Project Manager

For Project Manager services in the Manufacturing Engineering areas. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering and a minimum of seven (7) years of experience in Project Management activities within the Pharmaceutical or Medical Devices industry. Bilingual: Spanish and English Shift: Administrative & according to business needs Experience in: Developing and executing comprehensive project plans, including objectives, deliverables, schedules (using Gantt charts in MS Project), risk assessments, and resource allocation. Financial Management Regulatory requirements (e. g. , FDA, ISO)The Personality Part:

Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients and team members. In other words, being a customer service pro is one your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to take on this new challenge?AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)Project Planning: Develop a comprehensive project plan that outlines objectives, deliverables, timelines, and resource allocation.

Conduct risk assessments to identify potential challenges and develop mitigation strategiesBudget Management: Prepare and manage the project budget, ensuring accurate tracking of expenses versus planned costs. Implement cost-control measures to stay within financial targetsTeam Leadership: Assemble and lead a cross-functional team, including design, engineering, regulatory, quality assurance, and marketing professionals. Facilitate effective communication and collaboration among team membersStakeholder Engagement: Identify and manage key stakeholders, including internal teams, external partners, regulatory bodies, and customers. Keep stakeholders informed about project progress, challenges, and changesRegulatory Compliance: Ensure that the project adheres to relevant regulatory requirements and industry standards (e. g.

, FDA regulations, ISO standards). Coordinate with regulatory affairs teams to prepare submissions and maintain compliance throughout the project lifecycleQuality Assurance: Implement and oversee quality assurance processes to ensure the medical device meets all specifications and safety standards. Address any quality issues that arise during the projectSchedule Management: Create and maintain a detailed project schedule that tracks milestones, deadlines, and deliverables. Coordinate activities and manage dependencies to minimize delaysChange Management: Manage project scope and changes by evaluating requests and assessing their impact on timelines and budgets. Ensure proper documentation and approval processes are followed for any changesCommunication:

Provide regular updates to executive management and stakeholders regarding project status and key performance indicators. Facilitate meetings, workshops, and presentations to communicate project developmentsProblem Solving: Identify and address project-related issues promptly, employing problem-solving techniques to overcome obstacles. Foster an environment where team members feel comfortable raising concerns and proposing solutions Project Closure: Ensure proper project closure by conducting final evaluations, documenting lessons learned, and obtaining necessary approvals. Review project outcomes against initial objectives and provide reports to stakeholdersWHO WE ARE: We are a Service Provider company different from the rest.

We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the next piece?Powered by JazzHRLcGe9D2Ayg