Facilities Maintenance Engineer
Bridgewater, NJ
Facilities & Supply Chain - Facilities /
Full Time /
On-site
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Position Summary
We are seeking an innovative and highly motivated Facilities Maintenance Engineer who will contribute significantly to maintenance, repair, and support for equipment at the Cellares Bridgewater, NJ facility.
The primary focus of this position will be to perform preventive maintenance, repairs, calibration, and troubleshooting of GMP process equipment, along with Cellares Utility and Facility equipment. This is a hands-on position that is local to the Bridgewater, NJ facility.
Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle challenges as the company grows.
Responsibilities
Perform routine maintenance and troubleshooting of Cellares and other process equipment in a cell therapy manufacturing facility in a Good Manufacturing Practice (GMP) environment
Collaborate with cross-functional teams to ensure compliance with GMP standards and regulations
Perform equipment calibrations and support validation testing to meet quality and regulatory requirements
Respond promptly to equipment failures and implement corrective actions to minimize downtime. Provide on-call support as required
Execute preventative maintenance activities to ensure optimal functionality of manufacturing equipment
Support installing and qualifying new equipment, ensuring adherence to GMP guidelines
Support the facilities team in providing maintenance and repair in the GMP environment as needed
Maintain accurate documentation of all maintenance activities and equipment logs in a Computerized Maintenance Management System (CMMS)
Execute alarm response and proficiency in Building Maintenance Systems and Environmental Monitoring Systems
Order, coordinate, and schedule maintenance activities with equipment vendors and area owners
Maintain tools and test equipment to ensure they are calibrated and in safe working condition
Collaborate with manufacturing and quality control teams to address technical issues and optimize processes.
Support Quality Change Controls and CAPA investigations
Stay updated on industry trends and advancements to contribute to continuous improvement initiatives
Participate in training programs to enhance technical skills and knowledge
Additional Equipment Experience:
Requirements
Associate degree or equivalent in engineering or a related field with five plus years of experience in a GMP manufacturing environment, preferably in cell therapy or biopharmaceuticals
Strong understanding of GMP regulations and quality standards
Proficient in troubleshooting and repairing complex manufacturing equipment
Ability to read and understand technical documents and engineering drawings
Excellent organizational and documentation skills
Ability to work collaboratively in a team-oriented environment
Effective communication skills to interact with diverse stakeholders
Detail-oriented with a commitment to maintaining high-quality standards
Ability to lift and carry up to 50 lbs
$90,000 - $210,000 a year
Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.
This is Cellares
Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company's Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares' Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.
Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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