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Quality Systems Writer Jobs (NOW HIRING)

onsemi

Quality Systems Engineer

Hudson, NH · On-site

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

Marvin Group

MANAGER, QUALITY SYSTEMS

Inglewood, CA

As the Manager of Quality Systems, you will be expected to manage and lead the organizational ... Strong written and verbal communication, organizational and computer skills. (Required) * Ability ...

Astrix Inc

Quality Systems Specialist

Florence, KY · On-site

$25 - $28/hr

Pay Rate Low: 25 | Pay Rate High: 28 Quality Systems Specialist Location: Florence, KY Job Type ... Excellent written and verbal communication skills. * Ability to communicate effectively with ...

Delta Research

Quality Systems Manager

Livonia, MI

... written submission or other immigration support from the company (e.g., H-1 B, OPT, STEM OPT, CPT ... Quality Systems Manager POSITION SUMMARY Reporting directly to the VP of Quality with ...

Trystar Inc

Quality Systems Specialist

Burnsville, MN · On-site

$70K - $80K/yr

Job Title: Quality Systems Specialist Trystar is a leader in power distribution equipment and ... Strong written and verbal communication skills. Preferred Qualifications * Internal Auditor ...

Marvin Group

MANAGER, QUALITY SYSTEMS

Inglewood, CA · On-site

As the Manager of Quality Systems, you will be expected to manage and lead the organizational ... Strong written and verbal communication, organizational and computer skills. (Required) * Ability ...

Gentuity

Quality Systems Manager

Sudbury, MA · On-site

Excellent verbal, written and presentation skills * Detailed organization skills * Team player with excellent communication skills * ISO 13485 and FDA Quality System Regulation * Strong knowledge of ...

Stratasys Ltd

Manager, Quality Systems

Belton, TX · On-site

$100 - $125/hr

Manager, Quality Systems Location: Belton, TX, US Job ID: 55440 Category: Manufacturing ... Excellent written & verbal skills including the ability to read and write specifications ...

Gentuity LLC

Quality Systems Manager

Sudbury, MA · On-site

$145K - $165K/yr

... written and presentation skills • Detailed organization skills • Team player with excellent ... Quality System Regulation • Strong knowledge of Quality Systems programs including but not ...

PFNonwovens LLC

Quality Systems Engineer

Hazleton, PA · On-site

Strong written and verbal communication skills. * Demonstrated technical, business, and leadership skills. * Knowledge of quality systems (ISO, EDANA, and/or GMP). * Skilled in statistics, problem ...

Gentuity

Quality Systems Manager

Sudbury, MA

Internal and External auditing Corrective and Preventive action Excellent verbal, written and ... FDA Quality System Regulation Strong knowledge of Quality Systems programs including but not ...

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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.

Specialist, Quality Systems

Tustin, CA • On-site

Avid Bioservices
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Avid Bioservicesexternal

$31.63 - $42.16/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 days ago

Job description

Description
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
Join our team as a Specialist, Quality Systems, where you will play a vital role in ensuring the integrity and compliance of our Quality Management System. Provide support within Quality Systems for the processing of Discrepancy reports and CAPA records, ensuring adherence to procedural and regulatory requirements. Collaborate with cross-functional teams, maintain inspection readiness, and provide exceptional support to internal and external customers. If you thrive in a fast-paced environment and are dedicated to delivering top-notch quality, apply now to contribute to our organization's success.
Key Responsibilities:
  • Update existing channels for tracking Quality Event deviation reports and CAPAs.
  • Work with cross-functional teams to maintain adherence to task due dates.
  • Interact with interdepartmental contacts on discrepancy reports, CAPA records, controlled documents, and other Quality topics; represent Quality on multi-disciplinary teams.
  • Perform data verification to ensure accuracy of information presented in Quality Events.
  • Gather supporting documentation for the investigation of Quality Events.
  • Monitor CAPAs to maintain adherence to due dates.
  • Perform Effectiveness Checks for existing CAPAs.
  • Monitor Continuous Improvement pending items and workflows to ensure closure.
  • Update trackers and pull information from Veeva QMS as necessary to ensure Quality Systems team is meeting necessary targets.
  • Collaborate with Lead Specialist and Management to establish and meet targets and timelines.
  • Ability to manage competing priorities with guidance from leadership
  • Follow company policies and procedures.

Minimum Qualifications:
  • Bachelor's degree (preferably in Life Sciences field) or equivalent industry experience
  • 2-4 years of experience in Quality Assurance is required
  • Knowledge of cGMPs or equivalent regulations.
  • Ability to interpret Quality standards for implementation.
  • Skills to independently evaluate situations and propose potential solutions.

Preferred Qualifications:
  • Leverage critical thinking and strong attention to detail
  • Experience in technical writing and editing skills
  • 2+ years of experience in the biopharmaceutical industry (preferably with biologics).
  • Experience in deviation records or CAPA management
  • Ability to work independently
  • Experience in use of quality systems software (quality management systems and/or electronic document management systems).

Position Type/Expected Hours of Work:
This role is a full-time onsite position. Days and hours of work are Monday through Friday 8:00 a.m. to 5:00 p.m. unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $31.63 - $42.16 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

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