ZipRecruiter

Log In

2

Remote Pharmaceutical Inspector Jobs in Chicago, IL

Danaher

Senior Engineer, Process Validation

Chicago, IL · On-site +1

$100K - $130K/yr

... remote. In this role, you will have the opportunity to: * Design, execute, and summarize ... Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing ...

Danaher

Senior Engineer, Process Validation

Chicago, IL · On-site +1

$100K - $130K/yr

... remote. In this role, you will have the opportunity to: * Design, execute, and summarize ... Knowledge of global regulatory requirements and cGMP regulations for pharmaceutical manufacturing ...

Tempus

Director, (GCP) Quality Assurance

Chicago, IL · On-site +1

Open to Hybrid in Chicago or Remote candidates Key Responsibilities & Core Ownership Champion ... Host and support company regulatory GCP inspections. * Oversee the clinical quality system document ...

All JobsPharmaceutical Inspector JobsRemote Pharmaceutical Inspector JobsRemote Pharmaceutical Inspector Jobs in Chicago, IL

Remote Pharmaceutical Inspector information

See Chicago, IL salary details

$12

$28

$53

How much do remote pharmaceutical inspector jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for remote pharmaceutical inspector in Chicago, IL is $28.18, according to ZipRecruiter salary data. Most workers in this role earn between $19.09 and $32.45 per hour, depending on experience, location, and employer.

What are the most commonly searched types of Pharmaceutical Inspector jobs in Chicago, IL?

The most popular types of Pharmaceutical Inspector jobs in Chicago, IL are:

What cities near Chicago, IL are hiring for Remote Pharmaceutical Inspector jobs?

Cities near Chicago, IL with the most Remote Pharmaceutical Inspector job openings:

Remote Pharmaceutical Inspector jobs near you

Sr. Quality Assurance Specialist

Sterling Engineering Inc.

North Chicago, IL • On-site, Remote

$40/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Job Title: Senior Quality Assurance Specialist | Pharmaceuticals
Location: North Chicago, IL
Hire Type: Long-term contract position (1 year +)
Pay Rate: $40.00/hour
Benefits: PTO, paid holidays, BCBS medical plans, dental/vision plans, 401(k), & ESOP
Work Schedule: Hybrid | Remote Monday & Friday; On-Site Tuesday–Thursday | 8:00 AM–5:00 PM
Travel: Up to 20%

Job Summary:
We are seeking a Senior Quality Assurance Specialist to provide Quality Assurance support for a pharmaceutical manufacturing project. This role will support a new project for a key product and ensure product, process, and system-related quality activities comply with applicable corporate and governmental regulations.
The Senior QA Specialist will lead and coordinate Quality projects across multiple site QA functions, manage project deliverables and metrics, identify and mitigate risks, and provide project updates to site management.

Must-Have Skills:
  • Quality Systems: Strong understanding of pharmaceutical Quality Systems and compliance requirements.
  • Communication: Excellent verbal and written communication skills with the ability to work across multiple QA functions.
  • Project Management: Experience planning, coordinating, and driving Quality projects from initiation through completion.
  • Aseptic Processing: Familiarity with aseptic manufacturing processes and associated quality requirements.
  • Combination Products: Experience or familiarity with combination product environments.
Job Duties:
  • Develop, coordinate, and drive execution of Quality projects across multiple site QA areas.
  • Coordinate with site QA planners to achieve project deliverables and timelines.
  • Support deployment of global pharmaceutical Quality initiatives across the site.
  • Analyze and maintain data related to cycle times, touch times, tasks, and processes to improve QA performance.
  • Support development and maintenance of QA planning and scheduling activities.
  • Implement and maintain visual management tools to monitor key QA processes and performance.
  • Analyze and report metrics for planned and unplanned QA activities.
  • Identify project and process risks and develop mitigation or contingency strategies.
  • Lead development of Project Charters, project objectives, requirements, and success criteria.
  • Support regulatory inspections related to new market introductions.
  • Lead or coordinate Compliance and Performance Improvement projects and provide project status updates to site management.
  • Maintain effective relationships with internal Quality functions and third-party contractors.
Qualifications:
  • Bachelor's degree in Science, Engineering, Quality, or a related field preferred.
  • Experience in pharmaceutical manufacturing, Quality Assurance, or a highly regulated environment.
  • Experience managing or coordinating cross-functional Quality projects.
  • Working knowledge of Quality Systems and regulatory compliance.
  • Familiarity with aseptic processing and/or combination products.
  • Strong analytical, organizational, and project management skills.
  • Excellent communication and interpersonal skills.
  • Ability to identify risks, develop mitigation strategies, and drive projects to completion.


Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.