ZipRecruiter

Log In

1

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 ...

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 ...

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

$134.60K - $162.40K/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 · On-site

$118.40K/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 ...

Moderna Therapeutics

$25.50 - $34.50/hr

This role sits at the intersection of Quality Control Chemistry and global stability programs, driving the analytical backbone that ensures product quality and compliance. It combines hands-on ...

Tolmar

Quality Control Planner

Fort Collins, CO

$19.25 - $26.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC ... Ensure the stability pulls schedule are mitigated and designed with the most efficient test ...

Tolmar

Quality Control Planner

Windsor, CO · On-site

$39 - $40.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC ... Ensure the stability pulls schedule are mitigated and designed with the most efficient test ...

Tolmar

Quality Control Planner

Windsor, CO

$19.50 - $27/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC ... Ensure the stability pulls schedule are mitigated and designed with the most efficient test ...

Tolmar Inc.

Quality Control Planner

Fort Collins, CO · On-site

$19.25 - $26.50/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC ... Ensure the stability pulls schedule are mitigated and designed with the most efficient test ...

Tolmar Inc.

Quality Control Planner

Windsor, CO · On-site

$19.50 - $27/hr

The QC Planner is responsible for the management, planning and coordination of samples in the QC ... Ensure the stability pulls schedule are mitigated and designed with the most efficient test ...

next page

Showing results 1-20

People also search for

All JobsQc Stability Jobs

Qc Stability information

See salary details

$30.5K

$81.3K

$129.5K

How much do qc stability jobs pay per year?

As of Jun 3, 2026, the average yearly pay for qc stability in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What is a QC Stability job?

A QC Stability job focuses on monitoring and evaluating the stability of pharmaceutical products over time to ensure they maintain their quality, safety, and efficacy. Responsibilities typically include designing stability studies, analyzing samples at different time points, and documenting results in compliance with regulatory guidelines (e.g., ICH, FDA). QC Stability professionals work closely with quality control and regulatory teams to ensure data integrity and provide critical information for product shelf-life determination.

What are the key skills and qualifications needed to thrive in the Qc Stability position, and why are they important?

To thrive as a QC Stability professional, you need a solid background in chemistry, analytical testing, and good documentation practices, typically supported by a degree in life sciences or related field. Familiarity with laboratory information management systems (LIMS), chromatography software (such as HPLC or GC), and regulatory guidelines like GMP and ICH is essential. Strong attention to detail, problem-solving abilities, and effective communication skills are key soft skills in this role. These competencies ensure accurate data analysis, regulatory compliance, and efficient teamwork in maintaining product quality over time.

What are the typical day-to-day responsibilities of a QC Stability professional?

A QC Stability professional is responsible for managing stability studies on pharmaceutical products, which includes preparing stability samples, testing products at specified intervals, analyzing and documenting results, and ensuring data integrity. This role often involves working closely with cross-functional teams such as quality assurance, production, and research and development to address any findings or deviations. You can expect to spend time in the laboratory conducting tests, as well as at your desk compiling reports and supporting regulatory submissions. The position requires meticulous organization and the ability to handle multiple studies simultaneously, making time management a valuable asset.
More about Qc Stability jobs
What cities are hiring for Qc Stability jobs? Cities with the most 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 states have the most Qc Stability jobs? States with the most job openings for Qc Stability jobs include:
What job categories do people searching Qc Stability jobs look for? The top searched job categories for Qc Stability jobs are:
Qc Stability jobs near you
Infographic showing various Qc Stability job openings in the United States as of May 2026, with employment types broken down into 7% As Needed, 86% Full Time, and 7% Part Time. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $81,324 per year, or $39.1 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 12 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