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Quality Systems Writer Jobs (NOW HIRING)

Quality Systems Engineer

Devens, MA ยท On-site

$75K - $103K/yr

This position is responsible for writing and updating QMS procedures and is accountable for ... Ensure that a Quality System is established and maintained to the highest levels of accordance with ...

Quality Systems Specialist

Leesburg, VA ยท On-site

$80 - $100/hr

Quality Systems Specialist Location: Leesburg, VA (Preferred) or Allendale, NJ (Hybrid) (10% Travel ... Strong interpersonal, written, and oral communication skills with the ability to influence and ...

... Write and revise SOPs, controlled forms, and related documents to ensure best practices and alignment with current operations. โ€ข Develop Quality Systems team members to optimize performance and ...

We're currently hiring for the role of Quality Systems Manager at our Georgia facility. Additional ... Including PFMEA, Control Plan, Process Flow Chart and drawings (GD&T). 4. Strong oral and written ...

About our role We have an exciting opportunity for a Quality Systems Technologist to join our ... Strong written and verbal communication skills, with the ability to simplify complex information ...

Quality Systems Specialist The Quality Systems Specialist manages quality control (QC) analytical ... Strong verbal, written, and interpersonal communication skills to collaborate effectively with ...

We are looking to hire a Quality Systems Manager at our Gretna, LA plant. What We Bring To The ... and written communication skills necessary. Communication with upper management, regulatory ...

Quality Systems Manager

Congers, NY ยท On-site

$125 - $150/hr

Write and revise SOPs, controlled forms, and related documents to ensure best practices and alignment with current operations. * Develop Quality Systems team members to optimize performance and ...

Quality Systems Engineer

Hudson, NH ยท On-site

$100 - $125/hr

The Quality Systems Engineer is responsible for developing, implementing, maintaining, and ... Excellent written and verbal communication skills. * Ability to execute complex projects, and self ...

New

Quality Systems Analyst

Boston, MA ยท On-site

$120 - $125/hr

Strong written and verbal skills. * Ability to communicate across various cross-functional teams ... Strong computer skills - Word, Excel, and other electronic Quality systems. Responsibilities ...

Showing results 21-40

Quality Systems Writer information

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How much do quality systems writer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality systems writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

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Infographic showing various Quality Systems Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $81,001 per year, or $38.9 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/