GMP Facilities Mechanic; Onsite-Bridgewater, NJ

GMP Senior Facilities Mechanic

Pro Pharma has improved the health and wellness of patients by providing expertise.

This is a 4-month Contract role, 100% onsite.

Bridgewater, NJ Facility and associated equipment. This is a hands‑on position local to the Bridgewater, NJ facility.

• Perform routine maintenance and troubleshooting of process equipment in a cell therapy manufacturing facility in a 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 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.
• Manage parts, order, and coordinate with equipment vendors and area owners to schedule maintenance activities.
• Maintain tools and test equipment and ensure they are properly calibrated and in good 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.

• 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 prev enters is a plus).

• 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.

Pro Pharma celebrates its differences and strives to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion.