Copy of Site Engineering Head

Posted Yesterday
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Hiring Remotely in Duvvada, Vishākhapatnam, Andhra Pradesh, IND
Remote
Expert/Leader
Pharmaceutical
We accelerate access to affordable and innovative medicines because Good Health Can’t Wait.
The Role
Lead manufacturing maintenance and reliability for a pharma site, ensuring equipment functionality, calibration, GMP compliance, zero downtime, preventive and breakdown maintenance, CAPEX/OPEX management, continuous improvement (LDM/TPM), audit readiness, and team development.
Summary Generated by Built In
Company Description

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.

We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.

For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).

‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency

Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.

"

Job Description

Job Summary

This role is for a Manufacturing Maintenance and Reliability Manager, responsible for ensuring the optimal functionality, calibration compliance, and reliability of manufacturing equipment across operations. The position drives zero downtime initiatives, leads preventive and breakdown maintenance programs, and manages the life cycle of critical assets through LDM, TPM, and continuous improvement strategies.

Key responsibilities include preparing CAPEX proposals, managing OPEX budgets, and executing projects within defined timelines and compliance frameworks. The role ensures adherence to GMP, safety standards, and validated process parameters, while promoting safety awareness and environmental compliance. It also involves managing QMS elements, audit readiness, and documentation practices.

" Roles & Responsibilities

  • Maintain manufacturing equipment to ensure correct functionality, calibration compliance, and operation within validated process parameters.
  • Develop and guide the team toward achieving zero downtime, higher equipment reliability, and maximum availability through proactive maintenance strategies.
  • Lead continuous improvement initiatives such as LDM, TPM, debottlenecking, and resource optimization, while leveraging cross-site learnings for enhanced productivity and cost efficiency.
  • Prepare CAPEX proposals, conduct feasibility studies, secure approvals, and ensure timely execution of projects in compliance with regulatory and business requirements.
  • Manage OPEX budgeting, tracking, and monitoring, along with developing and reviewing KPIs to drive operational efficiency and cost control.
  • Conduct breakdown analysis, improve preventive maintenance, and collaborate with cross-functional teams to resolve discrepancies and implement corrective actions.
  • Ensure compliance with GMP, safety standards, and SOPs, maintain audit readiness, and manage QMS elements including documentation, CAPA closure, and training.
  • Build a high-performing team by setting goals, conducting performance reviews, coaching employees, recognizing contributions, and driving capability development for seamless process engineering transitions.

"

Qualifications

Educational Qualification

Graduation in Instrumentation  Mechanical, Electrical, Engineering or related field is mandatory.
Post Graduation in Engineering / MBA is preferred.

Minimum Work Experience

20+years of experience in Pharma Industry.

Skills & Attributes Functional Skills

  • Asset Management
  • Commissioning Qualification Validation (CQV)
  • Total Cost of Ownership
  • Equipment Maintenance
  • Process Engineering
  • Project Management
  • Site Inspection
  • Sustainability Initiatives

Resident Skills

  • Audit Management
  • Current Good Manufacturing Practices (cGMPs)
  • Lean Methodologies
  • Risk Management
  • Total Productive Maintenance

Behavioural Skills

  • Accountability and ownership – takes full responsibility for equipment performance, team outcomes, and compliance standards.
  • Strategic thinking – anticipates operational challenges and drives long-term improvements through data-driven decisions and cross-functional collaboration.
  • People development focus – invests in coaching, recognition, and capability building to foster a motivated and skilled workforce.

Critical Exposures

  • 8+ years in Sterile engineering or plant maintenance roles, with 5+ years as team lead managing Mechanical / Electrical / HVAC / Instrumentation / Operations / Engineering Projects in pharma manufacturing is desired.
  • Experience in cGMP, EHS, regulatory compliance and audit readiness in pharmaceutical manufacturing is desired.
  • Experience with Computerized Maintenance Management System (CMMS), energy efficiency measures and sustainability initiatives for asset management is desired.
  • Exposure in budget preparation and monitoring for CapEx and OpEx aligned with engineering objectives is preferred.
  • Exposure to SCADA, BMS (Building Management Systems), and IoT-based predictive maintenance tools is preferred.

"

Additional Information

Benefits Offered

At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs.

The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.

" Our Work Culture

Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.

For more details, please visit our career website at https://careers.drreddys.com/#!/"

Skills Required

  • Bachelor's degree in Instrumentation, Mechanical, or Electrical Engineering
  • Post Graduation in Engineering or MBA
  • 20+ years of experience in the pharmaceutical industry
  • Asset management experience
  • Commissioning, Qualification and Validation (CQV) experience
  • Equipment maintenance expertise
  • Process engineering experience
  • Project management experience, including CAPEX proposal preparation and execution
  • Site inspection and sustainability initiative experience
  • Audit management and cGMP knowledge
  • Lean methodologies and risk management experience
  • Total Productive Maintenance (TPM) experience
  • 8+ years in sterile engineering or plant maintenance and 5+ years leading multi-discipline teams
  • Experience with CMMS (Computerized Maintenance Management System)
  • Exposure to SCADA, Building Management Systems (BMS), and IoT-based predictive maintenance tools
  • Experience with energy efficiency measures and sustainability for asset management
  • Experience with cGMP, EHS, regulatory compliance and audit readiness in pharmaceutical manufacturing
  • Exposure to budget preparation and monitoring for CapEx and OpEx
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The Company
HQ: Hyderābād
Year Founded: 1984

What We Do

We accelerate access to affordable and innovative medicines because Good Health Can’t Wait.

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