Electrical Supervisor

About the role

The Project Lead - Electrical (Supervisor) position is open to local applicants only. It is not available for global assignments or for employees working outside of Cipla's U.S. subsidiaries or affiliates.

Responsibilities

• Design, review, and approve protocols for equipment and processes to produce pharmaceutical drug products meeting internal, external, and regulatory guidelines.
• Maintain the facility as per cGMP and regulatory requirements. Introduce new SOP’s, equipment, and instruments to improve the work environment by safety and quality points of view by working closely with Quality Assurance team.
• Compile and maintain records of validation documentation and electrical schematics, installed equipment, installation or operational problems, corrective, and preventive actions.
• Review the Design, Installation, Operational, and Product qualification of operations machinery.
• Project planning, design, monitoring, and project execution. Coordinate with project contractors for procurement and installation of projects work.
• Prepare and maintain revised layouts whenever modifications to the system are done for the plant or facility.
• Provide technical expertise for electrical infrastructure, control systems, and automation.
• Oversee installation, commissioning, and qualification of electrical systems including power distribution, PLCs, HMIs, and building management systems.
• Ensure electrical designs and installations comply with cGMP, FDA, NEC, and other regulatory standards.
• Modification / Changes of machine/process of the facility as per requirements.
• Prepare and maintain documentation to support internal and external audits.
• Ensure electrical engineering activities align with quality and regulatory requirements.
• Collaborate with Quality and Compliance teams to address audit findings and implement corrective actions.
• Work with Finance and Procurement teams to manage project budgets and capital expenditures.
• Review and approve vendor quotes, purchase orders, and invoices.
• Monitor financial performance and report variances to management.
• Prepare and submit Capital Expenditure (CapEx) requests with detailed scope, justification, and ROI analysis.
• Track approval status and ensure alignment with corporate financial planning.
• Support CapEx forecasting and reporting for electrical engineering initiatives.
• Ensure accurate and timely data entry and reporting within SAP modules relevant to electrical engineering and finance.
• Partner with Manufacturing, Quality Assurance, Validation, Regulatory Affairs, and external vendors.
• Facilitate effective communication and coordination across departments.
• Identify potential risks and implement mitigation strategies.
• Ensure electrical projects meet quality, safety, and environmental standards.
• To raise change controls, whenever required changes are to be made to facilities and equipment. Coordinate with other departments such as Civil, Mechanical, Admin, Quality Assurance, Production etc. for various day-to-day activities.
• Implementation of various projects pre-requirement.
• To maintain safety norms as per Health Safety & Environment guidelines.
• To monitor project activity for Unit IV, Scheduling, monitoring, and keeping track on CAPEX project activities. Detailing with respect to design, manufacture of tooling and methods, supervision of large onsite projects.
• Work closely with external electrical/instrumentation service agencies on upgrading existing systems and troubleshoot errors and breakdowns.
• Ensure all process improvement projects are completed on time and within budget. Diagnose, test, and analyze the performance of electrical components, assemblies, or systems.
• Troubleshoot the existing systems for any issues which hinder the operations in any manner.
• Ensure that the plant is maintained at all times for audit readiness.
• Perform any other job or responsibilities assigned by the reporting manager.
• Any other job allocated by the Department Head.

Requirements

• Bachelor’s degree in Engineering (Mechanical, Electrical, or related field); Master’s preferred.
• Minimum 5 years of experience in pharmaceutical or biotech engineering and validation project management.
• Strong knowledge of sterile manufacturing processes (vials, PFS, IV bags).
• Experience with validation lifecycle documentation and execution.
• Familiarity with project management tools (e.g., MS Project, Primavera).
• Experience with SAP systems for engineering and financial operations.
• PMP certification is a plus.
• Experience with audit preparation, financial oversight, and CapEx processes.
• Excellent communication, leadership, and problem-solving skills.

Qualifications

• Unassisted lifting up-to 10 kg, may be required.
• Standing/walking for 80% or greater than an 8-hour period.
• Usage of appropriate personal protective equipment when required.

Physical requirements

• Unassisted lifting up-to 10 kg, may be required.
• Standing/walking for 80% or greater than an 8-hour period.
• Usage of appropriate personal protective equipment when required.

Benefits

Not specified.

Schedule

General Shift: 8:30AM – 5:00PM (may vary based on business needs)

Pay

$76,000 - $103,000

Global Company Information

Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

About InvaGen Pharmaceuticals, a Cipla subsidiary

InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.

EEO Statement

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.