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Associate Instrumentation Engineer

Pfizer
Visakhapatnam, IND
Full-time
Associate
Onsite
Discovered 3 weeks ago
reliability-based maintenanceaseptic manufacturingpreventative maintenance planningequipment installation and commissioningequipment qualificationcGMP

Full Job Posting

Role Overview

Engineering is crucial to ensuring customers and patients receive medicines precisely when needed.

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 plants, utility systems, buildings, and equipment are operational.

What You Will Achieve

  • 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.

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.

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 productivity.

Work Location

  • Work Location Assignment: On Premise.

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