Media Fill - Aseptic Engineer

Pfizer

Closes in 7 days

Quick summary

Work type
On-site
Location
Rocky Mount, NC
Salary
$82,700–$137,900 / yr
Posted
8 days ago
Closes
Jun 13, 2026 (soon)

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $169k
This role $110k
$68k most similar roles pay here $222k

This role pays less than 90% of similar roles. Most pay $130,500–$207,075 — the shaded band above. At the midpoint, this role pays about $110k versus about $169k for comparable roles.

Based on 240 similar postings.

Employer

About Pfizer

Pfizer Inc. is one of the world''s largest biopharmaceutical companies, researching, developing, manufacturing, and marketing medicines and vaccines across multiple therapeutic areas including oncology, cardiology, and infectious diseases. Industry: Biopharmaceuticals

Pfizer currently has 24 open roles on FindRole.

Listed pay typically runs $131,750–$219,650 across 24 roles with salary data.

Most-posted roles

View all roles at Pfizer

At a glance

TL;DR · Media Fill - Aseptic Engineer

As a Process Engineer at Pfizer, you will join a forward-thinking engineering team focused on accelerating the delivery of life-saving medicines. Your responsibilities include developing and refining process formulations to meet high-quality standards, recommending enhancements to solve complex problems, and ensuring compliance with FDA regulations and Good Manufacturing Practices. You will work in a structured environment using established procedures, coordinate project tasks, and support site compliance through equipment cleaning and documentation preparation. The ideal candidate has 2+ years of experience in manufacturing, proficiency in Microsoft applications, and knowledge of Drug Product processing and Lean Manufacturing principles. Strong interpersonal skills, attention to detail, and the ability to work effectively under pressure are essential. This role requires flexibility with schedules, including overtime and weekends, and occasional travel for equipment design reviews.

What you'll do

  • Develop and refine manufacturing processes to meet high-quality standards.
  • Recommend and implement process enhancements to solve complex problems.
  • Evaluate product requirements to determine optimal production costs and schedules.
  • Ensure compliance with FDA regulations, Good Manufacturing Practices, and SOPs.
  • Coordinate project activities, documentation, and outside resources for scheduled projects.

What we're looking for

  • Bachelor's degree with at least 2 years of experience or equivalent.
  • Demonstrated ability to solve complex problems in a manufacturing environment.
  • Working knowledge of FDA regulations and Good Manufacturing Practices (GMP).
  • Experience with Drug Product processing, equipment, process validation, and qualification.
  • Proficiency in Microsoft applications and familiarity with Lean Manufacturing principles.
  • Strong interpersonal skills, project management abilities, and team leadership experience.
  • Ability to work effectively under pressure, adapt to changing priorities, and manage complex information.

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