ENGINEERING AND QUALITY PROFESSIONALS (MULTIPLE POSITIONS) @ EQVAL GROUP
EQVAL Group is currently expanding and seeking talented professionals to join our growing team across various locations in Puerto Rico. We are looking for individuals who are passionate about excellence in the engineering and manufacturing sectors, specifically within the pharmaceutical and medical device industries. As part of our team, you will have the opportunity to contribute to high-impact projects that ensure product quality and regulatory compliance across diverse production environments.
Candidates should possess a strong technical background and a commitment to professional growth within the life sciences sector. We offer a dynamic work environment where innovation and collaboration are valued. If you are ready to take the next step in your career and work with a dedicated group of experts, we encourage you to join our growing organization. Positions may be available at various sites throughout the island, supporting our mission to provide top-tier validation and quality services to our global clients.
Candidates should possess a strong technical background and a commitment to professional growth within the life sciences sector. We offer a dynamic work environment where innovation and collaboration are valued. If you are ready to take the next step in your career and work with a dedicated group of experts, we encourage you to join our growing organization. Positions may be available at various sites throughout the island, supporting our mission to provide top-tier validation and quality services to our global clients.
Key Requirements
Bachelor’s degree in Engineering, Science, or a related technical field.
Proven experience in the pharmaceutical or medical device manufacturing industry.
Proficiency in quality assurance and validation protocols (IQ/OQ/PQ).
Strong analytical and problem-solving skills for complex technical issues.
Ability to work effectively in a team-oriented and collaborative environment.
Excellent communication skills, both written and verbal in English and Spanish.
Deep knowledge of cGMP (Current Good Manufacturing Practice) regulations.
Proficiency in technical writing and documentation for regulatory submission.
Ability to manage multiple projects and meet strict deadlines.
Experience with process improvement methodologies and manufacturing technologies.