Sr. CSV Specialist/ Lab Equipment Qualification

MENTOR Technical Group Corporation; Carolina (PR); On-site; USD 70,000 - 90,000; Full time

Job summary

MENTOR Technical Group Corporation is seeking an experienced professional in laboratory validation to join our team in Carolina, Puerto Rico. The ideal candidate will have a Bachelor’s degree in a relevant field and more than 5 years of experience with computerized systems validation in a manufacturing environment.

Key responsibilities include reviewing laboratory protocols, providing validation services, and ensuring compliance with regulatory requirements. Candidates must be bilingual in English and Spanish, with proficiency in project management tools.

Qualifications

• At least 3 years of experience with PLCs or laboratory instrumentation systems.
• Over 5 years of experience in validating laboratory computerized systems.
• Bilingual: English and Spanish.

Responsibilities

• Review and revise laboratory protocols and related documents.
• Provide CSV and SOP validation for laboratory equipment.
• Write validation and technical documentation.

Skills

LIMS

CSV (Computerized System Validation)

Laboratory Instrument Performance Qualification

Project Management

Technical Documentation

Regulatory Compliance

Education

BS in Chemistry, Biology, Microbiology, Computer Science, or related

Tools

MS Office

Visio

Job description

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, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.

Professional Summary

Experienced professional in laboratory protocol review, document revision, and validation of laboratory computerized systems (CSV) and SOPs. Skilled in LIMS and Empower, with extensive experience in laboratory instrument performance qualification and method configuration. Knowledgeable in regulatory compliance, data integrity, and project management within pharmaceutical manufacturing environments.

Professional Experience & Skills

Review and revise laboratory protocols and related documents.

Provide CSV (Computerized System Validation) and SOP validation services for laboratory equipment.

Experienced in LIMS and Empower platforms.

Laboratory instrument performance qualification, execution, and method configuration.

Familiar with GAMP5 methodology for validations.

At least 3 years of experience with PLCs, industrial computers, or laboratory instrumentation systems.

Strong understanding of network communication protocols (e.g., TCP/IP).

Proficient in project management tools and Visio.

Skilled in writing validation, commissioning, and technical documentation in English using MS Office applications.

Bilingual: English and Spanish.

Education & Qualifications

BS or higher in Chemistry, Biology, Microbiology, Computer Science, Information Systems, Engineering, or a related discipline.

More than 5 years of experience validating laboratory computerized systems in a manufacturing environment.

Trained in validation methodologies, technologies, and process control computer systems.

Strong knowledge of cGMP, FDA 21 CFR Part 11, and Data Integrity regulations.

Knowledgeable in computerized data collection systems and laboratory databases.

Background in pharmaceutical product manufacturing.

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.