Manufacturing Supervisor
Flexible & Integrated Technical Services, LLC
Guayama
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JOB DETAILS
SKILLS
Biotech and Pharmaceutical, Construction Engineering, Continuous Improvement, Corporate Policies, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Customer Support/Service, Documentation, English Language, Establish Priorities, FDA Requirements, Lean Six Sigma, Maintain Compliance, Manufacturing, Manufacturing Management, Medical Equipment, Metrics, Multilingual, Needs Assessment, People Management, Performance Analysis, Performance Reviews, Process Improvement, Production Control, Production Schedule, Production Support, Resource Management, Safety/Work Safety, Spanish Language, Standard Operating Procedures (SOP), Technical Operations, Time Management
LOCATION
Guayama
POSTED
14 days ago
For Supervising services
WHAT MAKES YOU A FIT: 
The Technical Part:
- Bachelor’s Degree in Management or related technical field preferred or and at least five (5) years of previous exposure as Manufacturing Supervisor within the regulated industry.
- Bilingual (Spanish and English)
- Shift: 3rd shift
- Experience in:
- Leading production staff.
- Planning, organizing, staffing, performance assessment, and ensuring compliance with corporate policies, SOPs, cGMP, and FDA regulations.
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)
- Lead and supervise assigned production staff, maintaining strong floor presence.
- Ensure compliance with corporate policies, plant SOPs, cGMP, FDA, and safety regulations.
- Plan and execute daily production schedules and communicate priorities across shifts.
- Review batch records and documentation to ensure accuracy and timely closure.
- Identify training needs and partner with trainers to ensure staff qualification.
- Coordinate with Quality, Technical Services, and Operations during investigations.
- Initiate and support deviation investigations, CAPA, and Manufacturing Incident Reports.
- Drive continuous improvement initiatives using LEAN and Six Sigma tools.
- Manage staffing, overtime, attendance, performance evaluations, and corrective actions.
- Monitor production metrics and support cost, quality, and safety improvements.
- Suspend production when operations do not meet acceptable parameters (Final Authority).
- Prioritize production schedules and allocate staff resources (Final Authority).
- Approve overtime and staffing adjustments to meet production demand.
- Participate with Quality and Technical teams in improvement initiatives (Shared Authority).
- 10–15 direct reports.
WHO 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?
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About the Company
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