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Pharmaceutical Stability Jobs (NOW HIRING)

Genezen

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 Specialist III-Stability

Portsmouth, NH · On-site

Minimum of 4 years of hands-on experience managing or supporting GMP stability programs within a pharmaceutical, biotechnology, or other regulated laboratory environment, including the coordination ...

Lonza

QC Specialist II-Stability

Portsmouth, NH

Minimum of 3 years of hands-on experience managing or supporting GMP stability programs within a pharmaceutical, biotechnology, or other regulated laboratory environment, including the coordination ...

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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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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.
Stability Manager, Quality Control

Stability Manager, Quality Control

Genezen

Lexington, MA • On-site

$130K - $150K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago

Job description

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our clients. We provide process development, produce GMP viral vectors, and provide cell transduction for gene and cell therapy clinical trials and are proud to be a part of the process that leads to new cures.
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
The Quality Control Technical Services (QCTS) team manages the lifecycle of analytical methods, including method transfer and validation, stability programs, reference standards, critical reagents, product specifications, and computer systems validation. The Manager, QC Stability provides leadership and strategic oversight of the stability programs from early phase through commercialized programs. This role ensures regulatory compliance, analytical excellence, and effective cross-functional collaboration to maintain product quality throughout the product lifecycle
ESSENTIAL JOB FUNCTIONS
  • Govern the Stability Program on behalf of clients across all early phase, and commercial programs for DS, DP, and diluents
  • Ensure compliance with Quality Agreements and global regulatory expectations
  • Maintain and oversee the Stability Master Planner
  • Monitor and publish stability KPIs
  • Supervise, mentor, and develop team members.
  • Own quality documentation including deviations, CAPAs, and change controls related to stability
  • Manage the revision and approval SOPs, protocols, and reports
  • Conduct audits of stability studies and processes
  • Verify data for accuracy and compliance
  • Summarize and interpret stability data and generate stability trend analysis reports
  • Partner with cross-functional teams for execution of stability studies
  • Identify and implement operational improvements

SPECIAL JOB REQUIREMENTS
  • Proven leadership and cross-functional collaboration skills
  • Ability to manage competing priorities under pressure
  • Highly organized with strong problem-solving skills
  • Clear professional communication and presentation skills
  • Commitment to quality, integrity, and continuous improvement
  • Prior CDMO experience a plus
  • Adaptability required as work schedule may change based on business needs
  • Criminal background check required
  • Other duties as assigned

EDUCATION
  • Education Level: Master's Degree in science-related field

ON-THE-JOB EXPERIENCE
  • 8+ years of industry experience in CDMO
  • Experience managing stability programs for cell/gene therapy products
  • Strong understanding of cGMPs and global regulations
  • Experience managing deviations, CAPAs, and change controls
  • Experience with analytical methods such as potency assays, ELISA, ddPCR, qPCR, SEC-HPLC, and CE-SDS

SKILLS/ABILITIES
  • Prior experience working in a CDMO environment
  • 8+ years working in a Good Manufacturing Practices (GMP) environment
  • Subject matter expert in Good Documentation Practices (GDP)
  • Excellent computer literacy (MS Word, Excel, SmartSheets)
  • Excellent project management tools (MS project, SmartSheets)
  • Excellent executive communication skills, both written and oral

PAY RANGE:The annual salary range for this position is $130,000-$150,000.
PHYSICAL DEMANDS
While performing the duties of this job, the employee is required to meet the following physical demands:
Work Environment
  • Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning
  • Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities
  • Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock
  • Occasionally exposed to extremely loud noise levels
  • Regularly sit for long periods of time

Movement
  • Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms
  • Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl

Lifting
  • Frequently lift and/or move up to 25 pounds
  • Occasionally lift and/or move up to 50 pounds

Vision
  • Frequently utilize close vision and the ability to adjust focus
    Communication
  • Frequently required to communicate by talking, hearing, using telephone and e-mail

GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science
We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients
We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience & Grit in operations
We are committed to overcoming challenges, learning from failures, and persistently striving for success.
Execute with Excellence & Integrity
We are dedicated to delivering quality results and upholding ethical principals.
Solutions driven for our partners
We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
  • Paid vacation days, amount based on tenure
  • Paid sick time
  • 10 observed holidays + 2 floating holiday + 1 volunteer day
  • 401(k) plan with company match up to 6% of salary, vested immediately
  • Share Appreciation Rights
  • Choice of several healthcare plans
  • FSA and HSA programs
  • Dental & vision care
  • Employer-paid basic term life/personal accident insurance
  • Voluntary disability, universal life/personal accident insurance
  • Accidental Death & Dismemberment (AD&D) Insurance

ADDITIONAL DETAILS
  • Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.
  • This position requires a criminal background check.
  • Genezen is an Equal Opportunity Employer.
  • Genezen participates in EVerify.
  • Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.

Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.

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