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Stability Chemist Jobs (NOW HIRING)

Actalent

Chemist

Omaha, NE

Chemist The Chemist plays a key role in supporting pharmaceutical manufacturing by performing ... Perform stability testing, manage stability samples, and compile clear and comprehensive stability ...

Actalent

Chemist

Omaha, NE

Chemist The Chemist plays a key role in supporting pharmaceutical manufacturing by performing ... Perform stability testing, manage stability samples, and compile clear and comprehensive stability ...

CEDENT

Chemist

Ferndale, MI

Assists QC staff in determining whether or not client products meet release and stability ... Trains chemistry staff as needed. * Writes and revises SOPs as requested by management. * Performs ...

Onsite Personnel LLC

Chemist

Philadelphia, PA

This position's purpose is to support the Quality Control lab for analysis of purified water, raw materials, finished and stability samples. Essential Duties and Responsibilities: QC Chemist * Sample ...

BioPhase Solutions

Chemist III/Sr. Chemist

Anaheim, CA

$40 - $50/hr

Independently execute QC chemistry testing to support routine manufacturing activities, new product method development and stability testing. * Review analytical raw data * Participate in protocol ...

Stark Pharma Solutions Inc

Chemist III

Lakewood, IL · On-site

I am working on Chemist III position right now. Please send me your updated resume if you have ... This role will be responsible for coordinating stability studies, managing reference standard ...

Piney Technical Services

Chemist

Kansas City, MO

Maintains organization's stability and reputation by complying with government regulations, cGMP ... Lab Environment, Microbiology, Biology, Chemistry, Chemistry Techniques, Reporting Results, Safety ...

AllSTEM Connections

Chemist

Darien, CT · On-site

$62K/yr

The contractor will be responsible for requesting standard tests and reviews (stability, salon, PET ... Chemist or Manager. • Document within laboratory notebook and formulation software every batch ...

Talnt

Wet Chemist

Akron, OH

$70K - $95K/hr

Monitor environmental stability chambers and coordinate routine sample collection for internal, microbiological, and third-party laboratory testing. * Maintain accurate formulation records ...

Cedent

Chemist (Ferndale, MI)

Ferndale, MI · On-site

Assists QC staff in determining whether or not client products meet release and stability ... Trains chemistry staff as needed. * Writes and revises SOPs as requested by management. * Performs ...

CEDENT

Chemist (Ferndale, MI)

Ferndale, MI · On-site

Assists QC staff in determining whether or not client products meet release and stability ... Trains chemistry staff as needed. Writes and revises SOPs as requested by management. Performs ...

Lannett Company Inc

Product Chemist I

Seymour, IN · On-site

Perform accurate and timely analysis of in-process, release, and stability samples for drug ... HPLC, GC, dissolution, wet chemistry) Excellent oral and written communication skills Strong ...

Custom Analytics

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Analytical Chemist

Dalzell, SC · On-site

$50K - $75K/yr

We also house a large number of stability chambers for our clients.

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How much do stability chemist jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for stability chemist in the United States is $30.99, according to ZipRecruiter salary data. Most workers in this role earn between $24.04 and $35.58 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a stability chemist?

As a Stability Chemist, your daily responsibilities usually involve preparing and testing pharmaceutical or chemical samples to assess their stability under various environmental conditions, following established protocols and regulatory guidelines. You will analyze results using analytical instruments such as HPLC or GC, document findings in lab notebooks or electronic systems, and report any anomalies to senior scientists or quality teams. The role often requires close collaboration with quality assurance, research and development, and manufacturing colleagues to ensure product integrity and regulatory compliance. Additionally, you may participate in laboratory investigations and support continuous improvement initiatives.

What is a stability chemist?

A Stability Chemist is responsible for testing and analyzing the stability of pharmaceutical products and raw materials over time. They design and conduct stability studies under various environmental conditions to ensure product efficacy, safety, and shelf life. Their work involves following regulatory guidelines, documenting results, and supporting formulation, manufacturing, and quality assurance teams.

What are the key skills and qualifications needed to thrive as a stability chemist?

To thrive as a Stability Chemist, you need a strong background in analytical chemistry, meticulous attention to detail, and at least a bachelor’s degree in chemistry or a related scientific field. Familiarity with laboratory information management systems (LIMS), analytical instrumentation like HPLC and GC, and regulatory guidelines such as ICH, FDA, or GMP is crucial. Strong documentation skills, problem-solving abilities, and effective communication are key soft skills that help you excel. These skills ensure accurate stability testing, regulatory compliance, and successful collaboration across research and quality teams.

