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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:
Perform assigned functions under direct supervision, ensuring accuracy and compliance with established procedures
Execute documentation-related activities according to project assignments, client requirements, and in compliance with cGMP and safety procedures
Provide technical support and guidance to ensure operational activities comply with corporate and regulatory policies in a cost-effective and timely manner
Prepare, review, and maintain all documentation required by the direct supervisor
Review and update Standard Operating Procedures (SOPs), Work Instructions (WIs), and forms to ensure compliance with regulatory standards
Ensure all work performed aligns with site objectives and meets client expectations and satisfaction
Support training and coaching of Mentor Technical Group personnel, when required, to ensure proper knowledge and effective performance of duties
Demonstrate strong customer-oriented behavior by understanding client needs, anticipating potential challenges, and communicating risks proactively
Ensure the quality of deliverables provided to clients by maintaining accuracy and compliance in all work products
Maintain professional relationships with MTG clients, fostering open communication, trust, and a high level of professionalism
Ensure high-quality service delivery by reviewing completed work, monitoring project status, incorporating client feedback, and verifying alignment with requirements
Maintain a proactive approach to identifying and supporting new business opportunities
Communicate issues to management promptly and provide recommendations for continuous improvement
Participate in identifying project opportunities by contributing technical expertise for both client and MTG benefit
Comply with MTG administrative requirements, including timesheets, CV updates, certifications, and attendance policies
Stay updated with current industry trends and regulatory changes applicable to validation and compliance within the pharmaceutical, biotechnology, food & beverage, cosmetics, and healthcare industries
Perform other duties as assigned by supervisor, management, or client
Bachelor’s degree in Engineering, Science, or a related technical field
Experience in regulated industries such as pharmaceutical, biotechnology, medical devices, or similar environments is preferred
Knowledge of cGMP, FDA regulations, and quality systems
Strong understanding of documentation practices including SOP revisions, work instructions, and technical reports
Ability to provide technical support and ensure compliance with corporate and regulatory requirements
Strong analytical, problem-solving, and organizational skills
Excellent written and verbal communication skills
Customer-focused mindset with the ability to build and maintain professional relationships
Ability to work effectively under supervision and within multidisciplinary teams
Proficiency in Microsoft Office and documentation management systems is a plus
Bilingual (English/Spanish) is preferred
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.
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Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Administrative
Industries
Internet Publishing
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