Facilities Engineering Associate

Division Overview Aurolife Pharma’s North Carolina operations (under Aurobindo Pharma USA) play a key role in the company’s U.S. specialty and complex generics strategy, with Durham serving as a formulation and device‑focused R&D hub and Raleigh supporting commercial manufacturing. The NC sites primarily focus on respiratory and inhalation products such as metered‑dose inhalers, which are considered specialty drugs due to their complex drug‑device integration, along with dermatology products including prescription topical creams and ointments that require sophisticated formulation and bioequivalence approaches.

In addition, the Durham facility supports development of transdermal delivery systems, nasal sprays, and other complex dosage forms, positioning the NC footprint as a center for high‑barrier specialty products rather than conventional solid oral generics.

We are seeking a motivated Facility & Engineering Associate-I to support the operation, maintenance, and continuous improvement of facility systems and manufacturing equipment within a pharmaceutical production environment. The successful candidate will assist in maintaining utilities such as HVAC, water systems, compressed air systems, and cleanroom facilities while ensuring compliance with cGMP, safety, and regulatory requirements. Responsibilities include performing and tracking preventive maintenance activities, troubleshooting equipment issues, supporting equipment qualification, validation, and calibration activities, maintaining technical documentation, and collaborating with Production, Quality, Validation, and Engineering teams.

This role is a hands on role and will also involve scheduling and coordinating external vendors for calibration, maintenance, and service activities, as well as working closely with cross‑functional teams to plan and communicate schedules to minimize operational disruptions. This position is ideal for candidates with a degree in Mechanical, Electrical, or a related Engineering discipline who are eager to build a career in pharmaceutical manufacturing and facility engineering.

• Perform routine operation, monitoring, and maintenance of facility utilities, including HVAC systems, purified water systems, compressed air systems, boilers, chillers, and electrical equipment.
• Execute and track preventive and corrective maintenance activities on manufacturing and facility equipment to ensure reliable and compliant operations.
• Troubleshoot mechanical, electrical, instrumentation, and facility‑related issues and implement effective corrective actions.
• Support equipment qualification, commissioning, validation, calibration, and requalification activities in compliance with cGMP requirements.
• Schedule and coordinate external vendors for calibration, maintenance, and service activities while ensuring timely completion and minimal disruption to operations.
• Collaborate with Production, Quality Assurance, Validation, and Engineering teams to plan maintenance and calibration schedules and support manufacturing operations.
• Maintain accurate maintenance records, work orders, logbooks, asset information, and engineering documentation.
• Create, revise, and maintain Facility & Engineering department Standard Operating Procedures (SOPs), forms, and related documentation.
• Ensure compliance with cGMP, safety regulations, environmental standards, and pharmaceutical industry guidelines.
• Assist in facility improvement projects, equipment upgrades, energy‑saving initiatives, and continuous improvement programs.
• Participate in inspections, audits, investigations, and regulatory assessments related to facility, utility, and equipment systems.
• Follow established SOPs and contribute to maintaining a safe, efficient, and compliant work environment.
• Utilize engineering and maintenance software systems such as AutoCAD, PMMS, CMMS, DMS, Nicelon, QAMS, BMS, EMS and ERP systems to support daily operations, documentation, maintenance planning, and project activities.
• Expected to come on weekends and after hours in case of emergencies at the facility.

• Basic knowledge of cGMP regulations, FDA…