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Stability Manager, Quality Control

Lexington, MA · On-site

$130K - $150K/yr

The Manager, QC Stability provides leadership and strategic oversight of the stability programs ... Regularly required to work around large machinery and typical utilities seen in pharmaceutical ...

Lonza

QC Stability Coordinator

Tampa, FL

$18.75 - $25.75/hr

Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings. * Knowledge of GMP and stability program requirements, including regulatory guidelines. * Strong ...

Abzena Inc.

QC Stability Manager

San Diego, CA · On-site

Minimum 10 years of experience in QC GMP pharmaceutical or biotechnology laboratories within a cGMP ... and stability studies. Core Competencies: * Excellent written, verbal, and interpersonal ...

Lonza

QC Stability Coordinator

Tampa, FL · On-site

$18.75 - $25.75/hr

Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings. * Knowledge of GMP and stability program requirements, including regulatory guidelines. * Strong ...

Moderna, Inc.

Sr. Manager, CMC Stability

Norwood, MA · On-site

As a stability leader, you will execute phase-appropriate stability strategies across a diverse ... Degree in Life Sciences, Chemistry, Engineering, Pharmaceutical Sciences, or related technical ...

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Pharmaceutical Stability information

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How much do pharmaceutical stability jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for pharmaceutical stability in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What is a Pharmaceutical Stability job?

A Pharmaceutical Stability job involves evaluating the shelf-life and storage conditions of drug products to ensure their potency, safety, and efficacy over time. Professionals in this role conduct stability studies, analyze degradation patterns, and follow regulatory guidelines set by agencies like the FDA and ICH. They work closely with quality control, regulatory, and formulation teams to support product development and approval.

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

To thrive in Pharmaceutical Stability, you need a solid background in pharmaceutical sciences or chemistry, strong analytical abilities, and attention to detail, often underpinned by a bachelor’s or master’s degree in a relevant field. Familiarity with laboratory instrumentation (such as HPLC, GC, and dissolution testers), GMP regulations, and data management systems is essential. Strong organization, problem-solving skills, and effective teamwork and communication abilities set outstanding professionals apart. These skills ensure accurate stability testing, regulatory compliance, and successful collaboration within cross-functional teams in pharmaceutical development.

What are the typical daily responsibilities of someone working in Pharmaceutical Stability?

Professionals in Pharmaceutical Stability are primarily responsible for designing, executing, and documenting stability studies to ensure the quality and shelf-life of pharmaceutical products. Their daily tasks often involve preparing samples, conducting analytical tests using specialized lab equipment, recording data, and interpreting results in accordance with regulatory guidelines. They also collaborate regularly with formulation scientists, quality assurance teams, and regulatory affairs to support product development and submission activities. Attention to detail, adherence to standard operating procedures, and clear communication are essential parts of the job.

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What cities are hiring for Pharmaceutical Stability jobs? Cities with the most Pharmaceutical Stability job openings:
What are the most commonly searched types of Pharmaceutical Stability jobs? The most popular types of Pharmaceutical Stability jobs are:
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Pharmaceutical Stability jobs near you
Infographic showing various Pharmaceutical Stability job openings in the United States as of June 2026, with employment types broken down into 3% As Needed, 50% Full Time, 29% Part Time, and 18% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Supervisor, Chemistry and Stability

Freseniusglobal

Wilson, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 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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