ZipRecruiter

Log In

1

Hourly Qc Stability Jobs (NOW HIRING)

TekWissen LLC

QC Analyst I

Vacaville, CA · On-site

$20 - $25/hr

Onsite Summary The QC Stability Study Coordinator I is responsible for overseeing stability program management in compliance with cGMP regulations, with limited supervision. This role includes ...

Biogen

NC · On-site

$178K - $245K/yr

As the Director of Global QC Systems and Stability, you will be at the helm of a global quality control department that plays a critical role in supporting both manufacturing operations and release ...

Vaxcyte

Stability Manager

San Carlos, CA

$147K - $171K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

Thorne

Quality Control Inspector

Summerville, SC · On-site

$19 - $21.25/hr

Our hourly quality control inspector roles offer hands-on experience in a clean, safe, and innovative manufacturing environment with opportunities for growth and development. Whether examining ...

Moderna Therapeutics

... lead QC testing activities across drug substance and drug product, spanning chemistry, microbiology, and bioassay disciplines. You will oversee stability programs and sample management, ensuring ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$134K - $162K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

Novartis

Senior Expert Stability

East Hanover, NJ

$118K/yr

Data management to support the Stability Programs including the administration and distribution of Quality Control (QC) stability samples, associated document coordination, and collection and ...

next page

Showing results 1-20

All JobsHourly Qc Stability Jobs

Hourly Qc Stability information

See salary details

$11

$21

$33

How much do hourly qc stability jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for hourly qc stability in the United States is $21.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What is the difference between Hourly Qc Stability vs Hourly Qc Analyst?

AspectHourly Qc StabilityHourly Qc Analyst
CredentialsTypically requires a high school diploma or equivalent, with on-the-job trainingRequires a degree in science or related field, often with certifications in quality control
Work EnvironmentLaboratory or manufacturing settings, repetitive tasksLaboratory or production environments, analytical work
Industry UsageCommon in manufacturing, pharmaceuticals, food productionUsed in similar industries, often with more analytical responsibilities

Hourly Qc Stability focuses on maintaining product stability over time, often with less formal education. Hourly Qc Analyst involves more analytical testing and requires relevant scientific credentials. Both roles are vital in quality control but differ in complexity and qualifications.

More about Hourly Qc Stability jobs
What cities are hiring for Hourly Qc Stability jobs? Cities with the most Hourly Qc Stability job openings:
What are the most commonly searched types of Qc Stability jobs? The most popular types of Qc Stability jobs are:
What job categories do people searching Hourly Qc Stability jobs look for? The top searched job categories for Hourly Qc Stability jobs are:
Hourly Qc Stability jobs near you
Infographic showing various Hourly Qc Stability job openings in the United States as of May 2026, with employment types broken down into 50% Full Time, 42% Part Time, and 8% Temporary. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $44,668 per year, or $21.5 per hour.
Stability Coordinator/Associate QC Chemist

Stability Coordinator/Associate QC Chemist

Eagle Labs, Inc

Seminole, FL • On-site

$45K - $65K/yr

Full-time

Posted 18 days ago

Job description

Overview:

The Stability Coordinator/Associate Chemist is responsible for the administration of the stability program which includes, scheduling of the stability sample pull points, pulling samples, scheduling and sending out samples for testing, monitoring environmental stability storage chambers and setting the samples down on stability according to the relevant procedures, supporting the site's Stability Program coordinating sample management activities, and ensuring compliance with cGMP, SOPs, and ICH guidelines.

Additional responsibilities are to perform testing, review, approve data, ensure cGMP/GLP practices are following regulatory requirements, equipment management/maintenance, lead investigations, deviations, out-of-specifications (OOS). Collaborate with Quality control manager, director and other departments.

Requirements:

  • The successful candidate must be able to work independently on multiple projects and meet established timelines
  • Applicant must have a bachelor's degree with at least 3-5 years of experience
  • Stability program experience required
  • Relevant Quality experience, preferably in the bio/pharmaceutical/supplemental and/or nutraceutical industry
  • Knowledge of stability and cGMPs
  • An understanding of stability testing, FDA, ICH, and applicable stability regulations is required
  • Knowledge in statistical concepts for appropriate interpretation of stability data (e.g. trending analysis)
  • Strong technical writing skills
  • Proficiency with computer systems (Microsoft Office applications)
  • Experience with document management systems
  • Strong interpersonal and communication (written and oral) skills and the ability to work well in a team environment are essential)
  • Normal lifting, sitting, standing and walking requirements to facilitate support of staff in the office

Responsibilities:

  • In this role, you will play a crucial role in our quality control process, providing support for stability studies and ensuring compliance with regulatory guidelines
  • Conducting and overseeing stability studies to ensure product quality and compliance with regulatory guidelines
  • Providing support for product testing and analysis, including sample preparation, data analysis, and report writing
  • Maintaining and updating quality control documentation and record
  • Identifying and resolving quality control issues and deviations in a timely manner
  • Collaborating with cross-functional teams to ensure timely completion of projects and adherence to quality standards
  • Communicating with external vendors and suppliers to ensure timely delivery and quality of materials and with outside contract laboratories on testing.
  • Schedule testing and sending out samples to contract laboratories and maintaining communication and follow ups on status and results
  • Participating in internal and external audits and inspections
  • Staying up to date with industry regulations and guidelines related to quality control
  • Participating in continuous improvement initiatives to enhance quality control processes and procedures
  • Prioritizing and managing multiple tasks and projects to meet deadlines
  • Ensuring compliance with company policies and procedures
  • Enter studies into the computerized stability management system in accordance with SOPs.
  • Compile, interpret, and evaluate data and identify impacts related to deviations, OOS/OOT results, or excursions.
  • Maintain inventory, coordinate final sample destruction, and reconcile stability materials.
  • Prepare samples for shipment, complete related documentation, and perform peer reviews.
  • Ensure compliance with cGMP, quality policies, and guidelines.
  • Review internally and externally produced laboratory data for finished products and raw materials.
  • All other duties as assigned.

Education:

  • Bachelor’s degree in related scientific discipline and 4-5 years of experience with documentation systems and cGMP-compliant environments required.
  • Experience with sample tracking is preferred.
  • Strong organizational, technical writing, and communication skills.
  • Knowledge of stability program expectations, sample handling, data integrity, and QMS principles.
  • Proficiency with Microsoft Outlook, Excel, and Word.

Apply