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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, 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.
Responsibilities:
- Supervising and leading multiple projects at the site
- Managing the project team and delegating tasks
- Ensuring project milestones are met on time
- Conducting team and planning meetings
- Liaising with executives and other departments and providing reports on project progress as required on a weekly basis
- Ensuring project timeline and budget are adhered to
- Managing project documentation
- Optimising processes and conducting team-building activities
Qualifications Requirements/Knowledge/Education/Skills:
- Bachelor's Degree in Engineering, Science or Business field and 8 years of experience.
- Knowledge in Pharmaceutical and Medical Devices.
- PMP Certification Preferred
- Fully Bilingual
- Over five (5) years of demonstrable experience in the pharmaceutical industry, preferably in the oral solid dosage operational environment
- Strong project management background within, for example, production, engineering, validation or quality; with a solid understanding of manufactured dosage forms
- MS Office and Microsoft Project knowledge and skills is a must.
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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