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Qa Ra Coordinator Jobs (NOW HIRING)

AMRI

Senior Quality Assurance Specialist

Rensselaer, NY · On-site

$103K - $129K/yr

Manage the Internal Audit program including coordination of auditors within the QA department ... Minimum 8 years QA, RA or Compliance experience in pharmaceutical industry (preferred in APIs) at ...

ABO Plasma

Quality Assurance Coordinator

Laredo, TX · On-site

Report monthly to Director of RA/QA * Accept other assignments as delegated by Manager. * Adhere to ... Coordinator). * Successfully complete the required Q.A. training program. * Organizational and ...

ABO Plasma

Quality Assurance Coordinator

Laredo, TX · On-site

Report monthly to Director of RA/QA * Accept other assignments as delegated by Manager. * Adhere to ... Coordinator). * Successfully complete the required Q.A. training program. * Organizational and ...

GardaWorld

Quality Assurance Coordinator

Brentwood, MO · On-site

$60K/yr

Quality Assurance Coordinator Driving Quality Assurance Across Operations & Security! The Quality Assurance Coordinator plays a key role in ensuring operational excellence by supporting quality ...

GardaWorld

Quality Assurance Coordinator

Brentwood, MO · On-site

$60K/yr

Quality Assurance Coordinator | Driving Quality Assurance Across Operations & Security! The Quality Assurance Coordinator plays a key role in ensuring operational excellence by supporting quality ...

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How much do qa ra coordinator jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for qa ra coordinator in the United States is $26.56, according to ZipRecruiter salary data. Most workers in this role earn between $20.91 and $30.53 per hour, depending on experience, location, and employer.

What is a QA RA coordinator?

QA RA Coordinators are professionals who support quality assurance (QA) and regulatory affairs (RA) activities within industries such as pharmaceuticals, medical devices, or biotechnology. They help ensure that products comply with relevant regulations and quality standards, assist in preparing and maintaining necessary documentation, and coordinate audits and inspections. Their work is essential in helping companies meet legal and quality requirements to bring safe and effective products to market.

What are the key skills and qualifications needed to thrive as a QA RA coordinator?

To thrive as a QA/RA Coordinator, you need a solid understanding of quality assurance and regulatory affairs principles, often supported by a degree in life sciences or related fields. Familiarity with quality management systems (such as ISO 13485), regulatory submission processes, and document control software is typically required. Attention to detail, organization, and strong communication skills help ensure compliance and effective coordination across teams. These skills are vital for maintaining regulatory compliance, product quality, and smooth operations within highly regulated industries.

What are some common challenges faced by a QA RA coordinator when managing documentation for regulatory submissions?

QA/RA Coordinators often face challenges in ensuring that all documentation for regulatory submissions is complete, accurate, and formatted according to specific agency requirements. Coordinating input from multiple departments, keeping up with changing regulations, and meeting tight deadlines can be particularly demanding. Successful coordinators use strong organizational skills and clear communication to keep processes streamlined and to avoid delays or compliance issues. Collaboration with cross-functional teams is essential to gather necessary data and resolve discrepancies quickly.

What is the difference between Qa Ra Coordinator vs Qa Analyst?

AspectQa Ra CoordinatorQa Analyst
CertificationsISO, Six Sigma, or industry-specific quality certificationsISO, Six Sigma, or quality assurance certifications
Work EnvironmentManufacturing, healthcare, or software development teamsQuality assurance departments across various industries
Employer UsageUsed by companies managing regulatory compliance and quality processesUsed by organizations analyzing quality data and testing outcomes

The Qa Ra Coordinator primarily manages quality and regulatory documentation, ensuring compliance, while the Qa Analyst focuses on analyzing quality data to identify issues. Both roles require similar certifications and often work in related environments, but their core responsibilities differ: coordination versus analysis.

What cities are hiring for Qa Ra Coordinator jobs?

Cities with the most Qa Ra Coordinator job openings:

What are the most commonly searched types of Qa Ra jobs?

The most popular types of Qa Ra jobs are:

What states have the most Qa Ra Coordinator jobs?

States with the most job openings for Qa Ra Coordinator jobs include:

What are popular job titles related to Qa Ra Coordinator jobs?

For Qa Ra Coordinator jobs, the most frequently searched job titles are:

QA RA Director Consulting Position

Charleston, WV

ProPharma Group
Business Management Consulting • 51 - 200 employees
Learn more about ProPharma Groupexternal

Full-time

Posted 27 days ago

Key responsibilities

  • Assess draft platform roadmaps, identify gaps, and recommend lead platforms to build a phased, gated GMP readiness plan.

  • Guide and help execute design controls, FMEA, and IQ/OQ/PQ strategies for combined instrument, consumable, and software systems, including documentation if needed.

  • Advise on the development and refinement of the 21 CFR Part 11 roadmap, including decision-making on offline versus cloud-based analysis.

Job description

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

Our Biologics client builds instruments, software, hardware consumables, and biological consumables for functional cell-based assays. They have a lean team in need of an experienced strategic advisor to help build out and execute their GMP readiness plan so their first GMP-ready product can reach customers sooner and more efficiently

GMP Platform roadmap

  • Assess our draft 3-platform roadmap, gaps, timelines, and risks
  • Recommend which platform to lead with
  • Build a phased, gated roadmap with a defensible "launch line" for when it can credibly be sold for GMP use
  • Guide (and where needed help execute) design controls, design FMEA, and an IQ/OQ/PQ strategy for a combined instrument, consumable, and software system
  • (Possible) hand-on building of DQ/IQ/OQ/PQ documentation

21 CFR Part 11 roadmap

  • Review & refine our existing Part 11 roadmap
  • Advise as needed on Part 11 execution plans
  • Provide critical input into decision of offline versus cloud-based analysis

QMS Build-out - Instruments, HW Consumables, Biological Consumables, Software

  • Guide a lean QMS spanning all four product elements
  • Address the quality manual, SOPs, document control, supplier qualification, COAs, and how to handle batch-to-batch consumable variability and single-source component risk
  • Choose eQMS (or direct DIY eQMS)
  • (Possible) hands-on implementation of QMS and its elements (e.g. drafting SOPs, etc)

Organizational Quality Strategy

  • Help determine org strategy for scaling Quality & Regulatory function (identify key remaining gaps; map out which hires to make when; internal vs external support)
  • (Possible) Customer-facing Quality & Regulatory leader
  • Lending credibility to Quality & Regulatory strategy for customers considering investing in our platform prior to GMP-readiness
  • Engage with customers to gather critical VoC inputs to GMP-readiness

Requirements:

  • 10+ years in quality, regulatory, or GxP leadership within life sciences
  • GMP (21 CFR 211), 21 CFR 11, ISO 9001,eQMS implementation
  • Has built quality systems from the ground up - ideally for startups
  • Understands how drug manufacturers qualify and adopt supplier technologies for GMP workflows
  • Led QA for GMP drug manufacturer, has qualified vendor analytical assays
  • Vendor-side, taking scientific instruments from R&D into GMP-ready state for pharma/biotech customers.
  • Uses right-sized approach (i.e. lean where appropriate; careful not to overbuild)
  • Experience supporting products that combine instrumentation, software, biological consumables, and hardware consumables.

#LI-JH1#LI-ONSITE

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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