Quality Specialist - Juncos

Nos encontramos en la búsqueda de un/a Quality Specialist para un proyecto en el área Sur de Puerto Rico, dentro de la industria de Medical Devices. · ...

We're seeking a Specialist QA to work for one of our top Biotechnology Industry clients at Juncos, PR. · Review and approve product MPs. · Approve process validation protocols and reports for manufacturing processes. · ...

Perform one or more of the following duties and responsibilities in support of Quality Assurance program under minimal supervision. · ...

Mentor Technical Group provides technical support and solutions for the FDA-regulated industry. · ...

We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you. We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US ...

We are a Service Provider company different from the rest. We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well). Our company is flexible, family-oriented and focused on our resources' well-bein ...

Mentor Technical Group provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. We serve life sciences clients in six global markets. · ...

The Quality Assurance Specialist performs various duties in support of quality assurance programs under minimal supervision. · Doctorate OR Masters + 2 years of directly related experience OR Bachelors + 4 years of directly related experience OR Associates + 8 years of directly r ...

We are a Service Provider company looking for a Quality Specialist to join our team. The ideal candidate will have a Bachelor's Degree in a related field and four years of experience in the pharmaceutical or regulated industry. · ...

+ Mentor Technical Group provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, bio ...

Supports equipment and test method validation and supporting documentation as an author or quality reviewer. Supports process documentation changes as author or quality reviewer. Provides oversight of quality processes and procedures that ensure compliance with policies and the p ...

Lead and execute Computer System Validation (CSV) activities for Quality Information Technology systems in compliance with FDA, GxP, ISO, and global regulatory requirements. · Conduct and maintain formal validation documentation, including Validation Plans, Risk Assessments, IQ, ...

We are seeking a talented, · d · dicated individual committed to work under the highest ethics standards for the following position: · QA SpecialistThe QA Specialist ensures compliance with quality systems,overses batch record reviews,and supports the implementation of new produc ...

We are seeking a talented individual committed to work under the highest ethics standards for the following position: Quality Assurance Specialist.The QA Specialist plays a critical role in ensuring that all biotechnology and pharmaceutical products meet regulatory standards and ...

Validation & Engineering Group, Inc. (V&EG) 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, Valid ...

We are looking for a talented and highly motivated Sr Quality Systems Specialist to join our team in Puerto Rico & USA. · ...

A leader in the pharmaceutical industry is looking for a motivated and enthusiastic team member to join their team. · ...

We are seeking an Associate Quality Application Specialist who will conduct compliant validation processes for quality information technology systems. · ...

This role involves working with a highly enthusiastic team in the manufacturing industry in Puerto Rico and USA. · Conducts a compliant validation process for quality information technology systems under appropriate federal regulations. · Coordinates activities with clients, prog ...

Job summary:For Engineer services in the Quality area.Responsibilities:Provides oversight for the development and maintenance of quality programs, ...