Kindeva Drug Delivery

Sr. Equipment Maintenance Technician

Kindeva Drug Delivery  •  Lexington, KY (Onsite)  •  2 days ago
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Job Description

Senior Maintenance and Calibration Technician Position
Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make:
If you are ready to work with purpose, join Kindeva Drug Delivery. As a Senior Equipment Maintenance Mechanic, you will play a critical role in ensuring the reliability, safety, and performance of manufacturing and utility systems within a pharmaceutical cGMP environment.
Your expertise will directly support the production of life-changing and life-saving prescription nasal spray medications by keeping complex utility and process equipment operating at peak performance. Through your technical leadership, troubleshooting skills, and regulatory focus, you will help minimize downtime, maintain compliance, and ensure every product is manufactured safely, efficiently, and on time.

Responsibilities:
Equipment, Utilities & Technical Leadership
• Serve as a Subject Matter Expert (SME) for at least one utility and/or process equipment system.
• Operate, monitor, and maintain utilities and production equipment supporting manufacturing and laboratory operations using Facility Monitoring Systems (FMS) and established SOPs.
• Perform scheduled preventive maintenance on utility and production equipment in a high-quality, timely, and safety-compliant manner to minimize downtime and ensure optimal operation.
• Perform corrective maintenance on utility and production equipment with a focus on root cause identification and long-term reliability.
• Troubleshoot and repair mechanical, electrical, pneumatic, and control system issues impacting manufacturing and utilities.
Equipment supported includes, but is not limited to:
◦ Utilities: HVAC systems, air compressors, boilers, Purified Water and Clean Steam skids
◦ Process Equipment: Formulation and filling equipment, assembly and packaging machines, autoclaves, environmental and stability chambers
Calibration & Vendor Management
• Perform maintenance tasks in classified areas, including clean rooms, while following gowning requirements.
• Ensure all work complies with internal policies, cGMPs, FDA, and other regulatory requirements.
• Identify and report out-of-tolerance conditions; initiate appropriate documentation and corrective actions.
• Manage vendor calibration activities, including scheduling, shipment coordination, return of equipment, review of vendor documentation, and hosting on-site service providers.

Safety, Compliance & Documentation
• Perform maintenance and calibration tasks in utility and classified areas, including cleanrooms, while following gowning and safety requirements.
• Maintain accurate, detailed records of maintenance, calibration activities, repairs, and spare parts usage.
• Complete calibration records and equipment logs in compliance with SOPs and industry regulations.
• Ensure all work complies with internal policies, cGMPs, FDA, and other regulatory requirements.
• Follow all workplace safety procedures and maintain a high level of safety compliance at all times.

Training, Communication & Operations Support
• Perform training tasks as assigned and within required timelines.
• Communicate effectively with stakeholders at all levels to ensure smooth shift-to-shift transitions and minimal disruption to operations.
• Respond to off-hour breakdowns and urgent maintenance needs on a rotating basis.
• Adhere to SOPs governing maintenance, calibration, and validation activities.

Qualifications:
Basic Qualifications:
• High school diploma or GED required; Associate’s degree or technical certification in mechanical, electrical, or industrial maintenance preferred.
• 7+ years of hands-on maintenance and calibration experience in a regulated manufacturing environment.
• 3+ years of experience in a pharmaceutical, biotech, or other highly regulated cGMP setting.
• Strong working knowledge of mechanical, electrical, pneumatic, and control systems.
• Proven troubleshooting and root-cause analysis skills.
• Ability to read and interpret technical drawings, manuals, and specifications.
• Strong documentation, communication, and interpersonal skills.
• Ability to read and interpret technical drawings, manuals, and calibration specifications.
• Excellent communication and interpersonal skills.
• Ability to work in varying environments, including clean rooms, production areas, and laboratories.

Preferred Skills:
• Experience with device manufacturing and equipment processes.
• Experience with PLC (Programmed Logic Controller) troubleshooting, programing and wiring.
• Strong understanding of cGMP regulations, FDA requirements, and other relevant industry standards.
• Previous experience with manufacturing and maintenance software and systems (e.g., CMMS, ERP, MES, SCADA, OSI PI)

Physical Requirements:
• Regular use of hands for documentation, equipment operation, and material handling
• Extended periods of standing and walking
• Ability to lift/move
• Full range of vision capabilities (close, distance, color, peripheral, depth)
• Must wear required PPE and follow cGMP/safety procedures
• Lift heavy equipment to 60 pounds occasionally, climb ladders, and work in confined spaces.

# LI-Onsite

California residents should review our Notice for California Employees and Applicants before applying.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Equal Opportunity Employer:

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

Do you see yourself as part of the Kindeva mission? Click Apply Now Today!
Kindeva Drug Delivery

About Kindeva Drug Delivery

Kindeva is a purpose-fueled, people-centric CDMO dedicated to advancing your project, your ambitions, and our industry. With a legacy of innovation and deep expertise in complex drug development, we serve as a trusted partner to pharmaceutical companies worldwide.

For us, fast-tracking healthier tomorrows starts with industry-leading finished-dose expertise. From early-stage formulation to full-scale commercial production, we optimize every step to help bring life-changing therapies to patients faster.

Built on a rich heritage of regulatory diligence and blockbuster devices, our expertise sharpens, optimizes, and maximizes your project—combining best-in-class facilities with specialist capabilities in injectable, inhalation, and dermal delivery, to ensure exceptional-by-design solutions throughout.

Strategically minded and dedicated to your lasting legacy, we provide value beyond manufacturing, turning your long-term possibilities into achievable milestones.

Because every patient deserves tomorrow.

For more information about how we can transform tomorrows together, please visit www.kindevadd.com.

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Woodbury, Minnesota
Year Founded
2020
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