Facilities Maintenance Technician (3rd Shift)

Fagron; Wichita (KS); In loco; USD 52.000 - 78.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive salary

Comprehensive benefits

Growth opportunities at international·

Dynamic team environment

Descrizione del lavoro

Fagron is seeking a Facilities Maintenance Technician to support sterile pharmaceutical production. The role emphasizes mechanical and electrical troubleshooting, preventive maintenance, and strict adherence to cGMP standards.

Expect hands-on work with CMMS, building systems, and cross‑functional collaboration with Quality and Engineering teams. Ideal candidates have 3+ years in regulated manufacturing, strong problem-solving skills, and the ability to read drawings and P&IDs.

Competenze

• High school diploma or equivalent; technical certification preferred.
• 3+ years in regulated manufacturing or pharmaceutical environments.
• Working knowledge of cGMP, FDA, and cleanroom standards.
• Experience with CMMS and maintenance planning.
• Ability to read drawings, P&IDs, and manuals.

Mansioni

• Repair and maintain plant equipment and building infrastructure per specifications, with cGMP adherence.
• Diagnose issues, replace parts, test, and adjust equipment.
• Understand electrical wiring and installation.
• Keep facility and equipment clean, safe, and serviceable.
• Interface with CMMS and manage spare parts inventory.
• Coordinate with Quality and follow change controls and work orders.
• Monitor Building Management System and environmental controls.
• Communicate status with internal teams and vendors; coordinate with sponsors.
• Support office and small equipment moves; perform related duties.

Conoscenze

Mechanical troubleshooting

Electrical troubleshooting

Reading technical drawings

Attention to detail

Team collaboration

Formazione

High school diploma

Technical certification in HVAC/maintenance

Strumenti

CMMS

Electrical testing equipment

Descrizione del lavoro

About the Job

Facilities Maintenance Technician plays a key role in maintaining and improving the reliability, safety, and efficiency of the facility and equipment supporting sterile pharmaceutical production at the Canton, MA facility. This role requires hands‑on technical skills, attention to detail, and strict adherence to cGMP (Current Good Manufacturing Practices) standards. The ideal candidate has experience in regulated manufacturing environments, a strong mechanical or electrical background, and a proactive approach to preventive and corrective maintenance.

Key Responsibilities

• Repair and maintain plant equipment and building infrastructure per manufacture specifications, SOP’s incompliance with cGMP’s
• Diagnose problems, replace, or repair parts, test and make appropriate adjustments
• Strong understanding of electrical wiring and installation
• Ensure facility and equipment are kept clean, in a safe, and serviceable condition
• Interface and augment Computerized Maintenance Management System (CMMS)
• Maintain spare parts inventory, order, and restock as required
• Partners with Quality and follows the necessary procedures (change controls, work orders, investigation, etc.) associated with building equipment and infrastructure
• Understands and monitors Building Management System (BMS) and coordination with Environmental Monitoring on temperature, relative humidity, and pressures issues.
• Communicates with internal departments, customers, and vendors on status of work and issues effecting services
• Coordinate tasks and scheduling with vendor resources
• Facilitate office and small equipment moves
• Performs other related duties as assigned

Basic Qualifications

• High school diploma or equivalent; technical or trade school certification in HVAC, electrical, mechanical, or industrial maintenance preferred.
• 3+ years of maintenance experience in a regulated manufacturing or pharmaceutical environment (503B, 503A, medical device, or biotech preferred).
• Working knowledge of cGMP, FDA, and cleanroom operational standards.
• Demonstrated experience with maintenance management systems (CMMS).
• Ability to read and interpret technical drawings, P&IDs, and equipment manuals.
• Strong troubleshooting skills across mechanical, electrical, pneumatic, and limited automation systems.
• Basic computer proficiency (Microsoft Outlook, Excel, Word).
• Reliable, detail-oriented, and able to work independently or as part of a team.
• Availability for occasional on‑call or weekend maintenance support.
• Attention to Detail – Maintains precise records and ensures work meets stringent regulatory and quality standards.
• Technical Aptitude – Demonstrates hands‑on expertise in troubleshooting and maintaining complex systems in a controlled environment.
• Problem Solving – Quickly identifies root causes of issues and develops effective corrective actions.
• Team Collaboration – Works effectively across departments, supporting production and engineering needs in a collaborative manner.
• Adaptability – Adjusts to changing priorities and requirements in a dynamic pharmaceutical manufacturing environment.
• Accountability – Takes ownership of assigned tasks and ensures timely, compliant completion.
• Safety Mindset – Promotes and practices a culture of safety and compliance in every aspect of work.

Physical Demands

The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully.

• Frequent standing, walking, bending, kneeling, stooping, crouching, crawling, and climbing throughout the day.
• The employee must be able to lift and/or move items over 50 pounds. Anything over 50 pounds will require a team lift.
• The specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.

The above statements describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.

What's on Offer?

We offer a dynamic environment where talent and ambition can develop to its fullest. We have an open and informal organization culture, where individuals need to have strong motivation and ability to work independently. Fagron is a widely expanding, international, professional and ambitious pharmaceutical company with multiple growth opportunities. Job opportunity includes competitive salary, comprehensive benefits, performance package, and ability to be part of an international leader in an expanding industry.

Ready for the challenge?

Fagron North America is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law.