Facilities Manager(GMP)

.GMP certification/experience is mandatory.

Job Summary:

. Manage the day-to-day operations of pharmaceutical manufacturing, laboratory, warehouse, and office facilities to ensure a safe, compliant, and efficient working environment.

. Ensure facilities operations are conducted in compliance with regulatory requirements, including Good Manufacturing Practice (GMP), Good Distribution Practice (GDP)where applicable, and company Quality Management Systems.

. Lead site facilities teams and contractors to maintain critical building systems such as HVAC, cleanrooms, utilities, water systems, electrical, fire protection, and building infrastructure.

. Partner closely with Quality Assurance, Engineering, EHS, Validation, Production, and other stakeholders to support uninterrupted pharmaceutical operations.

. Ensure all facilities-related activities, maintenance programs, documentation, and change controls comply with GMP standards and audit requirements.

. Support internal, customer, and regulatory inspections and ensure timely closure of observations and corrective actions.

. Drive continuous improvement initiatives to enhance compliance, operational reliability, safety, and cost efficiency.

Key Responsibilities:

. GMP & Regulatory Compliance

. Ensure all facility operations and maintenance activities are performed in accordance with GMP requirements and site quality procedures.

. Maintain facility documentation, SOPs, maintenance records, calibration records, and logbooks in compliance with GMP standards.

. Participate in investigations, deviation management, CAPA implementation, change control, and risk assessments related to facilities systems.

. Support regulatory inspections, customer audits, and quality audits.

. Ensure contractors working within GMP areas comply with site quality, safety, and contamination control requirements.

. Critical Utilities & Infrastructure Management

. Oversee operation and maintenance of:

HVAC and cleanroom systems

Building Management Systems (BMS)

Electrical distribution systems

Compressed air systems

Water systems (Purified Water, WFI where applicable)

Critical process utilities

Fire protection systems

Emergency power systems

. Monitor facility performance and ensure compliance with environmental and cleanroom parameters.

. Quality & Risk Management

. Work closely with QA to ensure facility systems remain in a validated state.

. Support qualification and validation activities for facilities and utilities.

. Conduct routine facility inspections and audits to identify compliance gaps.

Ensure timely execution of preventive maintenance programs to minimize operational risks

Knowledge, Skill and Abilities Required:

. Bachelors degree in engineering, engineering technology.

. Minimum 5-8 years of Facilities Management experience within a pharmaceutical, biotechnology, medical device, life sciences, or regulated manufacturing environment.

. Proven experience managing facilities within a GMP-regulated environment is mandatory.

. Experience supporting pharmaceutical manufacturing facilities, laboratories, cleanrooms, and critical utilities.

. Experience handling regulatory inspections, audits, and compliance programs.

. Strong interpersonal relations ability, excellent oral and written communications skills

. Excellent time management and teamwork skills