Validation Specialist

hace 2 días


San Juan, San Juan, Puerto Rico Mentor Technical Group A tiempo completo

Mentor Technical Group (MTG) 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, biotechnology, and medical device safety and efficacy guidelines.
With offices in Caguas, PR, Boston, MA & San Francisco, CA and we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.
Job Summary:  We are seeking a meticulous and experienced Validation Engineer specializing in Serialization to join our team.
The ideal candidate will be responsible for ensuring that serialization processes and systems meet industry standards and regulatory requirements.
This role involves designing validation test methods, conducting process validation studies, preparing detailed reports, and collaborating with cross-functional teams to ensure the integrity and quality of serialized products.
Key Responsibilities: Develop and execute validation protocols for serialization equipment, processes, and systems.
Document validation activities and results, maintaining comprehensive records for all validation activities.
Analyze validation test data to determine whether systems or processes meet validation criteria.
Ensure all serialization systems are running according to necessary specifications and comply with regulatory standards.
Collaborate with production staff to ensure operational consistency and effectiveness.
Coordinate with Quality Assurance and Engineering departments to ensure timely execution of validation activities.
Investigate and resolve issues that could impact product quality and serialization integrity.
Participate in quality audits and respond to audit findings with appropriate corrective actions.
Stay current with industry trends and regulatory standards to ensure validation processes are up-to-date.
Required Skills and Qualifications: Bachelor's degree in Engineering, Computer Science, or a related field.
Proven experience in validation engineering, specifically in serialization.
Strong knowledge of GMP regulations, validation protocols, and risk assessment methodologies.
Proficiency in validation tools and statistical analysis software.
Excellent problem-solving and decision-making skills.
Strong communication and collaboration abilities.
Attention to detail and a commitment to quality.
Preferred Qualifications: Master's degree in Engineering or a related field.
Certifications in validation practices or quality management systems.
Experience with regulatory audits and compliance.
Compensation and Benefits: Competitive salary based on experience.
Comprehensive benefits package including health, dental, and vision insurance.
Opportunities for professional development and career advancement.
Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.
Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
Powered by JazzHR



  • San Juan, San Juan, Puerto Rico Qrc Group Llc A tiempo completo

    At Qrc Group Llc, we are seeking a highly skilled Data Validation Specialist to join our team. This role will be responsible for performing validation activities on software and manufacturing equipment in the medical device industry.Skill Requirements:Computer system validation life cycleKnowledge and experience validating software and medical devices...


  • San Juan, San Juan, Puerto Rico Qrc Group Llc A tiempo completo

    Company OverviewThe Qrc Group Llc is a leading organization in the medical device industry, dedicated to providing innovative solutions and ensuring the highest standards of quality.Job SummaryWe are seeking a skilled CSV specialist to perform validation activities on software and manufacturing equipment. The ideal candidate will have a strong background in...


  • San Juan, San Juan, Puerto Rico Lumiere Systems A tiempo completo

    **Job Description**Lumiere Systems is seeking a highly skilled Validation Documentation Specialist to join our team. This role will be responsible for managing document trackers, creating FAT & SAT documentation, and supporting the execution of IQ, OQ & PQ testing.The ideal candidate will have strong written and verbal communication skills, as well as...


  • San Juan, San Juan, Puerto Rico Lumiere Systems A tiempo completo

    At Lumiere Systems, we are seeking an experienced Data Validation and Automation Specialist to lead the validation of major capital automation projects. This role requires a minimum of 5 years' experience in leading validation efforts for large-scale automation projects.Key Responsibilities:1. Validation and Compliance Knowledge: The ideal candidate will...


  • San Juan, San Juan, Puerto Rico Mentor Technical Group A tiempo completo

    Mentor Technical Group provides comprehensive technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering, we have the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines.Job Summary: We are seeking a meticulous and experienced...

  • Csv Specialist

    hace 4 semanas


    San Juan, San Juan, Puerto Rico Qrc Group, Llc A tiempo completo

    Job Description CSV specialist to perform validation activities on software and manufacturing equipment in a medical device industry.Skills: Computer system validation life cycle.Knowledge and experience validating software and medical devices equipment.Technical writing (English).Requirements Bachelor in Science 5 years of experience Experience in the...


  • San Juan, San Juan, Puerto Rico Mentor Technical Group A tiempo completo

    We are seeking an experienced validation specialist to join our team at Mentor Technical Group. Our company provides technical support and solutions for the FDA-regulated industry, ensuring compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines.Job Requirements:Bachelor's degree in Engineering, Computer Science, or a...


  • San Juan, San Juan, Puerto Rico Qrc Group Llc A tiempo completo

    Medical Devices Industry ExpertiseThe ideal candidate will have a strong background in the medical devices industry, with a minimum of 5 years of experience. They will also have a bachelor's degree in a relevant field, such as science or engineering.Computer System ValidationThe CSV specialist will be responsible for performing validation activities on...


  • San Juan, San Juan, Puerto Rico Qrc Group Llc A tiempo completo

    Job DescriptionThe CSV specialist will be responsible for performing validation activities on software and manufacturing equipment in the medical device industry. This includes developing and maintaining technical documentation, collaborating with cross-functional teams, and ensuring compliance with industry regulations.Skills RequiredComputer system...

  • Data Solutions Specialist

    hace 2 semanas


    San Juan, San Juan, Puerto Rico Mentor Technical Group A tiempo completo

    Mentor Technical Group (MTG) 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, biotechnology, and medical device safety and efficacy guidelines.With offices in...