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Pharmaceutical Systems Manager Jobs (NOW HIRING)

Quality Systems Manager Work Location: Congers NY Improving Health through Science and Technology ... Pharmaceutical industries). Experience: โ€ข 5 years' experience in Quality in ISO certified and/or ...

Quality Systems Manager Work Location: Congers NY Improving Health through Science and Technology ... Biomedical or Pharmaceutical industries). Experience: 5 years' experience in Quality in ISO ...

Quality Systems Manager

Congers, NY ยท On-site

$125 - $150/hr

The primary mission of theQuality Systems Manager will provide strategic and tactical Quality ... Experience of regulatory inspections in Medical Devices or Pharmaceutical industries is a plus ...

Quality Systems Manager

Irvine, CA ยท On-site

$100 - $125/hr

The Quality Systems Manager ensures the Quality Management System (QMS) remains compliant ... pharmaceutical industry. * 2+ years of experience of people management experience, including ...

Quality Systems Manager

Irvine, CA ยท On-site

$100K - $145K/yr

The Quality Systems Manager ensures the Quality Management System (QMS) remains compliant ... pharmaceutical industry. * 2+ years of experience of people management experience, including ...

Quality Systems Manager

Irvine, CA ยท On-site

$100K - $145K/yr

The Quality Systems Manager ensures the Quality Management System (QMS) remains compliant ... pharmaceutical industry. * 2+ years of experience of people management experience, including ...

Quality Systems Manager

Irvine, CA ยท On-site

$100K - $145K/yr

The Quality Systems Manager ensures the Quality Management System (QMS) remains compliant ... pharmaceutical industry. * 2+ years of experience of people management experience, including ...

Quality Systems Manager

Schaumburg, IL ยท On-site

$110K - $129K/yr

BISCO is seeking a Quality Systems Manager to manage and maintain BISCO's Quality Management System ... Experience in a medical device, pharmaceutical, or regulated manufacturing environment. * Internal ...

Quality Systems Manager

Schaumburg, IL ยท On-site

$110K - $129K/yr

BISCO is seeking a Quality Systems Manager to manage and maintain BISCO's Quality Management System ... Experience in a medical device, pharmaceutical, or regulated manufacturing environment. * Internal ...

Momentous is seeking a Quality Systems Manager to help build, implement, and continuously improve a ... Working knowledge of dietary supplement, food, pharmaceutical, medical device, or a similarly ...

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Pharmaceutical Systems Manager information

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$46K

$102.1K

$153K

How much do pharmaceutical systems manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for pharmaceutical systems manager in the United States is $102,067.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $125,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Pharmaceutical Systems Manager jobs?

For Pharmaceutical Systems Manager jobs, the most frequently searched job titles are:

Infographic showing various Pharmaceutical Systems Manager job openings in the United States as of June 2026, with employment types broken down into 98% Full Time, 1% Part Time, and 1% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $102,067 per year, or $49.1 per hour.

Quality Systems Manager

North Chicago, IL โ€ข On-site

Contractor

Re-posted 14 days ago


Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Quality Systems Manager position. Please send me your updated resume if you have relevant experience and are interested in this opportunity.

Job Title : Quality Systems Manager
Location: North Chicago, IL
Duration: Long Term

Position Overview

We are seeking an experienced Quality Systems Manager to provide quality assurance support within a regulated pharmaceutical manufacturing environment. This role is responsible for ensuring compliance with corporate quality standards, FDA regulations, and industry requirements while driving supplier quality initiatives and strategic quality system improvements.

The ideal candidate will have strong experience in supplier quality management, quality systems, SAP, and quality agreements, with the ability to collaborate across cross-functional teams to support operational excellence and regulatory compliance.

Key Responsibilities

Prepare and maintain supplier quality scorecards and performance metrics.

Track, analyze, and trend supplier quality data to identify improvement opportunities.

Develop, review, and manage Supplier Quality Agreements.

Support Supplier Controls and supplier quality management activities.

Ensure compliance with GMP, FDA, corporate, and governmental quality standards throughout manufacturing operations.

Support quality functions including Document Control, Device QA, Labeling, Validation, Training, and Quality Intelligence.

Collaborate with Manufacturing, Validation, Regulatory Affairs, and cross-functional teams to achieve business objectives.

Utilize SAP and Quality Management Systems to support quality operations, reporting, and compliance activities.

Translate quality strategies into tactical execution while ensuring adherence to regulatory requirements.

Ensure product, process, and system quality activities from raw material inspection through final product shipment comply with corporate and governmental regulations.

Required Qualifications

Bachelor's Degree in Life Sciences or a related field.

8+ years of Quality experience within the pharmaceutical, medical device, biologics, cosmetics, combination products, or other regulated manufacturing industry.

Strong experience in Supplier Quality Management, Supplier Controls, and Quality Management Systems (QMS).

Experience preparing supplier scorecards and tracking/trending supplier quality performance.

Hands-on experience creating and managing Supplier Quality Agreements.

Working knowledge of SAP; experience with OneTrack/SolTRAQs and Veeva Vault is a plus.

ASQ Certification is preferred.

Experience supporting Document Control, Device QA, Labeling, Validation, Training, or Quality Intelligence functions is an advantage.

Strong understanding of GMP, FDA regulations, quality systems, and continuous improvement methodologies.

Excellent written and verbal communication skills.

Experience working in pharmaceutical or medical device manufacturing environments.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with your best contact number and the best time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/