverse engineering principles to d

Mentor Technical Group

Mentor Technical Group (MTG) provides technical support and solutions for the FDA-regulated life sciences industry. With offices in Caguas, Puerto Rico, and Boston, United States, we serve clients in six global markets, including the United States, Puerto Rico, Dominican Republic, Mexico, Germany, C

CIS International LLC

SUMMARY: Perform one or more of the following duties and responsibilities in support of Amgen's Quality Assurance program under minimal supervision. FUNCTIONS: Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident tr

Validation & Engineering Group, Inc.

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management,

FITS, LLC

For Manufacturing Services in the Quality Systems a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with five (5) years of experience as a Scientist within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skills. Shift: Administrative a

Company Description QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website http://www. qrcgroup.com / to learn more about our services and solutions! Job Description The Sr

MiniMed

At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate world. About The Role Are you a

Inteldot

Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico . Administrative Shift Job Description: Independently provides and/or directs the characterization o

FITS, LLC

For Quality services in the Manufacturing/Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering or Life Sciences and at least five (5) years of experience in Quality activities within the medical device industry. Bilingual (English & Spanish). Shift: Admini

Specific responsibilities include but are not limited to: • Own change controls for manufacturin g process changes • Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation, determination of Corrective/Preventive Actions, authoring proc

Quality Consulting Group, LLC

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 enthusiastic team, contributing in a world-class manufacturing indust

MiniMed

At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate world. About The Role At MiniMed

Must Experience in Regulated Industry Proficient in creating and executing validation and qualification documentation Provide support to vision inspection qualification and characterizations Plus A Plus: Knowledge in automated vision inspection systems A Plus: Knowledgeable in CSV. Support CQV docum

Amgen

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s

Quality Consulting Group, LLC

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 enthusiastic team, contributing in a world-class manufacturing indust

Cedrela Talent

Summary of Role: Oversee, manage and coordinate all operational aspects of projects impacting multiple departments. Responsibilities: Manage all aspects of project(s): planning, implementation, monitoring, completion, and follow-up. Manage competing timelines and prioritize critical tasks. Establish

Infotree Global Solutions

SUMMARY What attributes (i.e. - preferred qualifications) would make this candidate stand out? • Relevant experience in a commercial biopharmaceutical manufacturing environment, preferably supporting formulation and aseptic filling operations. • Understanding of protein science, formulation and fill

FITS, LLC

For Scientist Services in the Process Development: Inspection Projects a rea. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with four (4) years of experience as a Scientist within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skills. Sh

ProQuality Network

Tittle: Manufacturing Specialist (35380) Location: Juncos, Puerto Rico (Open to Puerto Rico Residents) Work Schedule: On-Site | Administrative Shift Contract Duration: 5 Months Position Summary We are seeking a Manufacturing Specialist to support manufacturing and quality operations within a regulat