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Quality Control Stability Jobs (NOW HIRING)

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 ...

OOS/OOT trends, stability data, CoAs/QC release testing). * Ensure robust processes for CoA generation, review, and approval processes for clinical and commercial materials ensuring analytical data ...

QC Chemist

Pearl River, NY · On-site

$55K - $95K/yr

Monitors Stability chambers, Photostability chamber, freezers, refrigerators etc. * Performs ... Train other QC chemists in a timely manner on all the general Laboratory SOPs and test methods.

Supervise the testing of bulk release, finished product and stability testing * Manage and supervise QC laboratory personnel with varying levels of experience, assigning the work schedule and ensure ...

The Quality Control (QC) Manager is responsible for leading and managing Quality Control laboratory ... Supervise and participate in stability programs, method transfers, and analytical method ...

Oversee all analytical testing for manufacturing, release, and stability. * Review and interpret ... Develop and mentor QC staff through training and performance development. * Support continuous ...

Oversee all analytical testing for manufacturing, release, and stability. * Review and interpret ... Develop and mentor QC staff through training and performance development. * Support continuous ...

Be Seen First

This position will support El Paso's Quality Control Laboratory by performing microbiological testing on raw materials, in-process product, finished products, and stability samples to achieve QC ...

New

The Quality Control (QC) Manager is responsible for leading and managing Quality Control laboratory ... Supervise and participate in stability programs, method transfers, and analytical method ...

Experience working in a QC or analytical laboratory supporting release and stability testing ... Familiarity with high-throughput assays such as endo- and exonuclease testing and genomic DNA ...

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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 31, 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 Planner

$19.50 - $27/hr

Full-time

Posted 11 days ago


Job description

Purpose and Scope:

The QC Planner is responsible for the management, planning and coordination of samples in the QC laboratory. This position will coordinate and communicate across QC and other departments to organize and maintain tracking of testing stages to ensure accurate and timely reporting.

Essential Duties & Responsibilities:

  • Perform scheduling of all workstreams to ensure optimum flexibility and utilization of all employees to meet the demands of the business.
  • Ensure all testing is scheduled to meet timelines for stability commitments, production and ship dates.
  • Facilitate cross-training to prevent potential bottlenecks in testing efficiencies.
  • Maintain a customer-focused sample management and planning system in the QC laboratory with the assistance of the QC Management team.
  • Collaborate with external departments to ensure swift communication of delays and impact to production or shipment schedules.
  • Communicate with management and manufacturing to assist in timely release of critical samples, coordinate results reporting activities with QC customers and follow up with Stability area for timely delivery of samples for stability testing.
  • Review samples and accompanying documentation submitted to the QC laboratory to ensure accuracy.
  • Provide support to the QC department for the evaluation and implementation of new technological innovations in laboratory automation systems, documentation systems and other technologies.
  • Ensure the stability pulls schedule are mitigated and designed with the most efficient test batching potential to support adherence to testing timelines prior to stability samples being pulled and submitted to the laboratory.
  • Support revisions of Binocs scheduling software including revising test times, scheduling rules, and templating new materials in the system.
  • Provide critical information on workload assignments, and manage test scheduling conflicts and gaps.
  • Establish and track key performance indicators for laboratory activities and introduce operational efficiency efforts in test management.
  • Support QC management by tracking relevant data and assisting with ongoing capacity analysis activities.
  • Contribute to a highly productive environment by avoiding distractions.
  • Maintain a positive atmosphere of teamwork, camaraderie and respect towards co-workers.
  • Ensure that company compliance and regulatory data integrity guidelines are consistently followed.
  • Assist co-workers with the completion of tasks; learn to identify areas of contention on a team and work with management to correct.
  • Interact respectfully with all other employees both inside and outside of the department and members of management, and show interest in others' input and reasoning. Appropriately resolve differences of opinion.
  • Upon delegation, may be responsible for representing the QC laboratory when communicating with outside departments and vendors.
  • Identify issues and possible solutions and escalate those issues and solutions to the department senior leadership or management as appropriate. Follow up as needed to ensure complete resolution.
  • Participate in required annual department related trainings and activities.
  • Perform various other duties as assigned.

Knowledge, Skills & Abilities

  • Demonstrated knowledge of scheduling multiple work streams pertaining to specific products and assays conducted in a high throughput QC laboratory.
  • Strong sense of purpose and drive to meet deadlines without sacrificing quality.
  • Ability to schedule work for multiple workstreams utilizing trained team members as efficiently as possible to reduce cycle time of submitted samples.
  • Ability to perform designated duties under minimal supervision and support departmental management in all aspects of organizational functions.
  • High level of proficiency in Quality Control laboratory procedures and testing techniques.
  • Excellent verbal and written communication skills demonstrated through interactions internally and externally.
  • Ability to manage multiple projects concurrently and under tight time constraints.
  • Ability to grasp and use multiple complex software systems in order to generate and revise a weekly schedule.
  • Understanding of cGMP regulations as it pertains to stability programs.
  • Knowledge of different laboratory instruments as it pertains to scheduling and batching rules.
  • Knowledge of computer applications, including Microsoft Office.
  • Adaptable to shift priorities and to operate with a sense of urgency while maintaining high quality in order to meet important timelines in a high throughput lab.

Core Values

The QC Planner is expected to operate within the framework of Tolmar’s Core Values:

  • Center on People: We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together.
  • Are Proactive & Agile: We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.
  • Act Ethically: We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace.
  • Constantly Improve: We are committed to a collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality.
  • Are Accountable: We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.

Education & Experience

  • Bachelor’s degree in Science, Engineering, Business or related discipline preferred; or equivalent combination of education and experience.
  • Two or more years of experience in an analytical laboratory position.
  • Project management experience and/or certification preferred.

Working Conditions

  • Business demands may present a need to work extended hours.
  • This position will be on-site, with a possibility of a hybrid work arrangement.

Compensation and Benefits

  • Pay: $39.00 - $40.50 per hour
  • Benefits summary: https://www.tolmar.com/careers/employee-benefits

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.


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About Tolmar

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Fort Collins, CO, US

Year founded

2006