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Qc Stability Manager Jobs (NOW HIRING)

Biogen

NC · On-site

$178K - $245K/yr

Your leadership will guide the department in managing Contract Laboratory Management, Planning and Scheduling, QC Enterprise System Management (LIMS), Specification/Stability programs, and Reference ...

Granules

Quality Control Manager

Chantilly, VA · On-site

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 ...

PL Developments

Quality Control Manager

Miami, FL

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 ...

PL Developments

Quality Control Manager

Miami, FL · On-site

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 ...

Pathway Talent Partners

QC Manager

Norwalk, CT

$100K - $130K/yr

Quality Control Manager - Heavy Civil Construction We are working with a well-established ... PTO + long-term stability with a growing contractor * Opportunity to work on large, high-impact ...

ENFRA LLC

Quality Control Manager

Rayville, LA

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview As a Quality Control Manager, your role encompasses overseeing and ...

ENFRA LLC

Quality Control Manager

West Memphis, AR

At ENFRA, stability, innovation, and growth are more than just values-they are the pillars of our continued success. Overview As a Quality Control Manager, your role encompasses overseeing and ...

Moderna Therapeutics

Reporting to the Associate Director of Quality Control, you will lead QC testing activities across ... Own and manage stability programs, including protocol execution, data trending, and reporting to ...

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Qc Stability Manager information

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How much do qc stability manager jobs pay per year?

As of Jun 8, 2026, the average yearly pay for qc stability manager 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 typical challenges faced by a QC Stability Manager in coordinating stability studies across multiple products?

QC Stability Managers often encounter challenges in managing multiple stability studies simultaneously, particularly when dealing with diverse product portfolios and strict regulatory timelines. Ensuring data integrity, timely sampling, and accurate documentation can be complex, especially when collaborating with cross-functional teams such as manufacturing, regulatory affairs, and quality assurance. Effective organization, proactive communication, and a strong understanding of regulatory requirements are essential for overcoming these challenges and maintaining compliance.

What are QC Stability Managers?

QC Stability Managers are professionals responsible for overseeing the stability testing programs within pharmaceutical, biotechnology, or related industries. Their primary role is to ensure that products maintain their safety, efficacy, and quality throughout their shelf life by managing stability studies, analyzing data, and ensuring compliance with regulatory guidelines. They coordinate cross-functional teams, manage documentation, and ensure that stability protocols meet industry standards. QC Stability Managers also play a crucial role during audits and regulatory submissions by providing necessary data and reports. Their expertise helps companies maintain product quality and meet both internal and external regulatory requirements.

What are the key skills and qualifications needed to thrive as a QC Stability Manager, and why are they important?

To thrive as a QC Stability Manager, you need a robust background in chemistry or pharmaceutical sciences, experience in stability testing, and a relevant degree such as a BS or MS. Familiarity with laboratory information management systems (LIMS), regulatory guidelines (ICH, FDA), and analytical testing equipment like HPLC is essential. Strong organizational, leadership, and communication skills help manage teams, timelines, and cross-functional collaborations. These skills ensure the integrity of stability programs and compliance with regulatory standards, which are critical for product quality and approval.

What is the difference between Qc Stability Manager vs Qc Analyst?

AspectQc Stability ManagerQc Analyst
CertificationsQuality certifications, stability testing trainingQuality certifications, laboratory training
Work EnvironmentLaboratory, quality control departmentsLaboratory, testing facilities
Employer & IndustryPharmaceutical, biotech, or chemical industriesPharmaceutical, biotech, or chemical industries
Primary FocusOverseeing stability programs, ensuring product shelf-lifePerforming stability testing, data analysis

The Qc Stability Manager focuses on managing stability programs and ensuring product shelf-life compliance, while the Qc Analyst conducts stability testing and analyzes data. Both roles require similar certifications and work in laboratory environments within the pharmaceutical or biotech industries, but their responsibilities differ in scope and leadership level.

