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Quality Control Stability Jobs (NOW HIRING)

$25.50 - $34.50/hr

As a QC Analyst, you will also support global GMP stability programs through a variety of operational and technical activities, including sample set downs, pulls, shipments, data trending and ...

QC Specialist III-Stability Location: This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 7:00 AM-4:00 PM EST. What you will get: Below you will ...

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 ...

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 ...

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 ...

... 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 ...

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

$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 ...

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 ...

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 ...

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 ...

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 ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and Manufacturing to meet production timelines Requirements * 6-8+ years of pharmaceutical QC experience (cGMP ...

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Quality Control Stability information

See salary details

$30.5K

$81.3K

$129.5K

How much do quality control stability jobs pay per year?

As of May 30, 2026, the average yearly pay for quality control 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 are the key skills and qualifications needed to thrive as a Quality Control Stability specialist, and why are they important?

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

What are some common challenges faced in a Quality Control Stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

What is a Quality Control Stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.

What is the difference between Quality Control Stability vs Quality Control Inspector?

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

More about Quality Control Stability jobs
What cities are hiring for Quality Control Stability jobs? Cities with the most Quality Control Stability job openings:
What are the most commonly searched types of Quality Control Stability jobs? The most popular types of Quality Control Stability jobs are:
What states have the most Quality Control Stability jobs? States with the most job openings for Quality Control Stability jobs include:
Quality Control Technician

Quality Control Technician

PHARMALOGIC HOLDINGS

Idaho Falls, ID • On-site

$30 - $34/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago


Job description

Job Title: Quality Control Technician

FLSA Status: Non-Exempt

Position Type: Full Time

Pay Type: Salary - Hourly


PharmaLogic is the fastest-growing SPECT & PET radiopharmaceutical solutions provider and contract development and manufacturing organization (CDMO) with radiopharmacies across North America. We are passionate about expanding the power of radiopharmaceutical technology to provide transformative diagnostic and therapeutic agents to patients from bench to bedside.

Role Summary:

As a QC Technician, you will play an essential role in the development, implementation, and validation for new radiopharmaceuticals, radiochemical and isotope production. The position will have hands-on experience with radiochemistry synthesis, purification, and formulation for imaging and biodistribution studies; executing studies in parallel; and working alongside other laboratory scientists.

Job Responsibilities and Duties:

  • Responsible for production of radiotracers:
  • Synthesis of generic and novel radiopharmaceuticals.
  • Purification of small and large molecules.
  • Maintain involvement with training and transfer of methods to and from QC and contract manufacturers as assigned.
  • Adapt, operate and maintain analytical instrumentation to produce accurate results.
  • Operate and maintain automated radiochemistry synthesis units.
  • Maintain experience with broad range isotopes and labeling methods and increase personal scientific, regulatory and compendial expertise.
  • Work with appropriate personnel to support, install, and qualify equipment on-site.
  • Assist with continuous improvement of current cGMP and non-GMP processes.
  • Follow all SOP guidelines for QC release testing of radiopharmaceutical products, raw material, finished and semi-finished products, environment, and facilities.
  • Modify and validate analytical procedures to meet QC needs.
  • Prepare chemical reagents for manufacturing and QC needs.
  • Maintain clean and safe work environment, performing radiation safety duties in compliance with safety and pharmaceutical regulations. Always demonstrate good safety practices including the appropriate use of protective equipment.
  • Support design and development of experimental protocols and procedures consistent with cGMP and cGLP.
  • Assist in QC stability testing, prepare and maintain stability records and summaries.
  • Perform other job-related duties as assigned.

Job Requirements │ Skills │ Education:

  • Requires a bachelor’s degree in chemistry, Radiology, Nuclear Medicine, Nuclear Physics, Nuclear Engineering or related fields.
  • 3-5 years of working in a GMP manufacturing environment and with FDA cGMP regulations required.
  • Experience with laboratory procedures and radiochemistry techniques (separation techniques – SPE) and analytical method, equipment (ICP-MS, ICP- OES, GC, TLC, and radiometric measures) highly favored.
  • Experience with HPLC, radiochemistry synthesis, US FDA cGMP, Radiation Safety Principles, Isotopes production and analytical equipment troubleshooting and maintenance a plus.
  • Superior teamwork, multi-tasking, and time/project management skills.
  • Excellent communication, analytical, problem solving, presentation and computer/PC skills (including proficiency in Microsoft Suite and related software).
  • Ability to work varying shifts and travel up to 10%.

Physical and Intellectual Requirements:  

Required are a mechanical aptitude; manual dexterity for manipulating small items; ability to lift up to 50 lbs. and to handle frequent crawling, stooping, crouching and kneeling; ability to analyze situations, set priorities and meet deadlines while maintaining attention to detail in a fast-paced and dynamic environment; effective organizational skills; a commitment to continuous learning; an ability to work well both independently and as part of a team.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other protected class.

Benefits Include:

  • 401(k) retirement benefit program

  • Medical

  • Dental care

  • Disability insurance

  • Employee assistance program

  • Extended health care

  • Life insurance

  • On-site parking

  • Paid time off

  • Vision care


8 am to 4 pm or 9 am to 5 pm
40/week