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Quality Control Stability Jobs in Texas (NOW HIRING)

CYNET SYSTEMS

Spec 1, Quality Control

El Paso, TX · On-site

$21 - $26/hr

... finished products, and stability samples according to applicable procedures. * Collects ... and/or Quality Manager/Designee in order to achieve QC testing delivery goals. * Maintains ...

CYNET SYSTEMS

Quality Control Specialist I

El Paso, TX · On-site

$21 - $26/hr

... finished products, and stability samples according to applicable procedures. * Collects ... QC testing delivery goals. * Maintains Microbiology Lab audit readiness. Qualification And ...

Sovereign Pharmaceuticals

QC Chemist I

Fort Worth, TX · On-site

Analysis of in-process and finished drug products, including stability testing, for primarily high ... QC laboratory. * Compiles results as directed and understands basic concepts related to the ...

Sovereign Pharmaceuticals

QC Chemist I

Fort Worth, TX · On-site

Analysis of in-process and finished drug products, including stability testing, for primarily high ... QC laboratory. * Compiles results as directed and understands basic concepts related to the ...

AbbVie

QC Lab Supervisor II

Waco, TX · On-site

The QC Lab Supervisor II is responsible for the organization, administration, and supervision of ... stability samples. Organizes laboratory activity by coordinating the activity of personnel ...

Allergan

Supervisor II, QC Lab

Waco, TX · On-site

$85 - $115/hr

The QC Lab Supervisor II is responsible for the organization, administration, and supervision of ... stability samples. Organizes laboratory activity by coordinating the activity of personnel ...

New

Becton, Dickinson and Company

$23.50 - $30.75/hr

... QC testing delivery goals ... Performs microbiological testing on raw materials, in-process and finished products, and stability ...

Alcon

QC Microbiology Investigator (ASPEX)

Fort Worth, TX · On-site

$24.50 - $32/hr

As a QC Microbiology Investigator, supporting our QC, Analysis and Testing Service Team, you will ... stability samples in compliance with company standards and governmental regulatory requirements

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Quality Control Stability information

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 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 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 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.

Is quality control stability a good career choice?

Quality Control Stability is a role focused on maintaining product consistency and compliance through testing and monitoring processes. It often requires attention to detail, knowledge of industry standards, and proficiency with testing tools or software. This career can offer steady employment opportunities in manufacturing, pharmaceuticals, or food industries, with potential for advancement and certification.

Is quality control stability a good career path?

Quality control stability involves ensuring products meet quality standards over time, often requiring attention to detail and knowledge of testing procedures. It can offer steady employment and opportunities for advancement in manufacturing, pharmaceuticals, or food industries, especially for those with relevant certifications or experience. The career can be stable, but growth depends on industry demand and individual skill development.

What are the most commonly searched types of Quality Control Stability jobs in Texas?

The most popular types of Quality Control Stability jobs in Texas are:

What are popular job titles related to Quality Control Stability jobs in Texas?

For Quality Control Stability jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Quality Control Stability jobs in Texas look for?

The top searched job categories for Quality Control Stability jobs in Texas are:

What cities in Texas are hiring for Quality Control Stability jobs?

Cities in Texas with the most Quality Control Stability job openings:

Quality Control Stability jobs near you

Quality Control Project Lead - Cell Therapy

Lonza

Houston, TX • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 29 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

Job description

Quality Control Project Lead - Cell Therapy
Location: Houston, Texas - Onsite
Schedule: Monday-Friday, 8:00 AM-4:30 PM
As a Quality Control Project Lead, you will play a critical role in supporting late-stage cell therapy programs as they progress through Phase III, PPQ, and commercial launch activities. This position serves as the primary Quality Control representative for assigned client programs, partnering closely with QC laboratories, Program Management, Quality Assurance, Manufacturing, and customers to ensure successful technology transfers, analytical readiness, and project execution.
What you will get:
A competitive compensation package. In addition, below you will find a comprehensive summary of the benefits package we offer:
  • Performance-related bonus
  • Medical, dental and vision insurance
  • 401(k) matching plan
  • Life insurance, as well as short-term and long-term disability insurance
  • Employee assistance programs
  • Paid time off (PTO)

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What you will do:
  • Lead Quality Control activities supporting client programs through technology transfer, process development, qualification, validation, and commercial readiness efforts.
  • Serve as the primary QC representative on cross-functional project teams, communicating testing status, timelines, risks, and analytical requirements to internal stakeholders and customers.
  • Coordinate new product introductions and support implementation of new methods, assays, and processes within the QC organization.
  • Author, review, and approve technical documentation including transfer plans, assay transfer protocols, reports, specifications, sampling plans, stability reports, comparability reports, and bridging studies.
  • Collaborate with BioAnalytical Services and laboratory teams to support method qualification, validation, and analytical lifecycle management activities.
  • Provide technical support for investigations, deviations, out-of-specification events, CAPAs, audits, and regulatory compliance activities.
  • Support stability programs by coordinating protocol initiation, tracking testing milestones, and ensuring timely reporting of results and project deliverables.
  • Act as a liaison between customers and internal teams, ensuring expectations, commitments, and project timelines are effectively managed and communicated.

What we are looking for:
  • Bachelor's degree in a scientific discipline required.
  • Experience in Quality Control within a regulated biopharmaceutical, biotechnology, cell therapy, or related GMP environment.
  • Strong knowledge of cell therapy product development, technology transfer, analytical methods, validations, and product-specific qualification requirements.
  • Experience supporting new product introductions and cross-functional project execution.
  • Demonstrated technical writing experience, including preparation and review of scientific reports and GMP documentation.
  • Customer-facing experience with the ability to effectively manage client relationships and stakeholder communications.
  • Strong organizational, planning, and project management capabilities with proven ability to manage multiple priorities simultaneously.
  • Experience with analytical techniques such as flow cytometry, ELISA, PCR, cell viability, or cell-based assays preferred.
  • Excellent verbal and written communication skills, attention to detail, and ability to influence cross-functional teams.

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.
Ready to shape the future of life sciences? Apply now.

What Lonza employees say

Pay

Benefits

Hours and flexibility

Workplace

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US

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