Oversee quality control in a GMP lab, ensuring compliance in pharmaceuticals/biotech. Requires bilingual communication, project management, and related experience in manufacturing and QA.
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:
- Laboratory experience in a GMP environment within the Pharmaceutical and/or Biotech industry
- Fully bilingual communications skills (English and Spanish)
- Good communications and presentation skills in English and Spanish
- Project management skills
- Strong organizational skills, including ability to follow assignments through to completion
- Enhanced skills in leading, influencing and negotiating
- Knowledge of and experience with processes involved in manufacturing and distribution, QA, QC, validation and process development
- Basic Knowledge and skills of word processing, presentations, and spreadsheet applications
Qualifications Requirements/Knowledge/Education/Skills:
- Ph.D OR MD + 2 years of directly related experience OR BS + 4 years of directly related experience OR Associates + 8 years of directly related experience OR High school/GED + 10 years of directly related experience.
- Educational background in Chemistry, Microbiology, Biology or Life Sciences
Top Skills
Gmp Environment
Presentations
Spreadsheets
Word Processing
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