What cities are hiring for Qc Stability Manager jobs? Cities with the most Qc Stability Manager job openings:
What are the most commonly searched types of Qc Stability jobs? The most popular types of Qc Stability jobs are:
What states have the most Qc Stability Manager jobs? States with the most job openings for Qc Stability Manager jobs include:
Director, QC Systems and Stability

Director, QC Systems and Stability

Biogen

NC • On-site

$178K - $245K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago

Biogen rating

9.2

Company rating: 9.2 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

3rd of 71 rated pharmaceutical

Job description

About This Role:
As the Director of Global QC Systems and Stability, you will be at the helm of a global quality control department that plays a critical role in supporting both manufacturing operations and release stability testing laboratories. Your leadership will guide the department in managing Contract Laboratory Management, Planning and Scheduling, QC Enterprise System Management (LIMS), Specification/Stability programs, and Reference Standards and Qualified Materials (RSMQ) Teams. Building strategic relationships with Site Quality Operations, key internal and external partners, IT, and Senior Leadership will be essential to support daily operations in both external and internal manufacturing environments.
You will harmonize and streamline processes, maintain SmartQC and LabWare LIMS, oversee global projects, and implement specifications and stability strategies for biologics, small molecules, and oligonucleotides products. You will also oversee a global team responsible for monitoring QC method performance, optimizing assay control trending, and managing Qualified Materials, Reference Standards, Critical Reagents, and cell-based materials essential for analytical testing.
This is a hybrid role to be based at our site in Research Triangle Park, NC or Cambridge, MA.
What You'll Do:
  • Identify, define, and drive strategy and improvement projects to maximize efficiency, streamline processes, and increase productivity in QC data, systems, and stability.
  • Staff senior-level QC personnel, ensuring their training and performance align with GMP compliant Quality Control operations.
  • Oversee the development and maintenance of budget plans for Contract Laboratory Operations OpEx (~$15-16MM).
  • Supervise activities at multiple Contract Laboratory Organizations (CLOs) supporting Biogen and Partner product testing, ensuring operational readiness.
  • Lead a team to acquire, qualify, and maintain reference standards and qualified materials for global laboratory operations.
  • Provide leadership and guidance to technical and operational staff in developing and implementing specification and stability strategies for various product modalities.
  • Utilize appropriate statistical tools to evaluate and interpret stability data, and guide the creation of stability reports and regulatory sections.
  • Serve as Business Process Owner (BPO) for Stability QMS and associated systems.
  • Perform other duties as assigned, contributing to the department's overall success.

Who You Are:
You are a strategic thinker with a robust background in quality control management. Your ability to build and maintain strategic relationships is complemented by your leadership skills in guiding technical and operational teams. You possess a keen analytical mind, capable of synthesizing complex data into actionable insights. Your interpersonal skills are strong, enabling you to operate effectively within a global, cross-functional environment. You thrive in a dynamic setting where you can drive efficiency and innovation.
Required Skills:
  • Bachelor's degree (Advanced degree preferred) in related field with at least 12 years of experience in the pharmaceutical industry, preferably within a scientific-related field.
  • Strong knowledge of regulatory, compliance, GMP, and laboratory testing, including troubleshooting and root cause investigations.
  • Comprehensive understanding of cGMPs, GLPs, and related global regulatory requirements.
  • Proven matrix leadership capability with effective verbal and written communication skills.
  • Strong analytical, critical thinking, and interpersonal skills.
  • Experience in utilizing statistical tools and methodologies to evaluate and interpret stability data.
  • Ability to synthesize technical information for senior management.

Job Level: Management
Additional Information
The base compensation range for this role is: $178,000.00-$245,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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About Biogen

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At Biogen, our mission is clear - we are pioneers in neuroscience. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. Together, our employees create, commercialize, and manufacture transformative therapies for our patient population.

Industry

Scientific research and development services

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

1978

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