Our company holds a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. Mentor Technical Group 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 we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.

Job Description:

• Responsible for the development, creation, and revision of controlled documentation in accordance with client policies and procedures, current GMP, 21CFR820, ISO 1348.
• Establishes partnerships with managers and supervisors in production.
• Works with change control, quality investigations, CAPA team members, and other cross functional managers and supervisors and development engineers/teams to ensure that controlled documents being revised contain the correct information/parameters per process/product specifications.

Position Qualifications:

• University Degree – BA/BS – Bioscience, Business, Biology or science (preferred) Previous experience in medical device, biotech industries or pharmaceutical 3-5 years' experience in Technical Writing, in a GMP or medical device manufacturing 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.

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