Is chemistry a stable job?

A stability chemist typically works in the chemical or pharmaceutical industries, where demand for research, quality control, and product development remains steady. The job often offers regular hours and requires specialized skills, such as laboratory techniques and safety protocols, contributing to its stability. However, job stability can vary based on industry trends and economic factors.
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Stability Chemist jobs near you
Infographic showing various Stability Chemist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, and 5% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $64,466 per year, or $31 per hour.

Supervisor, Chemistry and Stability

Freseniusglobal

Wilson, NC

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 days ago

Job description

Job SummaryThe Chemistry and Stability Supervisor will be responsible for the supervision of daily activities in the Chemistry and Stability Departments. The Chemistry and Stability Supervisor will assure that activities associated with the testing, release, and results reporting of materials, products and components meet established and expected quality, regulatory and customer requirements. This position is also responsible for overseeing the activities of Stability Coordination staff. The position directly interfaces with other QC Laboratory Supervisors responsible for generating data to be reported for stability studies. Additionally, the position is an interdepartmental liaison which supports virtually all aspects of the business, as it relates to the compliance of the stability program, the furnishing of stability information, providing consultation on product behavior, and managing special projects to achieve company initiatives. The Chemistry and Stability Supervisor will regularly interact with departments on site and at a corporate level such as Operations, Packaging, Quality Assurance, Stability, Validation and Regulatory Affairs.
Salary Range: $73,614 - $103,528
Position is eligible to participate in a bonus plan with a target of 6% of the base salary.
Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.Responsibilities
  • Coordinate the training and development of department personnel.
  • Aid in the assignment of personnel Goals & Objectives. Perform personnel reviews and administer disciplinary actions as required.
  • Promote a positive work environment for personnel morale and achievement of goals & objectives. Address personnel issues with assistance from department Management and Human Resources.
  • Prioritize and track progress of daily activities in functional area for timely release of materials, products, components and/or information.
  • Assure that the integrity of materials, products, components and data is maintained.
  • Assure staff conformance with cGMP and FK USA procedures and policies.
  • Facilitate department investigations for non-conforming materials, products and/or components.
  • Support investigations and corrective/preventative actions for the Company.
  • Provide technical guidance on existing and improvements to processes, products, procedures and methods
  • Assist with development and maintenance of department budget.
  • Compile information required for Management Reviews and Audit Responses.
  • Represent department at meetings.
  • Reviews Stability Testing Protocols for accuracy and compliance.
  • Reviews Stability sections of regulatory submissions prior to filing with the agency.
  • Assesses impact of Material Change Requests (MCR) to current stability commitments.
  • Consults with Regulatory Affairs on interpretation and execution of stability commitments.
  • Tracks acquisition of lots into stability program to ensure all required batches are requested and acquired for regulatory requirements.
  • Reviews stability protocols for accuracy.
  • Manages approving, expiry calculation, stability summary, and archiving processes.
  • Reports department metrics for Quality Management purposes as required
  • Assumes area ownership of stability chambers and is responsible for investigating excursions, initiating critical work to be performed, and assessing impact to product stored within.
  • Review and manage the regulatory annual reports
  • Provides laboratory supervision support to assign testing, review documentation, and track completion of assignments.
  • Develops staff to achieve both departmental and personnel goals.
  • Identifies and solves personnel issues.
  • Support investigations (OOS, OOT, Deviations, Complaints, etc.) as required.
  • All employees are responsible for ensuring the compliance to company documents, programs and activities related to the Health, Safety, Environment, Energy, and Quality Management Systems, as per your roles and responsibilities

REQUIREMENTS

  • B.S. in Chemistry or related Science
  • Five - Ten years of progressive pharmaceutical lab experience
  • Equivalent combined of education and experience in pharmaceutical manufac
  • turing, related industrial or clinical experience accepted.
  • Excellent verbal and written communication skills are essential.
  • Knowledge of department processes and procedures, and a clear understanding of regulatory requirements.
  • Demonstrated knowledge of Statistical analysis as it pertains to product stability and determination of shelf-life is plus.
  • A demonstrated ability to lead in a team and effect solutions to accommodate competing goals.
  • Flexibility, adaptability, and strong desire to work in a dynamic environment.
  • Must possess skills to analyze analytical results and solve problems as a backup to Stability Manager
Additional Information

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability,401K with company contribution, andwellness program.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.

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