What are the responsibilities and job description for the Facilities Maintenance Engineer position at Cellares?
We are seeking an innovative and highly motivated GMP Facilities Engineer who will contribute significantly to the success of service maintenance, repair, and supporting the Cellares Bridgewater, NJ Facility and associated equipment.This position's primary focus will be performing preventative maintenance, repairs, calibration, and troubleshooting of GMP process equipment and Cellares Utility and Facility equipment. It is a hands-on position 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.ResponsibilitiesPerform routine maintenance and troubleshooting of Cellares and other process equipment in a cell therapy manufacturing facility in a Good Manufacturing Practice (GMP) environmentCollaborate with cross-functional teams to ensure compliance with GMP standards and regulationsPerform equipment calibrations and support validation testing to meet quality and regulatory requirementsRespond promptly to equipment failures and implement corrective actions to minimize downtime. Provide on-call support as requiredExecute preventative maintenance activities to ensure optimal functionality of manufacturing equipmentSupport installing and qualifying new equipment, ensuring adherence to GMP guidelinesSupport facilities team in providing maintenance and repair in the GMP environment as neededMaintain 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 SystemsManage parts, order, and coordinate with equipment vendors and area owners to schedule maintenance activitiesMaintain tools and test equipment and ensure they are properly calibrated and in good safe working conditionCollaborate with manufacturing and quality control teams to address technical issues and optimize processesSupport Quality Change Controls and CAPA investigationsStay updated on industry trends and advancements to contribute to continuous improvement initiativesParticipate in training programs to enhance technical skills and knowledgeAdditional Equipment Experience : Experience with HVAC, RTUs, Split Systems, LP Boilers, Air Compressors / dryers, Process Gas Distribution, Process Lab equipment (BSCs, Incubators, FZRs, REFs, Cryo Storage, Centrifuges, Pumps, Vacuum Skids, and backflow preventers is a plusRequirementsAssociate 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 biopharmaceuticalsStrong understanding of GMP regulations and quality standardsProficient in troubleshooting and repairing complex manufacturing equipmentAbility to read and understand technical documents and engineering drawingsExcellent organizational and documentation skillsAbility to work collaboratively in a team-oriented environmentEffective communication skills to interact with diverse stakeholdersDetail Oriented with a commitment to maintaining high-quality standardsAbility to lift and carry up to 50 lbs$90,000 - $210,000 a yearCellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.
Salary : $210,000
