Sr. C&Q Specialist

Mentor Technical Group; Juncos (PR); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading global life sciences consulting firm located in Juncos, Puerto Rico, seeks a professional to develop and maintain commissioning and qualification procedures. The ideal candidate will hold a Bachelor's or Master's degree in Chemical Engineering or Pharmaceutical Technology and have at least 2 years of GMP manufacturing experience. Fluency in English and strong analytical, problem-solving, and communication skills are essential. Join a collaborative team to ensure compliance and enhance quality in the pharmaceutical industry.

Qualifications

• Minimum 2 years of experience in GMP manufacturing.
• Strong understanding of regulatory requirements and quality standards.
• Proficiency in English; additional language skills are a plus.

Responsibilities

• Collaborate with C&Q Engineers to develop and maintain procedures.
• Write, review, and approve C&Q protocols and reports.
• Execute commissioning and qualification activities.

Skills

Collaborative teamwork

Analytical skills

Problem-solving

Regulatory knowledge

Communication skills

Education

Bachelor's or Master's in Chemical Engineering or Pharmaceutical Technology

Job description

Overview

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.

Responsibilities

• Collaborate with C&Q Engineers to develop and maintain commissioning and qualification procedures and documents.
• Write, review, and approve C&Q protocols and reports for various systems (e.g., HVAC, utilities, production equipment, lab equipment).
• Execute commissioning and qualification activities for plants and equipment.
• Coordinate with external consultants and internal resources to ensure timely document generation and execution.
• Manage change controls and deviations related to plants and equipment.
• Support maintenance and calibration functions to improve compliance and quality.
• Provide expertise in troubleshooting and root cause investigations.
• Facilitate the transfer of technical knowledge across units and sites.

Qualifications

• Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Technology, or a related scientific field.
• At least 2 years of experience in GMP manufacturing relevant to the area of expertise.
• Proficiency in English; additional language skills are a plus.
• Strong understanding of regulatory requirements and quality standards.
• Excellent analytical, problem-solving, and communication skills.
• Ability to work collaboratively in a team environment.

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.