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Stability Program Assistant Coordinator Jobs (NOW HIRING)

Lonza

QC Stability Coordinator

Tampa, FL · On-site

$18.75 - $25.75/hr

QC Stability Coordinator Location: Tampa, FL (on-site) Today, Lonza is a global leader in life ... Compensation programs that recognize high performance. * Medical, dental and vision insurance.

JCCA

Program Assistant

Bronx, NY · On-site

$24.72/hr

Services are team-based and highly coordinated, family-driven and youth-guided, focused on improving stability, functioning, and long-term well-being. Position Summary The Program Assistant is a key ...

Philly Peace In Progress

Program Assistant

Philadelphia, PA · On-site

$37K - $47K/yr

... stability and success. Position Overview We are seeking dedicated individuals who have a passion ... As a Volunteer Program Assistant, you will support the planning, coordination, and delivery of our ...

California State University

$2.7K/mo

College Link Program Assistant Coordinator - Part-Time (ASC II) Apply now Job no: 560526 Work type: Staff Location: East Bay Categories: Unit 7 - CSUEU - Clerical and Administrative Support Services ...

US VETS Inc

Program Assistant

Inglewood, CA · On-site

$21.78 - $25/hr

... path to stability and independence. As a Program Coordinator, you will play a vital role in ... * Assist Case Managers and program staff with file maintenance, audit preparation, and quality ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$147K - $171K/yr

... assist with leading the functionality and maintenance of stability related processes and systems. * Drives continuous improvement activities for the clinical stability programs. * Ensures that the ...

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Stability Program Assistant Coordinator information

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How much do stability program assistant coordinator jobs pay per year?

As of Sep 12, 2026, the average yearly pay for stability program assistant coordinator in the United States is $54,198.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,000.00 and $63,500.00 per year, depending on experience, location, and employer.

What is a stability program assistant coordinator job description?

A stability program assistant coordinator supports the implementation and management of programs aimed at maintaining stability for clients or communities. The role involves coordinating activities, monitoring progress, and collaborating with team members, often requiring organizational skills and familiarity with program management tools. They may also assist with data collection and reporting to ensure program goals are met.

What are popular job titles related to Stability Program Assistant Coordinator jobs?

For Stability Program Assistant Coordinator jobs, the most frequently searched job titles are:

Infographic showing various Stability Program Assistant Coordinator job openings in the United States as of September 2026, with employment types broken down into 73% Full Time, and 27% Part Time. Highlights an 100% In-person job distribution, with an average salary of $54,198 per year, or $26.1 per hour.

QC Stability Coordinator

Tonawanda, NY • On-site

Pine Pharmaceuticals
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Pine Pharmaceuticalsexternal

$26/hr

Full-time

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

Job description

Position Summary:

The Stability Coordinator is responsible for implementing and maintaining Pine Pharmaceuticals' stability study program, including equivalency, initial and recurring annual stability studies, in support of the Quality Control Department. This role owns the full lifecycle of stability testing operations, from sample accessioning and time point allocation through pulling, data delivery, reporting, and trending, ensuring each step is executed on schedule and in accordance with approved protocols, procedures, and applicable ICH guidelines.

The Coordinator generates and maintains stability SOPs, protocols, and summary reports (interim and final), manages stability projects within the ERP system, and maintains sample inventory while coordinating submissions both internally and with external partners. This position also serves as a key point of communication for the stability program, publishing the monthly stability pull dashboard, supporting chamber organization, and reviewing test results to identify and help investigate out-of-trend or out of specification findings.

Success in this role requires close collaboration with QC analysts, QA, and other departments to support investigations, management review, and regulatory audits, while maintaining strict compliance with cGMP and safety requirements. The Stability Coordinator is expected to manage multiple concurrent projects, contribute to continuous quality improvement initiatives, and uphold the data integrity and reliability of the stability program as it relates to product quality and regulatory compliance.


Essential Functions:

  • Generate and support stability SOPs, protocols, and summary reports (interim and final).
  • Ensure timely completion of stability time point pulls as required per applicable protocols and procedures.
  • Manage projects within the ERP system for initial and annual stability studies.
  • Maintain stability sample inventory and coordinate sample submissions, both internally and externally.
  • Support product equivalency studies, including material risk assessments.
  • Publish and disseminate the monthly stability pull dashboard to applicable groups and analysts.
  • Ensure stability chamber organization and maintenance, and support troubleshooting.
  • Support and assist with metrics for stability studies in support of investigations and management review.
  • Review stability test results, identify out-of-trend results; support ongoing investigations.
  • Ensure on-schedule data delivery for study time points per procedure.
  • Support stability data trending in accordance with stability program SOPs and ICH guidelines.
  • Ensure compliance with cGMP and safety requirements.
  • Participate in continuous quality improvements.
  • Support regulatory audits of the Quality Control Department.
  • Perform other duties as determined to support the laboratory.


Education and Experience:

  • Bachelor's degree of science preferred; relevant work experience in pharmaceutical manufacturing.
  • 3-5 years of related work experience preferred in a laboratory environment or pharmaceutical environment.
  • Experience with cGMP 21 CFR 11/210/211/820 Quality Systems.


Knowledge, Skills and Abilities:

  • Excellent organizational, verbal, and written communication skills.
  • Ability to effectively communicate with multiple levels within the organization.
  • Ability to work on multiple projects simultaneously.
  • Knowledge of International Conference on Harmonization (ICH) guidelines and current Good Manufacturing Practice (cGMP).
  • Experience with Microsoft Office and LIMS preferred.

Apply