Associate Instrumentation Engineer

Pfizer

India

On-site

INR 700,000 - 1,100,000

Full time

2 days ago
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Job summary

Pfizer in India is seeking an Associate, Global Supply Engineering to help keep filling equipment and utility systems running reliably. You will plan preventive maintenance, manage work orders, and assist in installation, commissioning, and qualification of equipment.

You will contribute to process improvements, support capital projects to minimize life cycle costs, and ensure cGMP documentation. Strong written and verbal communication, teamwork, and problem-solving are essential for success in

Qualifications

  • Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience.
  • Experience in reliability-based maintenance practices
  • Demonstrated ability to write and provide simple and accurate instructions
  • Aseptic manufacturing experience
  • Demonstrated computer and technical skills
  • Effective problem-solving capabilities
  • Excellent interpersonal communication and written skills

Responsibilities

  • Support the Engineering team in planning and overseeing preventative maintenance for filling equipment.
  • Manage the status of work control and backlog from work order submission to completion.
  • Assist in maintenance work management and the installation, commissioning, and qualification of equipment.
  • Contribute to continuous process improvement initiatives.
  • Provide input on capital project design regarding equipment selection and specifications to minimize life cycle costs.
  • Communicate schedules to all resources, including maintenance, production, outside services, stores, and engineering.
  • Oversee pest control management in compliance with Good Manufacturing Practices (cGMP) and Pfizer internal requirements.
  • Manage and properly archive all utility documents and drawings.
  • Ensure the generation and maintenance of documentation supporting Good Manufacturing Practices (cGMP).
  • Contribute to project tasks and milestones, organize work to meet deadlines, and apply basic team effectiveness skills within the immediate Work Team.

Skills

Reliability-based maintenance
Written communication
Problem solving
Interpersonal communication

Education

Bachelor's degree
Associate's degree
High school diploma

Tools

CMMS
Microsoft Office

Job description

**Use Your Power for Purpose**Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you'll play a key role in accelerating the delivery of medicines to the world. Your innovative ideas and proactive actions will help us imagine new possibilities and bring them to life, making a significant impact on global health. As an Associate in the Global Supply division, you will contribute to improving patients' lives while working at Pfizer. Your dedication and expertise will ensure our plants, utility systems, buildings, and equipment are operational, helping us achieve new milestones and assist patients worldwide.**What You Will Achieve**In this role, you will:* Support the Engineering team in planning and overseeing preventative maintenance for filling equipment.* Manage the status of work control and backlog from work order submission to completion.* Assist in maintenance work management and the installation, commissioning, and qualification of equipment.* Contribute to continuous process improvement initiatives.* Provide input on capital project design regarding equipment selection and specifications to minimize life cycle costs.* Communicate schedules to all resources, including maintenance, production, outside services, stores, and engineering.* Oversee pest control management in compliance with Good Manufacturing Practices (cGMP) and Pfizer internal requirements.* Manage and properly archive all utility documents and drawings.* Ensure the generation and maintenance of documentation supporting Good Manufacturing Practices (cGMP).* Contribute to project tasks and milestones, organize work to meet deadlines, and apply basic team effectiveness skills within the immediate Work Team.**Here Is What You Need (Minimum Requirements)*** Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience* Experience in reliability-based maintenance practices* Demonstrated ability to write and provide simple and accurate instructions* Aseptic manufacturing experience* Demonstrated computer and technical skills* Effective problem-solving capabilities* Excellent interpersonal communication and written skills**Bonus Points If You Have (Preferred Requirements)*** Knowledge or experience working in a Good Manufacturing Practices (also cGMP) environment* Biopharma experience* Strong organizational skills* Ability to work independently and as part of a team* Proactive and self-motivated* Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance Work Location Assignment: On Premise
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